Fat Loss

Research compounds studied for their role in appetite regulation, lipolysis, and metabolic function. Includes GLP-1 agonists, GH fragments, and GH secretagogues.

Most researched for Fat Loss

Semaglutide

The most extensively studied compound in this category with the largest clinical trial dataset. A GLP-1 receptor agonist that reduces appetite by slowing gastric emptying and signaling satiety to the brain. Weekly dosing and distinct mechanism from other compounds here make it the most commonly referenced starting point.

Ibutamoren

aka MK-677, MK-677, Nutrobal, MK-0677

Popular

How it works: An oral compound that signals your body to release more of its own growth hormone, studied for muscle growth, recovery, and deeper sleep.

GH and IGF-1 elevation; muscle mass; recovery; sleep quality; anti-aging

Research dose

10-25 mg, Once daily (oral)

Real-world (reported)

10–25 mg nightly. Many prefer 10–12.5 mg long-term. 5 on/2 off used by some.

Administration

Oral

Timing

Evening (aligns with GH pulse and sleep)

Cycle length

8–12 wks on; 4–8 wks off; long-term use debated

Real-world figures are community-reported, not medical advice.

Common side effects: Increased appetite (strong); water retention; fatigue first 2 wks; mild joint pain

Community take: [ANECDOTAL] Very widely used. Sleep improvement and vivid dreams. 10 mg preferred for fewer sides.

Onset
Appetite increase within days; body composition 8+ wks
Half-life
~24h
Storage
Dry: Room temp; dry; away from heat/moisture
Reconstitution
N/A (oral)
Rare side effects
Insulin resistance/glucose elevation (significant at 25 mg); theoretical tumor risk
Contraindications
Type 2 diabetes or insulin resistance; active malignancy; pregnancy; History of or risk factors for congestive heart failure (identified safety signa; Diabetes mellitus or prediabetes (MK-677 increases fasting glucose and reduces i; Active malignancy or history of cancer (elevated IGF-1 may promote tumor growth); Not approved for human use; investigational compound onlyFrequency distribution
Drug interactions
Insulin/antidiabetics (glucose monitoring); CNS depressants (additive sedation)
Recommended bloodwork
IGF-1 (baseline + 4–8 wks); fasting glucose; HbA1c; fasting insulin
Stacks well with
CJC-1295+Ipamorelin: triple GH stimulation (monitor IGF-1). BPC-157: recovery stack.
Secondary uses
Bone density; fat loss; cognitive function; skin quality
Research status
Multiple Phase 2 human trials; no FDA approval; investigational drug status
FDA status
No
Legal status
US: Not FDA-approved; investigational drug; sold as research chemical · UK: Legal to import as research chemical · Canada: Legal research chemical · Australia: Schedule 4 · EU: Research chemical most EU
Typical price
$30–$70 / month supply
Research evidence
moderate
Indications
Growth hormone deficiency (investigational); Age-related sarcopenia and frailty (investigational); Bone density and osteoporosis research; Body composition improvement in elderly populations
Chemical data
CAS 159634-47-6 · C27H36N4O5S · 528.67 Da
Amino acids
51 aa

Semaglutide

aka Ozempic, Wegovy, Rybelsus

PopularApproved

How it works: Mimics GLP-1 hormone to slow gastric emptying and reduce appetite signals in the brain.

Type 2 diabetes (Ozempic); chronic weight management (Wegovy)

Research dose

0.25-2.4 mg, Once weekly (SubQ); Rybelsus: 3–14 mg oral daily

Real-world (reported)

Titration: 0.25 mg wk 1–4, 0.5 mg wk 5–8, increase per tolerance

Administration

SubQ (Ozempic/Wegovy); Oral (Rybelsus)

Timing

Once weekly (SubQ); morning 30 min before food (oral)

Cycle length

Chronic; titration: 0.25 mg ×4 wk → 0.5 → 1 → 1.7 → 2.4 mg

Real-world figures are community-reported, not medical advice.

Common side effects: Nausea (30–50%); vomiting; diarrhea; constipation; injection-site reactions

Community take: [ANECDOTAL] Most discussed weight-loss peptide 2023–2026. Titration: 0.25 mg → increase per tolerance.

Onset
Appetite suppression 1 wk; weight loss 8–16 wks
Half-life
~7 days
Storage
Dry: Refrigerate 2–8°C; do not freeze auto-injectors; in-use pen: room temp ≤56 days · Reconstituted: Compounded: 28 days refrigerated
Reconstitution
Verify mg/mL carefully for compounded versions
Rare side effects
Pancreatitis; gallstones; gastroparesis; thyroid C-cell tumors (black box — animal data); suicidal ideation (rare reports)
Contraindications
MEN2 / medullary thyroid cancer history; pancreatitis; pregnancy; Personal or family history of medullary thyroid carcinoma (MTC) or Multiple Endo; Pregnancy (may cause fetal harm; discontinue at least 2 months before planned co; Prior serious hypersensitivity reaction to semaglutide or any excipient; History of pancreatitis (use with caution; not an absolute contraindication per
Drug interactions
Insulin/sulfonylureas (hypoglycemia); oral drugs (gastric emptying delay)
Recommended bloodwork
HbA1c; fasting glucose; lipid panel; weight; BP; eGFR; thyroid if concerned; amylase/lipase if symptoms
Stacks well with
Cagrilintide: Phase 3 CagriSema combo. Metformin: commonly co-prescribed. Do NOT combine with other GLP-1 agonists.
Secondary uses
CV risk reduction; NASH/NAFLD; renal protection; addiction treatment (emerging)
Research status
FDA-approved; SUSTAIN (T2D) and STEP (obesity) Phase 3 trials; SELECT 2023 (CV risk)
FDA status
Yes (Ozempic T2D; Wegovy obesity)
Legal status
US: FDA-approved Ozempic/Wegovy. Compounded: 50+ FDA warning letters Sept 2025; mostly prohibited now · UK: Prescription-only; NHS coverage some cases · Canada: Prescription-only under Health Canada · Australia: TGA-approved (Ozempic, Wegovy) · EU: EMA-approved; prescription across EU
Typical price
Brand $800–$1,200/month (US without insurance)
Research evidence
high
Indications
Type 2 diabetes glycemic control; Chronic weight management in adults with obesity or overweight; Cardiovascular risk reduction in overweight/obese adults
Chemical data
CAS 910463-68-2 · C187H291N45O59 · 4113.58 Da
Amino acids
2666 aa

Tirzepatide

aka GIP/GLP-1 receptor agonist, dual GIP/GLP-1 agonist, Mounjaro, Zepbound

PopularApproved

How it works: Dual GIP/GLP-1 receptor activation reduces appetite and improves glucose control while modulating CNS behavior pathways.

Weight management, metabolic control, behavioral dysregulation in neurodevelopmental disorders

Research dose

5-5 mg, Weekly

Real-world (reported)

Same titration as Ozempic. Community max tolerated often 5–10 mg (full 15 mg significant GI burden).

Administration

Injection

Timing

Once weekly any time

Cycle length

Chronic; titration: 2.5 mg ×4 wk; +2.5 mg q4wk to max 15 mg

Real-world figures are community-reported, not medical advice.

Common side effects: Well tolerated (specific adverse events not detailed in case report)

Community take: This case report suggests tirzepatide may have therapeutic potential beyond standard weight management, particularly in rare neurodevelopmental disorders with behavioral and metabolic phenotypes like Smith-Magenis syndrome.

Onset
10 months for measurable weight loss and behavioral improvement
Half-life
~5 days
Storage
Dry: Refrigerate 2–8°C; room temp ≤30°C up to 21 days in-use; do not freeze
Reconstitution
N/A (auto-injector)
Rare side effects
Pancreatitis; gallstones; thyroid C-cell tumors (black box — animal); gastroparesis; tachycardia (HR increase in trials)
Contraindications
MEN2/medullary thyroid history; pancreatitis; pregnancy; Personal or family history of medullary thyroid carcinoma (MTC) or Multiple Endo; Pregnancy (may cause fetal harm based on animal data; discontinue at least 2 mon; Prior serious hypersensitivity reaction to tirzepatide or any excipient; History of pancreatitis (use with caution; not an absolute contraindication per
Drug interactions
Insulin/sulfonylureas (hypoglycemia); oral drug absorption affected by gastric emptying
Recommended bloodwork
HbA1c; fasting glucose; lipid panel; weight; BP; HR; eGFR; amylase/lipase if symptoms
Stacks well with
Cagrilintide: Phase 3 combo (active). Metformin: common co-prescription. Do NOT combine with semaglutide.
Secondary uses
Fasting glucose reduction, aggression reduction, food-seeking behavior control
Research status
Clinical case report; FDA approved for weight management in general population
FDA status
Yes (Mounjaro T2D; Zepbound obesity)
Legal status
US: FDA-approved (Mounjaro, Zepbound). Compounded: FDA enforcement mirrors semaglutide — mostly prohibited. · UK: Prescription-only; NICE approved some cases · Canada: Prescription-only under Health Canada · Australia: TGA-approved (Mounjaro; Zepbound approval underway) · EU: EMA-approved (Mounjaro)
Typical price
Brand $1,000–$1,300/month (US without insurance)
Research evidence
high
Indications
Type 2 diabetes glycemic control; Chronic weight management in adults with obesity or overweight; Cardiovascular risk reduction in obesity (under investigation)
Chemical data
CAS 2023788-19-2 · C225H348N48O68 · 4813.45 Da
Amino acids
2069 aa

Liraglutide

aka Victoza, Saxenda, NN2211

PopularApproved

How it works: A daily GLP-1 medication and the predecessor to semaglutide, which slows digestion and reduces appetite for weight loss and blood-sugar control.

Type 2 diabetes (Victoza); obesity/weight management (Saxenda)

Research dose

0.6-3 mg, Once daily (SubQ); titrate over 5 weeks

Real-world (reported)

Titrate: 0.6 mg/day wk 1; 1.2 mg wk 2; 1.8 mg wk 3; 2.4 mg wk 4; 3.0 mg wk 5+.

Administration

SubQ

Timing

Once daily any time (consistent)

Cycle length

Chronic maintenance

Real-world figures are community-reported, not medical advice.

Common side effects: Nausea (very common); vomiting; diarrhea; constipation; injection-site reactions

Community take: [ANECDOTAL] Largely superseded by semaglutide and tirzepatide for weight loss. Still used when weekly injections are not tolerated. Daily dosing inconvenience is main complaint.

Onset
GI effects 1 wk; weight loss 8–16 wks
Half-life
~13h
Storage
Dry: Refrigerate 2–8°C; room temp up to 30 days in-use; do not freeze · Reconstituted: N/A (pen discarded after use)
Reconstitution
N/A (pre-filled pen)
Rare side effects
Pancreatitis; gallstones; thyroid C-cell tumors (black box); gastroparesis
Contraindications
MEN2/medullary thyroid history; pancreatitis history; pregnancy; Personal or family history of medullary thyroid carcinoma (MTC) or Multiple Endo; Prior serious hypersensitivity reaction to liraglutide or any excipient; Pregnancy (Category X); Do not use with other GLP-1 receptor agonists (e.g.; semaglutide; exenatide; tir
Drug interactions
Insulin/sulfonylureas (hypoglycemia); oral drug absorption (gastric emptying)
Recommended bloodwork
HbA1c; fasting glucose; weight; BP; eGFR; lipid panel; amylase/lipase if symptoms
Stacks well with
Semaglutide: more potent alternative (weekly). Tirzepatide: dual agonist alternative.
Secondary uses
CV risk reduction; NASH; renal protection
Research status
FDA-approved Phase 3 SCALE and LEADER trials
FDA status
Yes (Victoza T2D; Saxenda obesity)
Legal status
US: FDA-approved (Victoza, Saxenda) · UK: Prescription-only; NICE approved · Canada: Prescription-only (Health Canada) · Australia: TGA-approved · EU: EMA-approved
Typical price
Brand ~$500–$900/month (Saxenda US without insurance)
Research evidence
high
Indications
Type 2 diabetes glycemic control; Chronic weight management in adults with obesity or overweight; Adolescent obesity (ages 12-17); Cardiovascular risk reduction in T2D patients
Chemical data
CAS 204656-20-2 · C172H265N43O51 · 3751.2 Da
Amino acids
2671 aa

AOD-9604

aka hGH Frag 177-191, Anti-Obesity Drug 9604, hGH Fragment 176-191

ModeratePreclinical

How it works: Mimics the fat-metabolizing region of growth hormone without affecting insulin or blood glucose.

Fat loss; lipolysis; metabolic enhancement

Research dose

250-500 mcg, Once daily AM fasted

Real-world (reported)

300 mcg SubQ fasted AM daily. Local injection near stubborn fat deposits used by some.

Administration

SubQ

Timing

Morning fasted 30 min before food

Cycle length

12–16 weeks

Real-world figures are community-reported, not medical advice.

Common side effects: Generally mild; mild injection-site reactions; headache (rare)

Community take: [ANECDOTAL] Popular in Australian market (TGA cosmetic listing). Results often modest. Weaker than GLP-1s for meaningful fat loss.

Onset
Acute lipolysis within days; cumulative fat loss weeks
Half-life
<1h
Storage
Dry: Fridge 2–8°C; freeze >6 mo · Reconstituted: Refrigerate; use within 28 days
Reconstitution
Add 2 mL BAC water to 5 mg vial = 2.5 mg/mL; 500 mcg = 20 IU
Rare side effects
Modern trials showed modest/disappointing weight loss efficacy; safety profile excellent
Contraindications
Active malignancy; pregnancy; Active malignancy or history of cancer (theoretical concern due to hGH derivatio; Pregnancy or breastfeeding (no reproductive safety data available); Hypersensitivity to AOD-9604 or any formulation components; Children and adolescents (no pediatric safety data)Frequency distribution of rep
Drug interactions
No significant documented interactions
Recommended bloodwork
Fasting glucose; lipid panel; body composition
Stacks well with
CJC-1295+Ipa: recomp stack. Tesofensine: fat-loss stack.
Secondary uses
Anti-obesity; potential cartilage/bone effects (emerging)
Research status
Australian clinical trials (Phase 2/3 by Metabolic Pharmaceuticals ~2006); FDA Phase 2 complete; no approval; TGA cosmetic listed
FDA status
No (TGA cosmetic listed — Australia)
Legal status
US: Not FDA-approved; research chemical · UK: Legal for research · Canada: Legal research chemical · Australia: TGA cosmetic listing = semi-legal in Australia (unique status) · EU: Varies by EU member state
Typical price
$25–$50 / 5 mg vial
Research evidence
moderate
Indications
Fat metabolism and lipolysis research; Obesity and weight management studies; Cartilage and joint repair research; Growth hormone fragment pharmacology; Metabolic syndrome research
Chemical data
CAS 221231-10-3 · C78H123N23O23S2 · 1815.12 Da
Amino acids
63 aa

Sermorelin Acetate

aka Sermorelin, GHRH(1-29), GRF 1-29

ModerateApproved

How it works: Prompts the pituitary to release your own growth hormone in a natural pulse, studied for body composition, recovery, and sleep.

GH stimulation; body composition; sleep; anti-aging (clinic use)

Research dose

100-500 mcg, Once daily pre-bed

Real-world (reported)

200–300 mcg pre-bed SubQ. Stack with ipamorelin 200 mcg for synergy.

Administration

SubQ

Timing

Pre-bed on empty stomach

Cycle length

8–16 weeks

Real-world figures are community-reported, not medical advice.

Common side effects: Mild flushing/head rush; injection-site reactions; water retention

Community take: [ANECDOTAL] Considered the 'classic' GHRH; less potent than CJC-1295 no DAC but well-tolerated. Often first Rx GH peptide prescribed by clinics.

Onset
GH pulse 30 min; body composition weeks–months
Half-life
~10–20 min
Storage
Dry: Fridge 2–8°C; freeze long-term · Reconstituted: Refrigerate; use within 28 days
Reconstitution
Add 2 mL BAC water to 3 mg vial = 1.5 mg/mL; 100 mcg = ~6.7 IU
Rare side effects
Joint pain at high doses; blood sugar changes
Contraindications
Active malignancy; pregnancy; hypothyroidism (treat first); Active malignancy or history of cancer (GH-dependent tumors); Hypersensitivity to sermorelin or GHRH analogs; Acute critical illness (GH may worsen outcomes in critically ill patients); Active proliferative diabetic retinopathy
Drug interactions
Glucocorticoids blunt response
Recommended bloodwork
IGF-1 (baseline + 4–8 wks); fasting glucose
Stacks well with
Ipamorelin: recommended combination. Less potent than Mod GRF 1-29 but well-studied.
Secondary uses
IGF-1 elevation; muscle preservation; skin quality
Research status
Was FDA-approved (Geref, withdrawn 2008 by manufacturer); widely used in compounding practice; human data solid
FDA status
No (Rx compounded)
Legal status
US: Not FDA-approved (Geref withdrawn); compounding legal; gray-market research chemical · UK: Legal for research; Rx compounding available · Canada: Legal research chemical or Rx · Australia: Schedule 4 (Rx) · EU: Varies by member state
Typical price
$30–$60 / 3 mg vial
Research evidence
moderate
Indications
Growth hormone deficiency diagnostic testing; Anti-aging and regenerative medicine research; GH secretion stimulation studies; Combined GHRH/GHRP protocol investigations
Chemical data
CAS 86168-78-7 · C149H246N44O42S · 3357.88 Da
Amino acids
235 aa

Tesamorelin

aka Egrifta, TH9507, Tesamorelin Acetate

ModerateApproved

How it works: A GHRH analog with FDA approval for visceral fat reduction in HIV-associated lipodystrophy.

Visceral fat reduction (FDA-approved HIV lipodystrophy); GH/IGF-1 elevation; body composition

Research dose

1-2 mg, Once daily SubQ

Real-world (reported)

1–2 mg SubQ daily in morning. Anti-aging clinics often use 1 mg/day. Gray-market users often prefer cheaper CJC-1295.

Administration

SubQ

Timing

Morning before breakfast preferred

Cycle length

12–16 weeks (FDA protocol); off-label: longer

Real-world figures are community-reported, not medical advice.

Common side effects: Flushing; injection-site reactions; arthralgia; edema; paresthesia

Community take: [ANECDOTAL] Highly regarded in anti-aging clinic setting for visceral fat. More expensive than CJC-1295 but FDA-validated for VAT reduction.

Onset
IGF-1 rise within 2 wks; visceral fat reduction 8–12 wks
Half-life
~26–38 min
Storage
Dry: Fridge 2–8°C; do not freeze; protect from light · Reconstituted: Refrigerate; use within 28 days; discard if cloudy
Reconstitution
Add 2.2 mL sterile water (kit) or BAC water to 1 mg vial = ~0.5 mg/mL; 1 mg dose = ~2 mL
Rare side effects
Glucose elevation; IGF-1 elevation beyond normal range at high dose; possible malignancy promotion (theoretical)
Contraindications
Active malignancy; pregnancy; hypothalamic/pituitary tumor; disrupted HPA axis; Active malignancy (GH may promote tumor growth); Pregnancy (Category X based on animal reproduction studies); Disruption of hypothalamic-pituitary axis due to hypophysectomy; hypopituitarism; Known hypersensitivity to tesamorelin or mannitolFrequency distribution of repor
Drug interactions
Glucocorticoids; cytochrome P450 substrates (modest effect via GH)
Recommended bloodwork
IGF-1 (every 3 mo); fasting glucose; HbA1c; waist circumference; lipid panel
Stacks well with
Ipamorelin: GH axis stack. CJC-1295 no DAC: alternative or complementary GHRH.
Secondary uses
Anti-aging; muscle preservation; cognitive function (emerging data)
Research status
FDA-approved Phase 3 LIPO trials; additional data on cognitive function in HIV patients
FDA status
Yes (Egrifta — HIV lipodystrophy)
Legal status
US: FDA-approved (HIV lipodystrophy only); off-label compounding available · UK: Prescription-only · Canada: Prescription-only (Health Canada) · Australia: Schedule 4 (Rx) · EU: EMA-approved limited indication
Typical price
$80–$150 / 1 mg vial (brand Egrifta very expensive)
Research evidence
high
Indications
HIV-associated lipodystrophy treatment; Visceral fat reduction; Growth hormone deficiency research; Cognitive function research (NASH trials)
Chemical data
CAS 218949-48-5 · C221H366N72O67S1 · 5135.9 Da
Amino acids
2203 aa

GHRP-2

aka Pralmorelin, KP-102, Growth Hormone Releasing Peptide-2

ModerateApproved

How it works: Triggers a strong pulse of your own growth hormone for body composition and recovery, though it also nudges up cortisol and prolactin.

Strong GH pulse stimulation; body composition; recovery

Research dose

100-300 mcg, 1–3×/day

Real-world (reported)

100–200 mcg pre-bed or pre-workout. Stack with Mod GRF 1-29. Monitor mood (cortisol).

Administration

SubQ / IM

Timing

Pre-bed or pre-workout

Cycle length

8–12 wks on; 4 wks off

Real-world figures are community-reported, not medical advice.

Common side effects: Head rush; flushing; cortisol/prolactin bump; increased hunger; injection-site reactions

Community take: [ANECDOTAL] Strong GH release but cortisol/prolactin spike makes it less popular than ipamorelin. Used by more experienced users who want stronger GH stimulus.

Onset
GH pulse within 30 min; body composition weeks
Half-life
~30 min
Storage
Dry: Fridge 2–8°C; freeze long-term · Reconstituted: Refrigerate; use within 28 days
Reconstitution
Add 2 mL BAC water to 2 mg vial = 1 mg/mL; 100 mcg = 10 IU
Rare side effects
Significant cortisol elevation (stress hormone concern long-term); prolactin elevation
Contraindications
Active malignancy; depression (cortisol); pregnancy; prolactin-sensitive conditions; Pituitary tumors (risk of stimulating tumor growth through GH axis activation); Active cancer (theoretical risk from chronic GH/IGF-1 axis stimulation); Pregnancy (no safety data available in pregnant women)Frequency distribution of; GH/IGF-1 axis drugs (recombinant GH; IGF-1; GHRH analogs) - potential for additi
Drug interactions
Glucocorticoids; aromatase inhibitors; prolactin-modulating drugs
Recommended bloodwork
IGF-1; cortisol (morning); prolactin; fasting glucose
Stacks well with
CJC-1295 no DAC: standard GHRH pair. Less preferred than ipamorelin due to cortisol/prolactin.
Secondary uses
IGF-1 elevation; healing; muscle mass
Research status
Preclinical robust; human clinical trial data as Pralmorelin (Japan); compounding protocols
FDA status
No
Legal status
US: Research use only · UK: Legal for research · Canada: Legal research chemical · Australia: Schedule 4 · EU: Unregulated
Typical price
$20–$40 / 2 mg vial
Research evidence
moderate
Indications
GH deficiency diagnosis (approved in Japan); Growth hormone research; Appetite stimulation studies; Neuroendocrine function testing
Chemical data
CAS 158861-67-7 · C45H55N9O6 · 817.9 Da
Amino acids
235 aa

hGH Fragment 176-191

aka hGH Frag 176-191, AOD hGH frag, AOD-9604

ModeratePreclinical

How it works: Isolates the lipolytic region of growth hormone, promoting fat breakdown without IGF-1 stimulation.

Fat loss; lipolysis; anti-obesity

Research dose

250-500 mcg, Once daily AM fasted

Real-world (reported)

300–500 mcg SubQ fasted AM daily.

Administration

SubQ

Timing

Morning fasted 30 min before food

Cycle length

12–16 wks

Real-world figures are community-reported, not medical advice.

Common side effects: Generally mild; injection-site reactions; headache (rare)

Community take: [ANECDOTAL] Popular in Australian market. Results modest vs GLP-1 alternatives. Local injection into fat areas used by some.

Onset
Acute lipolysis within days; body composition weeks
Half-life
<1h
Storage
Dry: Fridge 2–8°C; freeze long-term · Reconstituted: Refrigerate; use within 28 days
Reconstitution
Add 2 mL BAC water to 5 mg vial = 2.5 mg/mL; 500 mcg = 20 IU
Rare side effects
Phase 2 results modest; limited long-term data
Contraindications
Active malignancy; pregnancy; Pregnancy and lactation (no reproductive safety data available); Active malignancy (precautionary; insufficient long-term oncogenicity data); Known hypersensitivity to AOD-9604 or formulation componentsFrequency distributi; Insulin and sulfonylureas: theoretical additive glycemic effects; monitor glucos
Drug interactions
No significant interactions
Recommended bloodwork
Fasting glucose; lipid panel; body composition
Stacks well with
CJC-1295+Ipamorelin: GH recomp stack.
Secondary uses
Bone density (some data); cartilage repair (limited)
Research status
Preclinical robust; Phase 2 human data (Metabolic Pharmaceuticals); TGA cosmetic listed in Australia
FDA status
No
Legal status
US: Not FDA-approved; research chemical · UK: Legal for research · Canada: Legal research chemical · Australia: TGA cosmetic listed — unique semi-legal status AU · EU: Varies by EU state
Typical price
$25–$50 / 5 mg vial
Research evidence
low
Indications
Fat metabolism and lipolysis research; Anti-obesity peptide investigations; Metabolic syndrome research; Body composition studies
Chemical data
CAS 221231-10-3 · C78H125N23O23S2 · 1817.12 Da
Amino acids
16 aa

CJC-1295 with DAC

aka CJC-1295 DAC, Drug Affinity Complex CJC-1295, Modified GRF(1-29) with DAC

ModeratePhase 2

How it works: A long-acting growth-hormone booster that keeps GH and IGF-1 elevated for days from one dose, studied for body composition and anti-aging.

Sustained GH/IGF-1 elevation; body composition; anti-aging; less frequent dosing

Research dose

1-2 mg, Once or twice per week

Real-world (reported)

1–2 mg SubQ 1–2×/week. Less popular than no-DAC version in community.

Administration

SubQ

Timing

Any time (long half-life)

Cycle length

8–12 weeks

Real-world figures are community-reported, not medical advice.

Common side effects: Fluid retention; numbness/tingling; water retention; flushing (less acute than pulsatile)

Community take: [ANECDOTAL] Convenient (once or twice weekly). However community has moved toward CJC-1295 no DAC for more physiological pulsatile profile. 'Blunts natural rhythm.'

Onset
GH/IGF-1 elevation within days; sustained; body composition weeks–months
Half-life
~6–8 days
Storage
Dry: Fridge 2–8°C; freeze long-term · Reconstituted: Refrigerate; use within 28 days
Reconstitution
Add 2 mL BAC water to 2 mg vial = 1 mg/mL; 1 mg dose = 100 IU
Rare side effects
IGF-1 elevation beyond normal range (tonic elevation risk); tumor promotion (theoretical); joint pain
Contraindications
Active malignancy; pregnancy; hypothyroidism; Active malignancy or history of cancer (GH/IGF-1 may promote tumor growth); Pregnancy and breastfeeding (no safety data); Known hypersensitivity to CJC-1295 or any excipients; Uncontrolled diabetes (GH elevation may worsen glucose tolerance)
Drug interactions
Glucocorticoids; insulin
Recommended bloodwork
IGF-1 (baseline + every 4–6 wks; more important than with short-acting); fasting glucose; thyroid
Stacks well with
Does NOT need to be stacked with GHRP as urgently as no-DAC. Some stack with ipamorelin for added pulse.
Secondary uses
Muscle preservation; fat loss; sleep quality
Research status
Preclinical; human compounding clinical use; some concern about tonic vs pulsatile GH regarding safety
FDA status
No
Legal status
US: Research use only · UK: Legal for research · Canada: Legal research chemical · Australia: Schedule 4 · EU: Unregulated
Typical price
$30–$70 / 2 mg vial
Research evidence
moderate
Indications
Growth hormone deficiency research; Age-related GH decline investigation; Body composition research; Anti-aging and longevity research
Chemical data
CAS 863288-34-0 · C165H271N47O46 · 3647.28 Da
Amino acids
38 aa

5-Amino-1MQ

aka 5-Amino-1-methylquinolinium, 5A1MQ, NNMTi

ModeratePreclinical

How it works: Blocks an enzyme (NNMT) that slows metabolism, helping fat cells burn energy instead of storing it - studied for fat loss, especially belly fat.

Fat loss (particularly visceral); metabolic rate increase; NAD+ pathway support

Research dose

50-150 mg, Once daily (oral)

Real-world (reported)

50–100 mg oral daily. Some stack with NAD+ precursors (NMN/NR).

Administration

Oral

Timing

Any time

Cycle length

8–12 weeks

Real-world figures are community-reported, not medical advice.

Common side effects: Limited human data: fatigue (rare); GI upset (mild); headache

Community take: [ANECDOTAL – biohacker community] Reports of meaningful fat loss especially visceral fat. 'Works where diet alone fails.' Limited community size vs mainstream peptides.

Onset
Energy increase within days; body composition changes 8+ wks
Half-life
~6h estimated
Storage
Dry: Room temperature; dry
Reconstitution
N/A (oral)
Rare side effects
No human safety data; unknown long-term effects
Contraindications
Active malignancy; pregnancy; No formal contraindications established (no human studies); Theoretical concern for individuals with NNMT-dependent cancers; Theoretical concern for pregnancy/lactation (no reproductive toxicity data)Frequ; No drug interaction studies have been conducted
Drug interactions
Limited interaction data
Recommended bloodwork
Fasting glucose; HbA1c; body composition; lipid panel; NAD+ levels (research context)
Stacks well with
MOTS-c: metabolic synergy (AMPK activation + NNMT inhibition). Tesofensine: fat-loss stack.
Secondary uses
Muscle mass preservation; insulin sensitivity; longevity (emerging)
Research status
Preclinical animal data (obesity models); no published human clinical trials as of 2026; gray-market community use
FDA status
No
Legal status
US: Research use only; not FDA-approved · UK: Legal for research · Canada: Legal research chemical · Australia: Schedule 4 · EU: Unregulated
Typical price
$30–$80 / month supply
Research evidence
low
Indications
Metabolic research (obesity and adipocyte biology); NAD+ pathway modulation research; Sarcopenia and muscle aging research; NNMT biology investigation
Chemical data
CAS 42464-96-0 · C10H11N2+ · 159.21 Da
Amino acids
46 aa

Tesofensine

aka NS2330, TE-0911, Tesofen

ModeratePhase 3

How it works: A brain-acting compound that raises dopamine, norepinephrine, and serotonin to strongly curb appetite and lift metabolism.

Significant weight loss via appetite suppression and metabolic rate increase

Research dose

0.25-1 mg, Once daily (oral)

Real-world (reported)

0.25–0.5 mg oral daily. Start low. Monitor BP and HR closely. Morning dosing only (insomnia risk).

Administration

Oral

Timing

Morning

Cycle length

12–24 weeks

Real-world figures are community-reported, not medical advice.

Common side effects: Dry mouth; nausea; constipation; insomnia; elevated heart rate; increased BP (significant); palpitations

Community take: [ANECDOTAL] Effective for weight loss but cardiovascular effects are real concern. 'Works well but watch your heart rate.' Community consensus: not a starter compound.

Onset
Appetite reduction within days; weight loss 4–8 wks
Half-life
~9 days
Storage
Dry: Room temperature; dry
Reconstitution
N/A (oral)
Rare side effects
Significant cardiovascular effects (tachycardia, hypertension); abuse potential (dopaminergic); serotonin syndrome (with serotonergic drugs)
Contraindications
Cardiovascular disease; hypertension; arrhythmia; hyperthyroidism; MAOIs; pregnancy; psychiatric disorders; Concurrent use of monoamine oxidase inhibitors (MAOIs) - serotonin syndrome risk; Concurrent use of other serotonergic agents (SSRIs; SNRIs; triptans; tramadol) w; Uncontrolled hypertension; Recent (less than 6 months) myocardial infarction or unstable angina
Drug interactions
MAOIs (serotonin syndrome); SSRIs/SNRIs; stimulants (additive); antihypertensives (counteracted)
Recommended bloodwork
HR and BP (every 2–4 weeks); ECG baseline; weight; fasting glucose
Stacks well with
GLP-1 agonists: different mechanism; may combine cautiously (monitor CV carefully). 5-Amino-1MQ: metabolic stack.
Secondary uses
Potential Parkinson's adjunct; ADHD (off-label exploration)
Research status
Phase 2 human trials for obesity (Astrup et al. 2008 Lancet); Phase 3 initiated; approved in Brazil 2025; not FDA-approved
FDA status
No
Legal status
US: Not FDA-approved; research chemical; approved Brazil 2025 · UK: Legal for research · Canada: Legal research chemical · Australia: Schedule 4 · EU: Approved Brazil; research chemical in most EU
Typical price
$50–$150 / month supply
Research evidence
moderate
Indications
Investigational treatment for obesity (late-stage clinical development); Previously investigated in Parkinson's disease (discontinued); Previously investigated in Alzheimer's disease (discontinued)
Chemical data
CAS 195875-84-4 · C17H26Cl2N2 · 327.85 g/mol
Amino acids
31 aa

Orforglipron

aka LY3502970, OWL-833

ModeratePhase 3

How it works: An oral once-daily GLP-1 pill that curbs appetite through the same pathway as semaglutide, without injections.

Obesity; T2D — without injection

Research dose

12-120 mg, Once daily (oral)

Real-world (reported)

Phase 3 dosing only — no established gray-market protocol.

Administration

Oral

Timing

Once daily with or without food

Cycle length

Chronic; titration per protocol

Real-world figures are community-reported, not medical advice.

Common side effects: Nausea; vomiting; diarrhea; constipation (GLP-1 class effect)

Community take: [ANECDOTAL] Very limited gray-market. Phase 2 data drives interest. Oral convenience is key differentiator vs injectable semaglutide.

Onset
GI effects within days; weight loss 8–16 wks
Half-life
~12h
Storage
Dry: Room temperature; dry
Reconstitution
N/A (oral)
Rare side effects
Pancreatitis; gallstones; thyroid C-cell tumors (GLP-1 class black box)
Contraindications
MEN2/medullary thyroid history; pancreatitis; pregnancy; Personal or family history of medullary thyroid carcinoma (MTC) or Multiple Endo; Pregnancy (potential fetal harm based on GLP-1 agonist class data); Prior serious hypersensitivity reaction to orforglipron or excipientsFrequency d; Insulin and sulfonylureas: Potential increased risk of hypoglycemia when combine
Drug interactions
Oral drug absorption delay; insulin/antidiabetics
Recommended bloodwork
HbA1c; fasting glucose; weight; GI symptoms; amylase/lipase
Stacks well with
Not combined with injectable GLP-1 agonists. Metformin: common co-treatment in trials.
Secondary uses
CV risk reduction; NAFLD; reduced access barriers vs injectable GLP-1s
Research status
Phase 3 trials ongoing (Eli Lilly); Phase 2 NEJM 2023 (14.7% weight loss at 36 wks, 45 mg); no FDA approval yet
FDA status
No
Legal status
US: Not FDA-approved; investigational; gray-market research chemical · UK: Legal for research · Canada: Legal research chemical · Australia: Not TGA-approved · EU: Not EMA-approved
Typical price
Variable / limited
Research evidence
high
Indications
Weight management in adults with obesity or overweight; Type 2 diabetes glycemic control; Cardiometabolic risk factor improvement
Chemical data
CAS 2212020-52-3 · C48H48F2N10O5 · 883 Da
Amino acids
77 aa

Mazdutide

aka IBI362, LY3305677, OXM-3

ModerateApproved

How it works: A weekly fat-loss compound that hits both the GLP-1 appetite pathway and the glucagon pathway, adding extra calorie burn and liver-fat mobilization.

Obesity; metabolic syndrome; NAFLD/NASH; weight loss

Research dose

2-9 mg, Once weekly (SubQ)

Real-world (reported)

2–9 mg weekly per Phase 3 protocol. Very limited community protocols.

Administration

SubQ

Timing

Once weekly any time

Cycle length

Titration per protocol

Real-world figures are community-reported, not medical advice.

Common side effects: Nausea; vomiting; diarrhea; injection-site reactions

Community take: [ANECDOTAL] Primarily Chinese gray-market. Limited Western experience. 'Retatrutide without GIP' shorthand.

Onset
GI effects within days; weight loss 8–16 wks
Half-life
~5–7 days
Storage
Dry: Fridge 2–8°C · Reconstituted: Refrigerate; use within 28 days
Reconstitution
Verify mg/mL from vendor
Rare side effects
Pancreatitis; thyroid C-cell (class); gallstones
Contraindications
MEN2/thyroid history; pancreatitis; pregnancy; Personal or family history of medullary thyroid carcinoma (MTC); Multiple endocrine neoplasia syndrome type 2 (MEN 2); Known hypersensitivity to mazdutide or excipients; Pregnancy and breastfeeding
Drug interactions
Insulin/antidiabetics; do not combine with other GLP-1 agonists
Recommended bloodwork
HbA1c; fasting glucose; weight; liver enzymes; amylase/lipase
Stacks well with
Not combined with other GLP-1 agonists.
Secondary uses
T2D; liver fat reduction; visceral fat
Research status
Phase 2/3 human trials (Innovent Biologics/Eli Lilly); primarily Asia-Pacific data; GLORY Phase 3 results 2025
FDA status
No
Legal status
US: Not FDA-approved; research chemical · UK: Legal for research · Canada: Legal research chemical · Australia: Not TGA-approved · EU: Not EMA-approved
Typical price
$100–$300 / vial (limited)
Research evidence
high
Indications
Obesity and weight management (approved indication in China); Type 2 diabetes treatment (clinical trials); Metabolic syndrome research; Comparative efficacy studies vs semaglutide and tirzepatide
Chemical data
CAS 2259884-03-0 · C210H322N46O67 · 4563.1 Da
Amino acids
158 aa

Sermorelin + Ipamorelin

aka Combo, Sermorelin + Ipamorelin Clinic Combination

Moderate

How it works: Pairs two growth-hormone boosters - Sermorelin and Ipamorelin - to roughly double the GH pulse compared with either alone.

GH axis optimization via two-compound synergistic protocol; body composition; sleep; anti-aging

Research dose

200-300 mcg each, Pre-bed daily or 5 on/2 off

Real-world (reported)

Same as CJC+Ipa: 200–300 mcg each pre-bed SubQ. 5 on/2 off.

Administration

SubQ

Timing

Pre-bed 15–30 min; 2h fast preferred

Cycle length

8–16 wks on; 4–6 wks off

Real-world figures are community-reported, not medical advice.

Common side effects: Same as CJC-1295+Ipa: flushing; water retention; head rush; hunger (milder than GHRP-6)

Community take: [ANECDOTAL] Standard Rx anti-aging clinic protocol. 'What the clinic prescribed.' Community has largely switched to CJC-1295 no DAC for gray-market use (more potent and available).

Onset
GH pulse 30 min; sleep 1–2 wks; body composition 8–12 wks
Half-life
Sermorelin ~10–20 min; Ipa ~2h
Storage
Dry: Fridge 2–8°C; freeze blended vials ≤7 days · Reconstituted: Refrigerate; use within 28 days
Reconstitution
Blended vial per compounding pharmacy instructions; or reconstitute separately
Rare side effects
Same as CJC+Ipa; joint pain at high dose; glucose changes
Contraindications
Active malignancy; pregnancy; hypothyroidism (treat first)
Drug interactions
Glucocorticoids; insulin
Recommended bloodwork
IGF-1 (baseline + 4–8 wks); fasting glucose; thyroid
Stacks well with
Note: CJC-1295 no DAC has replaced Sermorelin in most community use. Sermorelin still used in Rx anti-aging clinics.
Secondary uses
Same as CJC+Ipa but using Sermorelin (shorter half-life GHRH; was FDA-approved)
Research status
Established anti-aging clinic protocol based on Sermorelin NDA data + ipamorelin preclinical/clinical experience
FDA status
No
Legal status
US: Compounding pharmacy Rx; gray-market research chemical · UK: Legal for research; Rx compounding · Canada: Legal · Australia: Schedule 4 (Rx) · EU: Varies
Typical price
$40–$80 / blended vial

Adipotide

aka CKGGRAKDC-GG-D(KLAKLAK)2, FTPP, Fat-Targeted Proapoptotic Peptide

AdvancedPhase 3

How it works: An experimental compound that cuts off the blood supply feeding fat tissue, studied for rapid targeted fat loss in animals - research only.

Highly targeted fat loss by destroying blood supply to adipose tissue (research only)

Real-world (reported)

Pure research — not recommended; primate kidney toxicity confirmed

Administration

Research only

Timing

Research only

Cycle length

Research only

Real-world figures are community-reported, not medical advice.

Common side effects: SERIOUS: Kidney toxicity (lethal at effective doses in primates); off-target apoptosis

Community take: [ANECDOTAL] NO ESTABLISHED HUMAN PROTOCOL — DO NOT SELF-ADMINISTER

Onset
Research only
Half-life
Research only
Storage
Dry: N/A — research only
Reconstitution
Freeze –20°C
Rare side effects
ALL CONTRAINDICATED — no human use
Contraindications
All renal-toxic compounds; Pre-existing renal disease or impaired kidney function; Active malignancy (theoretical concern with vascular disruption); Pregnancy and lactation (no safety data); Pediatric populations (no safety data)
Drug interactions
Renal panel mandatory if ever used — do not use
Recommended bloodwork
Do NOT use in humans
Stacks well with
[ANECDOTAL] Extreme fringe reports only. Community consensus: dangerous. Renal toxicity in primates is confirmed.
Secondary uses
Obesity research
Research status
Primate studies (Kolonin 2004 Nature Medicine); NO human trials; SEVERE renal toxicity at effective doses in primates
FDA status
No
Legal status
US: Legal for research (extreme caution required) · UK: Legal research chemical · Canada: Schedule 4; extreme risk · Australia: Unregulated; extreme risk · EU: Extremely limited; preclinical research only
Typical price
Not applicable
Research evidence
low
Indications
Obesity and metabolic syndrome research; Adipose tissue biology studies; Vascular-targeted therapeutic development
Chemical data
C105H195N33O26S2 · 2460 Da
Amino acids
224 aa

Retatrutide

aka Reta, LY3437943, ELI-002

AdvancedPhase 3

How it works: Targets three different gut hormones at once to powerfully curb appetite and raise calorie burn - studied as one of the strongest fat-loss compounds yet.

Obesity treatment; weight management; maximal fat loss

Research dose

2-12 mg, Once weekly (SubQ)

Real-world (reported)

Titration: 2 mg wk 1–4; 4 mg next 4 wks; 8 mg if tolerated. Many stop at 4–8 mg.

Administration

SubQ

Timing

Once weekly any time

Cycle length

Titration: 2 mg ×4 wk → 4 → 8 → 12 mg per tolerance

Real-world figures are community-reported, not medical advice.

Common side effects: Nausea; vomiting; diarrhea; constipation; injection-site reactions

Community take: [ANECDOTAL – r/Peptides, r/TransientMeds] Early adopters report 15–25% body weight loss over 3–6 mo. HR increase and nausea main complaints. $6.37/mg median price Q1 2026.

Onset
GI effects within days; weight loss 8+ wks
Half-life
~6 days
Storage
Dry: Fridge 2–8°C; protect from light · Reconstituted: Refrigerate; use within 28 days
Reconstitution
Verify mg/mL from vendor; typically 2 mL BAC water per vial
Rare side effects
Heart rate increase (Phase 2: mean +5–7 bpm — unique safety signal); gallstones; pancreatitis; thyroid concern (class effect)
Contraindications
MEN2/medullary thyroid history; CV disease with HR sensitivity; pregnancy; active pancreatitis; Personal or family history of medullary thyroid carcinoma (MTC) (expected class-; Multiple endocrine neoplasia syndrome type 2 (MEN2) (expected class-based contra; Pregnancy (no safety data; potential fetal risk from weight loss); Known hypersensitivity to retatrutide or any excipient (expected based on class)
Drug interactions
Insulin/antidiabetics; tachycardia-inducing drugs (HR monitoring needed)
Recommended bloodwork
Fasting glucose; HbA1c; HR and BP; lipid panel; eGFR; weight; amylase/lipase; thyroid
Stacks well with
Not combined with other GLP-1 agonists. Metformin may co-prescribe in T2D trials.
Secondary uses
T2D; NASH/NAFLD; metabolic syndrome
Research status
Phase 2 complete (NEJM 2023); Phase 3 TRIUMPH trials ongoing; no FDA approval yet
FDA status
No (Phase 3 ongoing 2026)
Legal status
US: Not FDA-approved; research chemical; not legally compounded · UK: Legal research chemical · Canada: Legal research chemical · Australia: Not TGA-approved; Schedule 4 importation risk · EU: Not EMA-approved; research chemical
Typical price
$2.77–$6.37+/mg; 10 mg vial $80–$120; 30 mg ~$200
Research evidence
low
Indications
Investigational treatment for obesity; Investigational treatment for type 2 diabetes; Under study for metabolic dysfunction-associated steatotic liver disease (MASLD)
Chemical data
CAS 2381089-83-2 · C221H342N46O68 · 4731.41 Da
Amino acids
3069 aa

Follistatin-344

aka FST-344, FST, Activin-Binding Protein

AdvancedPhase 1

How it works: Blocks myostatin (the muscle-growth limiter) like FST-315, but circulates more widely for a more systemic, whole-body effect.

Muscle hypertrophy; fat loss; anti-catabolic — more systemic than FST-315

Research dose

100-200 mcg, 2×/week

Real-world (reported)

100–200 mcg SubQ 2×/week. Monitor FSH/testosterone closely.

Administration

SubQ / IM

Timing

Post-workout

Cycle length

4–8 weeks; 4+ weeks off

Real-world figures are community-reported, not medical advice.

Common side effects: Injection-site; headache; possible excessive muscle growth; FSH suppression

Community take: [ANECDOTAL] Even more limited than FST-315 due to systemic effects and FSH impact. Advanced bodybuilding only.

Onset
Anabolic effects 2–4 wks
Half-life
Hours
Storage
Dry: Freeze –20°C · Reconstituted: Refrigerate; use within 7–14 days
Reconstitution
Add 1 mL acetic acid (0.6%) or BAC water — store advice varies
Rare side effects
Excessive hypertrophy; FSH suppression (reproductive); limited long-term safety data
Contraindications
Active malignancy; pregnancy; fertility goals (FSH/reproductive effects); Active malignancy (theoretical concern with growth factor modulation); Pre-existing antibodies to AAV1 (for gene therapy applications); Pregnancy and breastfeeding (no safety data); Severe hepatic impairmentFrequency distribution of reported side effects⚠Drug I
Drug interactions
Testosterone/sex hormones; FSH
Recommended bloodwork
IGF-1; testosterone; FSH; LH; CBC; body composition
Stacks well with
Ipamorelin + CJC-1295: muscle building stack. FST-315: local targeting alternative.
Secondary uses
Bone density; fertility modulation; fibrosis; FSH regulation
Research status
Preclinical animal data; gene therapy studies; no standalone clinical trials
FDA status
No
Legal status
US: Research use only · UK: Legal for research · Canada: Legal research chemical · Australia: Schedule 4 · EU: Unregulated
Typical price
$200–$500+ / 1 mg
Research evidence
moderate
Indications
Muscular dystrophy gene therapy research; Muscle wasting and sarcopenia studies; Metabolic disease research
Chemical data
CAS 136470-78-5 · Glycoprotein (multiple isoforms) · (approx)CharacteristicsFST-288288~31 kDa
Amino acids
344 aa

Hexarelin

aka Examorelin, EP-23905, Hexarelin Acetate

AdvancedPhase 2

How it works: The strongest growth-hormone-pulse peptide, with a separate heart-protective action - though the body adapts to it quickly with daily use.

Strongest GH pulse of any GHRP; body composition; potential cardiovascular protective effects

Research dose

100-200 mcg, 1–2×/day MAX; discontinue if no response after 4 wks

Real-world (reported)

100 mcg 1× daily or 2× max with 2+ days off between doses. Stack with Mod GRF 1-29.

Administration

SubQ / IM

Timing

Pre-workout or pre-bed

Cycle length

4–8 wks; 4–8 wks off mandatory

Real-world figures are community-reported, not medical advice.

Common side effects: Cortisol/prolactin bump; head rush; hunger; injection-site reactions

Community take: [ANECDOTAL] 'Most powerful GHRP but burns out quickly.' Used for short blast cycles. Not for long continuous use.

Onset
GH pulse 30–60 min
Half-life
~70 min
Storage
Dry: Fridge 2–8°C; freeze long-term · Reconstituted: Refrigerate; use within 28 days
Reconstitution
Add 2 mL BAC water to 2 mg vial = 1 mg/mL; 100 mcg = 10 IU
Rare side effects
Rapid and significant receptor desensitization (tachyphylaxis) with >2× daily dosing; cortisol elevation
Contraindications
Active malignancy; pregnancy; prolactin-sensitive conditions; frequent dosing (causes desensitization); Active cancer or history of malignancy (GH and IGF-1 elevation may promote tumor; Pituitary tumors or pituitary disorders (risk of exacerbating underlying conditi; Pregnancy and breastfeeding (no reproductive safety data available)Frequency dis; Growth hormone and IGF-1 axis drugs (potential additive GH elevation and IGF-1 i
Drug interactions
Glucocorticoids; prolactin-modulating drugs
Recommended bloodwork
IGF-1; cortisol; prolactin; GH levels optional; monitor desensitization via GH response
Stacks well with
CJC-1295 no DAC: pair only if avoiding desensitization schedule. Most experienced users prefer ipamorelin for long cycles.
Secondary uses
IGF-1 elevation; cardioprotective (independent of GH); healing
Research status
Preclinical robust; some human Phase 2 data; cardioprotective effects studied
FDA status
No
Legal status
US: Research use only · UK: Legal for research · Canada: Legal research chemical · Australia: Schedule 4 · EU: Unregulated
Typical price
$25–$55 / 2 mg vial
Research evidence
moderate
Indications
Growth hormone deficiency research; Cardiovascular protection studies; Neuroendocrine research; Anti-aging investigations
Chemical data
CAS 140703-51-1 · C47H58N12O6 · 887 Da
Amino acids
240 aa

Cagrilintide

aka AM833, OIC-02, NN9838

AdvancedPhase 3

How it works: Curbs appetite through the amylin system - a different pathway than GLP-1 drugs - which is why it is often combined with semaglutide for stronger weight loss.

Weight loss (combination with semaglutide in CagriSema); satiety; glycemic control

Research dose

0.16-4.5 mg, Once weekly (SubQ)

Real-world (reported)

Very limited community protocols — follow Phase 3 titration as guide.

Administration

SubQ

Timing

Once weekly any time

Cycle length

Chronic; titration per protocol

Real-world figures are community-reported, not medical advice.

Common side effects: Nausea; vomiting; injection-site reactions; constipation

Community take: [ANECDOTAL] Limited community experience standalone. Combined CagriSema reports: superior weight loss vs either alone. Main issue: additive GI side effects.

Onset
GI effects within days; weight loss 8+ wks
Half-life
~7–8 days
Storage
Dry: Fridge 2–8°C; protect from light · Reconstituted: Refrigerate; use within 28 days
Reconstitution
Verify mg/mL from vendor
Rare side effects
Pancreatitis; gallstones; amylin receptor effects; HR changes
Contraindications
Active pancreatitis; pregnancy; MEN2 history (combination semaglutide carries black box); Personal or family history of medullary thyroid carcinoma (applies to CagriSema; Multiple endocrine neoplasia syndrome type 2 (MEN2; applies to CagriSema combina; History of pancreatitis; Pregnancy and breastfeeding (no reproductive safety data)
Drug interactions
Insulin; semaglutide combination (monitor GI side effects closely in combination)
Recommended bloodwork
Fasting glucose; HbA1c; weight; GI symptom monitoring; amylase/lipase
Stacks well with
Semaglutide: Phase 3 CagriSema combination (additive weight loss).
Secondary uses
Standalone metabolic benefits; potential for NASH; reduced CV risk
Research status
Phase 3 REDEFINE trials (CagriSema combination ongoing 2025–2026); Phase 2 data published
FDA status
No (Phase 3)
Legal status
US: Not FDA-approved; research chemical · UK: Legal for research · Canada: Legal research chemical · Australia: Not TGA-approved; Schedule 4 risk · EU: Not EMA-approved; research chemical
Typical price
$100–$300 / vial (limited supply)
Research evidence
moderate
Indications
Obesity treatment; Weight management; Metabolic disease research
Chemical data
CAS 2170438-03-2 · C194H312N54O59S2 · 4030 Da
Amino acids
127 aa

Follistatin-315

aka FST-315

Advanced

How it works: Blocks myostatin, the protein that limits muscle growth, releasing the brake on muscle - this version acts more on local tissues.

Muscle hypertrophy; fat loss; anti-catabolic; potential anti-aging via muscle preservation

Research dose

100-200 mcg, Twice weekly

Real-world (reported)

100 mcg SubQ 2×/week. Advanced users only. Monitor FSH/testosterone.

Administration

SubQ / IM

Timing

Post-workout

Cycle length

4–8 weeks; 4+ weeks off

Real-world figures are community-reported, not medical advice.

Common side effects: Injection-site reactions; headache; possible excessive muscle growth

Community take: [ANECDOTAL – advanced bodybuilding] 'Extreme muscle growth.' Limited community experience due to difficulty sourcing and high cost. Reported results impressive but safety profile uncertain.

Onset
Muscle anabolic effects 2–4 wks
Half-life
Hours (clearance)
Storage
Dry: Freeze –20°C · Reconstituted: Refrigerate; use within 7–14 days
Reconstitution
Add 1 mL ACetic acid (0.6%) or BAC water
Rare side effects
Excessive muscle hypertrophy; limited long-term safety data; theoretical concern re activin in reproductive axis; testosterone suppression (activin inhibition affects FSH)
Contraindications
Active malignancy; pregnancy; desire for future fertility (FSH/reproductive effects); hormone-sensitive conditions
Drug interactions
Testosterone/sex hormones (activin pathway); FSH (reproductive monitoring needed)
Recommended bloodwork
IGF-1; testosterone; FSH; LH; CBC; body composition
Stacks well with
Ipamorelin + CJC-1295: muscle building stack. IGF-1 LR3: advanced anabolic stack.
Secondary uses
Bone density; fertility modulation; fibrosis reduction
Research status
Preclinical animal data robust; gene therapy studies; limited human pharmacology; no clinical trials as standalone
FDA status
No
Legal status
US: Research use only · UK: Legal for research · Canada: Legal research chemical · Australia: Schedule 4 · EU: Unregulated
Typical price
$200–$500+ / 1 mg vial

AICAR

aka Acadesine, Acadesine, AICA-riboside

Advanced

How it works: Switches on AMPK, the same cellular energy pathway exercise activates, to mimic endurance-training effects like fat burning.

Metabolic conditioning; fat oxidation; endurance enhancement; AMPK activation

Research dose

250-500 mg, Daily

Real-world (reported)

250–500 mg oral or SubQ daily. Pre-workout. Cycle 4–8 wks.

Administration

Oral / SubQ

Timing

Pre-workout or morning

Cycle length

4–8 wks; WADA prohibited in competition

Real-world figures are community-reported, not medical advice.

Common side effects: Nausea; headache; hypoglycemia (mild); malaise at high doses

Community take: [ANECDOTAL] WADA prohibits it — signals effectiveness. Limited gray-market but present.

Onset
Metabolic changes 2–4 wks
Half-life
~2–3h
Storage
Dry: Room temp (oral); fridge (injectable) · Reconstituted: Injectable: refrigerate; use within 7 days
Reconstitution
Oral: no recon. Injectable: dissolve in sterile water.
Rare side effects
Mitochondrial enzyme inhibition (supraphysiologic; theoretical); WADA prohibited
Contraindications
Competitive athletes (WADA banned); malignancy (AMPK complex in cancer); pregnancy
Drug interactions
Metformin (additive AMPK); insulin
Recommended bloodwork
Fasting glucose; HbA1c; lipid panel
Stacks well with
MOTS-c: additive AMPK. 5-Amino-1MQ: metabolic stack.
Secondary uses
Insulin sensitivity; anti-cancer (AMPK); cardiovascular protection
Research status
Preclinical robust; Phase 2 cardiac surgery and multiple myeloma; WADA prohibited for sport
FDA status
No
Legal status
US: Research use only; WADA anti-doping prohibited · UK: Legal for research; WADA prohibited in sport · Canada: Legal research chemical · Australia: Schedule 4 · EU: Unregulated for research
Typical price
$30–$80 / 500 mg

Irisin

aka FNDC5 ectodomain, exercise myokine

Advanced

How it works: The exercise hormone your muscles release during workouts, which turns calorie-storing white fat into calorie-burning fat and supports brain health.

White fat browning; thermogenesis; metabolic rate; cognitive enhancement; anti-aging

Research dose

500-1000 mcg, 3×/week

Real-world (reported)

500 mcg SubQ 3×/week — very experimental.

Administration

SubQ

Timing

Any time or pre-workout

Cycle length

8–12 weeks

Real-world figures are community-reported, not medical advice.

Common side effects: Very limited: injection-site; mild metabolic changes

Community take: [ANECDOTAL] 'Exercise hormone injection.' Phase 1 limited. Mostly preclinical interest. Very small biohacker community.

Onset
Metabolic 4–8 wks; cognitive 2–4 wks
Half-life
~2–4h estimated
Storage
Dry: Freeze –20°C; light sensitive · Reconstituted: Refrigerate; use within 14 days
Reconstitution
Add 1 mL BAC water to 1 mg vial
Rare side effects
No human trial safety data; cancer context complex (FNDC5 in some tumors)
Contraindications
Active malignancy (complex); pregnancy
Drug interactions
Insulin/metabolic drugs
Recommended bloodwork
Fasting glucose; body composition; BDNF; lipid panel
Stacks well with
MOTS-c: exercise mimetic synergy. AICAR: AMPK complement.
Secondary uses
Bone formation; insulin sensitivity; neuroprotection; exercise mimicry
Research status
Preclinical extensive (Boström 2012 Nature landmark); human correlation studies; limited Phase 1 PK
FDA status
No
Legal status
US: Research use only · UK: Legal for research · Canada: Legal research chemical · Australia: Schedule 4 · EU: Unregulated
Typical price
$100–$400 / 1 mg vial

CJC-1295 + GHRP-6

aka Bulk Stack, CJC-1295 no DAC + GHRP-6 combination

Advanced

How it works: A bulking stack of two growth-hormone boosters for a strong GH pulse, with GHRP-6 also driving big appetite to support eating in a surplus.

Maximum GH pulse for bulking; muscle mass; strong appetite stimulation — useful for hard gainers

Research dose

200-300 mcg each, Pre-bed; or pre-workout for bulking push

Real-world (reported)

200–300 mcg each SubQ 1–2×/day. ONLY for bulking — prepare food before injecting GHRP-6.

Administration

SubQ

Timing

Pre-bed or pre-workout; 2h fast before

Cycle length

8–12 wks on; 4 wks off

Real-world figures are community-reported, not medical advice.

Common side effects: Strong hunger/appetite (GHRP-6 signature); head rush; flushing; cortisol bump; water retention

Community take: [ANECDOTAL] Old-school bulking GH stack. GHRP-6 hunger is intense. 'Eat everything in the house after injecting.' Replaced by CJC+Ipa for most uses except hard-gainer bulk phases.

Onset
GH pulse 30 min; strong hunger within minutes; body composition 8–12 wks
Half-life
CJC: ~30 min; GHRP-6: ~30 min
Storage
Dry: Fridge 2–8°C; freeze long storage · Reconstituted: Refrigerate; use within 28 days
Reconstitution
Reconstitute each separately; inject simultaneously or sequentially
Rare side effects
Cortisol elevation; prolactin elevation (GHRP-6); significant appetite may cause unwanted weight gain if not in bulk phase
Contraindications
Cutting/fat-loss goals (appetite stimulus); active malignancy; pregnancy
Drug interactions
Glucocorticoids; prolactin-modulating drugs
Recommended bloodwork
IGF-1; cortisol; prolactin; body weight; fasting glucose
Stacks well with
Note: for non-bulk goals, replace GHRP-6 with Ipamorelin (no appetite/cortisol issues).
Secondary uses
Body recomposition (if appetite managed); recovery
Research status
Community protocol based on established CJC-1295 + GHRP-6 pairing literature
FDA status
No
Legal status
US: Research use only · UK: Legal for research · Canada: Legal research chemical · Australia: Schedule 4 · EU: Unregulated
Typical price
$35–$75 combined per dose session

Amycretin

aka NNC0487-0111

ModeratePhase 1b

How it works: Amycretin (NNC0487-0111) is a first-in-class unimolecular GLP-1 and amylin receptor agonist developed by Novo Nordisk. Unlike CagriSema (two separate peptides), amycretin combines both activities in a single 68-amino-acid molecule. In Phase 1b/2a, subcutaneous amycretin achieved up to 24.3% weight loss at 36 weeks (60 mg) and 22% at 20 mg. Oral amycretin achieved up to 13.1% at 12 weeks. Phase 3 f

Chronic weight management in adults with obesity or overweight; Type 2 diabetes treatment

Administration

SC

Timing

Dose escalation required. SC formulation administered weekly; oral formulation with SNAC enhancer taken daily. Both formulations under investigation.

Cycle length

Up to 36 weeks (Phase 1b/2a)

Half-life
Supports once-weekly SC dosing and once-daily oral dosing via albumin binding fr
Contraindications
Amycretin is investigational and not approved for any indication. Use only withi; Expected GLP-1 agonist class contraindication: personal or family history of med; Pregnancy (GLP-1 agonist class); Prior serious hypersensitivity to amycretin or excipientsFrequency distribution
Research status
Phase 1b
Legal status
US: Investigational
Research evidence
moderate
Indications
Chronic weight management in adults with obesity or overweight; Type 2 diabetes treatment
Chemical data
C343H550N94O116 · 8000 Da
Amino acids
127 aa

Insulin

aka Human Insulin, Regular Insulin, Humulin

ModerateApproved

How it works: Insulin is a 51-amino acid peptide hormone produced by pancreatic beta cells, consisting of an A-chain (21 amino acids) and B-chain (30 amino acids) linked by disulfide bonds. It is the primary regulator of blood glucose homeostasis and has been used therapeutically since 1922 for diabetes management.New to metabolic peptides?Browse all metabolic peptides →Table of Contents📌TL;DR•Essential hormon

Type 1 diabetes mellitus management; Type 2 diabetes mellitus (when oral agents insufficient); Diabetic ketoacidosis emergency treatment; Hyperkalemia management in acute care settings

Administration

SC

Timing

Rapid-acting: 15 min before meals or pre/post-workout with carbohydrates✓ Rotate injection sites

Cycle length

Diabetes: chronic therapy; Off-label: cycles of 4-8 weeks

Half-life
~6 minutes (IV); ~6-8 hours clinical duration (SC regular insulin); ~
Contraindications
Hypersensitivity to insulin or any formulation component; During active hypoglycemic episodes; Inhaled insulin: contraindicated in chronic lung disease (asthma, COPD) due to b; Sulfonylureas, meglitinides, DPP-4 inhibitors, GLP-1 RAs: increased hypoglycemia
Research status
Approved
FDA status
FDA approved
Legal status
US: Approved
Research evidence
high
Indications
Type 1 diabetes mellitus management; Type 2 diabetes mellitus (when oral agents insufficient); Diabetic ketoacidosis emergency treatment; Hyperkalemia management in acute care settings
Chemical data
CAS 11061-68-0 · C257H383N65O77S6 · 5808 Da
Amino acids
123 aa

Bioglutide

aka NA-931, NA-931

ModeratePhase 2

How it works: Bioglutide (NA-931) is a first-in-class, orally active small-molecule quadruple receptor agonist developed by Biomed Industries that simultaneously targets IGF-1, GLP-1, GIP, and glucagon receptors. Derived from a cyclic IGF-1 fragment, it is designed as a once-daily oral capsule requiring no absorption enhancers. In Phase 2 trials (NCT06564753), the 150 mg daily dose achieved 13.8% mean body weig

Chronic weight management in adults with obesity (BMI 30 or greater); Weight management in overweight adults (BMI 27 or greater) with weight-related comorbidities; Potential combination therapy with tirzepatide for enhanced efficacy

Administration

Oral

Timing

Take one capsule once daily by mouth. No fasting or food restrictions required. Blood levels consistent regardless of fasting state or high-fat meal.

Cycle length

13 weeks (Phase 2 trial)

Half-life
Estimated 16-
Contraindications
Hypersensitivity to NA-931 or any component of the formulation (based on standar; Pregnancy and breastfeeding (no reproductive toxicology data available; standard; No drug interaction data have been published for Bioglutide (NA-931). Potential
Research status
Phase 2
FDA status
Not approved
Legal status
US: Investigational
Research evidence
low
Indications
Chronic weight management in adults with obesity (BMI 30 or greater); Weight management in overweight adults (BMI 27 or greater) with weight-related comorbidities; Potential combination therapy with tirzepatide for enhanced efficacy
Chemical data
Proprietary (not publicly disclosed) · 500 Da
Amino acids
74 aa

MariTide

aka maridebart cafraglutide, AMG 133

ModeratePhase 2

How it works: MariTide (maridebart cafraglutide, AMG 133) is a first-in-class antibody-peptide conjugate developed by Amgen that combines GLP-1 receptor agonism with GIP receptor antagonism. Unlike tirzepatide (GLP-1/GIP dual agonist), MariTide blocks the GIP receptor while activating GLP-1. Its ~21-day half-life enables monthly or less frequent dosing. In Phase 2, MariTide achieved up to 16.2% weight loss at 5

Chronic weight management in adults with obesity or overweight; Type 2 diabetes treatment

Administration

SC

Timing

Delivered via autoinjector device. Half-life of approximately 21 days supports monthly dosing. Dose escalation likely used per GLP-1 class standard.

Cycle length

52 weeks (Phase 2); 72 weeks (Phase 3)

Half-life
, and pharmacokinetic properties.","url":"https://www.peptideprotocolwiki.com/pe
Contraindications
MariTide is investigational and not approved for any indication. Use only within; Expected GLP-1 agonist class contraindication: personal or family history of med; Pregnancy (GLP-1 agonist class); Prior serious hypersensitivity to MariTide or excipientsFrequency distribution o
Research status
Phase 2
FDA status
Not approved
Legal status
US: Investigational
Research evidence
moderate
Indications
Chronic weight management in adults with obesity or overweight; Type 2 diabetes treatment
Chemical data
Complex antibody-peptide conjugate · 153514 Da
Amino acids
114 aa

CagriSema

aka Cagrilintide/Semaglutide, NNC0174-0833

ModeratePhase 3

How it works: CagriSema is a once-weekly fixed-dose combination of cagrilintide 2.4 mg (a long-acting amylin receptor agonist) and semaglutide 2.4 mg (a GLP-1 receptor agonist), developed by Novo Nordisk. In the Phase 3 REDEFINE 1 trial, CagriSema achieved 20.4% mean weight loss at 68 weeks in adults with obesity, exceeding semaglutide alone (14.9%) and cagrilintide alone (11.5%). Novo Nordisk has filed for FDA

Chronic weight management in adults with obesity or overweight; Type 2 diabetes with obesity (REDEFINE 2); Cardiometabolic risk factor improvement

Administration

SC

Timing

Single injection from pre-filled pen combining both agents. Gradual dose escalation over 16-20 weeks to reach target maintenance dose. Inject on the s

Cycle length

68 weeks (Phase 3 trials)

Half-life
Cagrilintide: ~160 hours (6.7 days); Semaglutide: ~168 hours (7 days)
Contraindications
Personal or family history of medullary thyroid carcinoma (MTC) or Multiple Endo; Pregnancy (semaglutide component); Prior serious hypersensitivity to cagrilintide, semaglutide, or excipientsFreque; Insulin and sulfonylureas: Increased risk of hypoglycemia when combined (GLP-1 a
Research status
Phase 3
FDA status
Not approved
Legal status
US: Investigational
Research evidence
high
Indications
Chronic weight management in adults with obesity or overweight; Type 2 diabetes with obesity (REDEFINE 2); Cardiometabolic risk factor improvement
Chemical data
Combination product (cagrilintide C188H289N51O57S2 + semaglutide C187H291N45O59) · 8144 Da
Amino acids
170 aa

CT-388

aka RO7795068

ModeratePhase 2

How it works: CT-388 is a signal-biased dual GLP-1/GIP receptor agonist developed by Roche (acquired via Carmot Therapeutics). Its unique biased signaling minimizes beta-arrestin recruitment and receptor internalization at both receptors. In Phase 2, weekly subcutaneous CT-388 (24 mg) achieved 22.5% placebo-adjusted weight loss at 48 weeks with no plateau observed. Phase 3 trials are planned for 2026.New to met

Chronic weight management in adults with obesity or overweight; Potential for type 2 diabetes treatment; Potential for metabolic dysfunction-associated steatohepatitis (MASH)

Administration

SC

Timing

Dose escalation from lower starting dose to maintenance dose to mitigate GI adverse events. Same day each week.

Cycle length

48 weeks (Phase 2)

Half-life
Supports once-weekly subcutaneous dosing (exact half-life not publicly disclosed
Contraindications
CT-388 is investigational and not approved for any indication. Use only within c; Expected GLP-1 agonist class contraindication: personal or family history of med; Pregnancy (GLP-1 agonist class); Prior serious hypersensitivity to CT-388 or excipientsFrequency distribution of
Research status
Phase 2
FDA status
Not approved
Legal status
US: Investigational
Research evidence
moderate
Indications
Chronic weight management in adults with obesity or overweight; Potential for type 2 diabetes treatment; Potential for metabolic dysfunction-associated steatohepatitis (MASH)
Chemical data
Proprietary (not disclosed) · 4500 Da
Amino acids
101 aa

Pramlintide

aka Symlin, Symlin, AC137

ModerateApproved

How it works: Pramlintide (marketed as Symlin) is a synthetic analog of human amylin, a 37-amino acid peptide hormone co-secreted with insulin from pancreatic beta cells. FDA-approved in March 2005 as an adjunct to mealtime insulin in patients with type 1 or type 2 diabetes who have not achieved adequate glycemic control. Pramlintide contains three proline substitutions (Pro25,28,29) that prevent the amyloid ag

Adjunct to mealtime insulin in type 1 diabetes (FDA-approved 2005); Adjunct to mealtime insulin in type 2 diabetes (FDA-approved 2005)

Administration

SC

Timing

Inject immediately before major meals containing 250+ calories or 30g carbohydrate. Never mix with insulin in the same syringe.

Cycle length

Ongoing

Half-life
.","url":"https://www.peptideprotocolwiki.com/peptides/pramlintide/molecule","da
Contraindications
Confirmed diagnosis of gastroparesis requiring treatment; Hypoglycemia unawareness (increased risk of severe hypoglycemia); HbA1c >9% (poor glycemic control suggests need for basic insulin optimization be; Recurrent episodes of severe hypoglycemia in the past 6 months
Research status
Approved
FDA status
FDA approved
Legal status
US: Approved
Research evidence
high
Indications
Adjunct to mealtime insulin in type 1 diabetes (FDA-approved 2005); Adjunct to mealtime insulin in type 2 diabetes (FDA-approved 2005)
Chemical data
CAS 151126-32-8 · C171H267N51O53S2 · 3949.4 Da
Amino acids
37 aa

Exenatide

aka Byetta, Bydureon, exendin-4

ModerateApproved

How it works: Exenatide is a 39-amino-acid synthetic version of exendin-4, a peptide originally discovered in Gila monster (Heloderma suspectum) venom. It was the first GLP-1 receptor agonist approved by the FDA (Byetta, April 2005), establishing the entire incretin mimetic drug class. Available as Byetta (twice-daily injection) and Bydureon BCise (once-weekly extended-release microsphere formulation), exenatid

Type 2 diabetes glycemic control (adjunct to diet and exercise); Investigational: Parkinson's disease neuroprotection

Administration

SC

Timing

Byetta: within 60 minutes before meals; Bydureon BCise: any time, any day✓ Rotate injection sites

Cycle length

Ongoing (chronic therapy)Step-wise Titration (4 weeks)

Half-life
. Glycine at position
Storage
Dry: Byetta: refrigerate or room temp up to 30 days after first use. Bydureon BCise: refrigerate or room temp up to 4 weeks.
Contraindications
Personal or family history of medullary thyroid carcinoma (MTC) or Multiple Endo; Prior serious hypersensitivity reaction to exenatide or any excipient; Severe renal impairment (eGFR below 30 mL/min) or end-stage renal disease (exena; Do not use with other GLP-1 receptor agonists (e.g., semaglutide, liraglutide, t
Research status
Approved
FDA status
FDA approved
Legal status
US: Approved
Research evidence
high
Indications
Type 2 diabetes glycemic control (adjunct to diet and exercise); Investigational: Parkinson's disease neuroprotection
Chemical data
CAS 141758-74-9 · C184H282N50O60S · 4186.6 Da
Amino acids
4 aa

Pemvidutide

aka ALT-801

ModeratePhase 2b

How it works: Pemvidutide (ALT-801) is a 29-amino acid dual GLP-1/glucagon receptor agonist developed by Altimmune for obesity and metabolic dysfunction-associated steatohepatitis (MASH). In Phase 2b trials, it achieved 59.1% MASH resolution, 54.7% liver fat reduction, and 15.6% weight loss at 48 weeks. Its unique dual mechanism addresses both weight and liver disease simultaneously.New to metabolic peptides?Br

Obesity and overweight with comorbidities; Metabolic dysfunction-associated steatohepatitis (MASH); Metabolic dysfunction-associated steatotic liver disease (MASLD)

Administration

SC

Timing

No dose titration required; patients start directly on target dose unlike most GLP-1 agonists

Cycle length

48 weeks (Phase 2b)

Half-life
Approximately 100 hours (supports once-weekly dosing)
Contraindications
Investigational compound: not approved for clinical use; Expected class contraindications based on GLP-1 receptor agonist class including; Drug interactions not fully characterized. GLP-1 component may delay gastric emp
Research status
Phase 2b
Legal status
US: Investigational
Research evidence
moderate
Indications
Obesity and overweight with comorbidities; Metabolic dysfunction-associated steatohepatitis (MASH); Metabolic dysfunction-associated steatotic liver disease (MASLD)
Chemical data
Proprietary (not publicly disclosed) · 3873.35 Da
Amino acids
68 aa

Setmelanotide

aka IMCIVREE, IMCIVREE, RM-493, BMS-470539

ModerateApproved

How it works: Setmelanotide (marketed as IMCIVREE) is a first-in-class melanocortin-4 receptor (MC4R) agonist developed by Rhythm Pharmaceuticals. FDA-approved in November 2020 for chronic weight management in patients aged 6 years and older with obesity due to POMC, PCSK1, or LEPR deficiency confirmed by genetic testing. This cyclic 8-amino acid peptide (1.1 kDa) represents the first targeted therapy for monog

Chronic weight management in POMC deficiency obesity (FDA-approved 2020); Chronic weight management in PCSK1 deficiency obesity (FDA-approved 2020); Chronic weight management in LEPR deficiency obesity (FDA-approved 2020); Chronic weight management in Bardet-Biedl syndrome (FDA-approved 2022)

Administration

SC

Timing

Administer once daily at the start of the day. Inject into the abdomen. Rotate injection sites with each injection.

Cycle length

Ongoing (with 12-16 week response assessment)

Half-life
~11 hours, supporting once-daily subcutaneous injection
Contraindications
Not for use in patients without confirmed genetic variants in POMC, PCSK1, LEPR,; Not recommended during pregnancy; weight loss is not beneficial during pregnancy; Hypersensitivity to setmelanotide or any component of the formulationFrequency d; No formal drug interaction studies have been conducted due to the rare disease p
Research status
Approved
FDA status
FDA approved
Legal status
US: Approved
Research evidence
high
Indications
Chronic weight management in POMC deficiency obesity (FDA-approved 2020); Chronic weight management in PCSK1 deficiency obesity (FDA-approved 2020); Chronic weight management in LEPR deficiency obesity (FDA-approved 2020); Chronic weight management in Bardet-Biedl syndrome (FDA-approved 2022)
Chemical data
CAS 920014-72-8 · C49H68N18O9S2 · 1117.31 Da
Amino acids
248 aa

VK2735

aka VK-2735

ModeratePhase 2

How it works: VK2735 is a dual GLP-1/GIP receptor agonist peptide developed by Viking Therapeutics for obesity treatment. In the Phase 2 VENTURE trial, weekly subcutaneous VK2735 achieved up to 14.7% weight loss in just 13 weeks with no plateau observed. An oral tablet formulation achieved up to 12.2% weight loss in 13 weeks. Phase 3 VANQUISH trials are underway with enrollment of over 4,500 patients completed.

Chronic weight management in adults with obesity or overweight; Potential for type 2 diabetes treatment

Administration

SC

Timing

Dose escalation used to mitigate GI adverse events. Oral formulation does not require strict fasting conditions unlike oral semaglutide.

Cycle length

13 weeks (Phase 2); longer in Phase 3

Half-life
Supports once-weekly subcutaneous dosing (exact half-life not publicly disclosed
Contraindications
VK2735 is investigational and not approved for any indication. Use only within c; Expected GLP-1 agonist class contraindication: personal or family history of med; Pregnancy (GLP-1 agonist class); Prior serious hypersensitivity to VK2735 or excipientsFrequency distribution of
Research status
Phase 2
FDA status
Not approved
Legal status
US: Investigational
Research evidence
moderate
Indications
Chronic weight management in adults with obesity or overweight; Potential for type 2 diabetes treatment
Chemical data
Proprietary (not disclosed) · 4700 Da
Amino acids
91 aa

Neuropeptide Y

aka NPY

ModerateApproved

How it works: Neuropeptide Y (NPY) is a 36-amino acid endogenous peptide and one of the most abundant neuropeptides in the brain. It acts through Y1, Y2, Y4, and Y5 receptor subtypes to regulate appetite, anxiety, stress response, and circadian rhythms. Reduced NPY levels are associated with PTSD and depression. Intranasal NPY delivery has been tested in early clinical trials for major depression, showing preli

PTSD and stress resilience research; Depression treatment research; Appetite and energy homeostasis studies; Anxiety and mood regulation research

Administration

Intranasal

Timing

Delivered via nasal atomizer device; intranasal route bypasses blood-brain barrier for direct CNS delivery

Cycle length

Single administration

Half-life
~15-
Contraindications
Not approved for human use by any regulatory agency; Caution in individuals with cardiovascular disease (NPY causes vasoconstriction; Caution in individuals with eating disorders or obesity (NPY stimulates appetite; Potential interaction with antihypertensive medications (NPY causes vasoconstric
Research status
Approved
FDA status
FDA approved
Legal status
US: Investigational
Research evidence
moderate
Indications
PTSD and stress resilience research; Depression treatment research; Appetite and energy homeostasis studies; Anxiety and mood regulation research
Chemical data
CAS 82785-45-3 · C190H287N55O57 · 4253.72 Da
Amino acids
240 aa

HGH 191AA

aka Somatotropin, Recombinant Human Growth Hormone, rhGH

ModerateApproved

How it works: HGH 191AA is recombinant human growth hormone, a 191-amino acid single-chain polypeptide identical to endogenous pituitary-derived somatotropin. It is FDA-approved for growth hormone deficiency, Turner syndrome, chronic renal insufficiency, and other conditions affecting growth and metabolism.New to growth hormone peptides?Browse all growth hormone peptides →Table of Contents📌TL;DR•FDA-approved f

Growth hormone deficiency treatment (pediatric and adult); Turner syndrome growth support; Chronic renal insufficiency-related growth failure; AIDS-related wasting syndrome

Administration

SC

Timing

Anti-aging: before bed (mimics natural GH pulse); Performance: morning fasted and/or post-workout; avoid close to meals high in carbs/fat✓ Rotate inje

Cycle length

3-6 months minimum; some protocols run 6-12 months or longerStep-wise Titration

Half-life
SC:
Reconstitution
Bacteriostatic water
Contraindications
Acute critical illness (cardiac/abdominal surgery, multiple trauma, acute respir; Active malignancy or evidence of neoplastic activity; Active proliferative or severe non-proliferative diabetic retinopathy; Prader-Willi syndrome with severe obesity or respiratory impairment
Research status
Approved
FDA status
FDA approved
Legal status
US: Approved
Research evidence
low
Indications
Growth hormone deficiency treatment (pediatric and adult); Turner syndrome growth support; Chronic renal insufficiency-related growth failure; AIDS-related wasting syndrome
Chemical data
CAS 12629-01-5 · C990H1529N263O299S7 · 22124 Da
Amino acids
191 aa

Cotadutide

aka MEDI0382, MEDI0382, AZD9056

ModeratePhase 2b

How it works: Cotadutide (MEDI0382) was a dual GLP-1 and glucagon receptor agonist developed by AstraZeneca for type 2 diabetes, obesity, and non-alcoholic steatohepatitis (NASH). The 31-amino acid peptide with N-terminal palmitic acid conjugation demonstrated GLP-1-biased dual agonism (EC50 6.9 pM GLP-1R, 10.2 pM GCGR), producing significant improvements in glycemic control, weight loss, and hepatic parameters

Type 2 diabetes mellitus (phase 2b, discontinued); Non-alcoholic steatohepatitis / NASH (phase 2, discontinued); Obesity / weight management (phase 2, discontinued)

Administration

SC

Timing

Dose escalation from starting dose to target maintenance dose to mitigate GI adverse events. Consistent with standard GLP-1 agonist titration.

Cycle length

54 weeks (Phase 2b trial)

Half-life
~11-1
Contraindications
Development was discontinued; not available for clinical use; History of medullary thyroid carcinoma or MEN2 (GLP-1 agonist class contraindica; Known hypersensitivity to GLP-1 receptor agonistsFrequency distribution of repor; Insulin and sulfonylureas: Potential for increased hypoglycemia risk (GLP-1 agon
Research status
Phase 2b
Legal status
US: Withdrawn From Market
Research evidence
moderate
Indications
Type 2 diabetes mellitus (phase 2b, discontinued); Non-alcoholic steatohepatitis / NASH (phase 2, discontinued); Obesity / weight management (phase 2, discontinued)
Chemical data
CAS 1686108-82-6 · C169H256N42O57 (acetate salt) · 3788.14 Da
Amino acids
31 aa

TLQP-21

aka VGF-derived peptide; 21 amino acids derived from VGF precursor, VGF-derived peptide, C-terminal VGF peptide

Moderate

How it works: TLQP-21 targets the complement-3a receptor1 (C3aR1) to regulate metabolism and immune function.

Obesity management; lipolysis; energy expenditure; microglial modulation; neuroprotection; pain modulation

Research dose

2-32 nmol, Research dosing varies; chronic dosing studied via osmotic pump and daily injections

Administration

Intracerebroventricular injection (i.c.v.); intravenous (i.v.); intraperitoneal (i.p.)

Common side effects: Thermal hyperalgesia (when applied spinally)

Onset
Acute effects measurable within hours; chronic effects over weeks to 28 days
Half-life
Terminal half-life of ~110 min with an initial half-life of ~0.97 min
Rare side effects
Application of exogenous TLQP-21 induced dose-dependent thermal hyperalgesia, which was inhibited by p38 MAPK inhibitors and COX/lipoxygenase inhibitors
Secondary uses
Alzheimer's disease progression; gastric motility regulation; reproduction
Research status
Preclinical and investigational

Ecnoglutide

aka XW003, XW-003

ModeratePhase 3

How it works: Ecnoglutide (XW003) is a novel, long-acting, cAMP signaling-biased GLP-1 receptor agonist developed by Sciwind Biosciences. Unlike conventional GLP-1 agonists, ecnoglutide preferentially activates G protein-cAMP signaling over beta-arrestin recruitment, which may improve efficacy while reducing receptor desensitization. In the Phase 3 SLIMMER trial, ecnoglutide achieved 15.4% mean weight loss at 4

Chronic weight management in adults with obesity or overweight; Type 2 diabetes glycemic control

Administration

SC

Timing

Administered on the same day each week. Dose escalation from starting dose to maintenance dose to improve GI tolerability. Half-life of 124-138 hours

Cycle length

48 weeks (SLIMMER Phase 3)

Half-life
Approximately 1
Contraindications
Investigational compound: ecnoglutide is not approved for clinical use and shoul; Expected contraindications based on GLP-1 receptor agonist class: personal or fa; Pregnancy and breastfeeding (expected contraindication based on class)Frequency; Insulin and sulfonylureas: based on GLP-1 agonist class effects,
Research status
Phase 3
FDA status
Not approved
Legal status
US: Investigational
Research evidence
moderate
Indications
Chronic weight management in adults with obesity or overweight; Type 2 diabetes glycemic control
Chemical data
CAS 2459531-73-6 · C194H304N48O61 · 4256.74 Da
Amino acids
2668 aa

Alpha-Melanocyte-Stimulating Hormone

aka ACTH 1-13 fragment, α-MSH, MSH, Melanocyte-Stimulating Hormone

Moderate

How it works: Alpha-MSH is a 13-amino-acid endogenous neuropeptide derived from proopiomelanocortin (POMC), acting as a non-selective agonist at melanocortin receptors, playing central roles in pigmentation, appetite regulation, anti-inflammatory signaling, neuroprotection, and immune modulation.

Appetite suppression, anti-inflammatory signaling, immune modulation, neuroprotection

Research dose

1-100 mcg, [ANECDOTAL]—research studies used varied frequencies; intranasal single dose studies; oral ingestion in animal models; intraperitoneal injection in mouse models

Administration

Subcutaneous injection, intranasal, oral ingestion (research models), topical (eye drops), intravenous

Common side effects: Skin hyperpigmentation, darkening of preexisting nevi and ephelides, and development of melanocytic nevi are known potential side effects

Rare side effects
At doses ≥1 mg (central administration in animal models): increased salivation, agitation, ataxia, respiratory distress, and death (in 30% of animals)
Secondary uses
Fever reduction, ischemia/reperfusion injury protection, rheumatoid arthritis, inflammatory bowel disease, contact dermatitis, dry eye disease
Research status
Preclinical and animal model research; synthetic analogs in clinical trials
Legal status
US: Despite a ban by the United States Food and Drug Administration, commercially produced, unregulated peptide analogs of α-MSH (eg, melanotan, melanotan II) remain available for sale online

Efocipegtrutide

aka HM15211, HM15211, LAPS Triple Agonist

Moderate

How it works: Efocipegtrutide is a long-acting glucagon, GIP and GLP-1 triple full agonist conjugated with human immunoglobulin constant region.

MASH (metabolic dysfunction-associated steatohepatitis), obesity, non-alcoholic fatty liver disease, hepatic fibrosis

Secondary uses
Idiopathic pulmonary fibrosis, primary biliary cholangitis, primary sclerosing cholangitis
Research status
Phase 2 development; Phase 2b clinical study is being investigated in biopsy-confirmed MASH subjects with fibrosis.
FDA status
FDA granted fast track designation for MASH treatment. Received orphan drug designation from FDA and EMA for idiopathic pulmonary fibrosis, primary biliary cholangitis, and primary sclerosing cholangitis.

albiglutide

Moderate

How it works:

aleniglipron

Moderate

How it works:

Bimagrumab

aka BYM338

ModeratePhase 2

How it works: Bimagrumab (BYM338) is a fully human IgG1 monoclonal antibody that blocks activin type II receptors (ActRIIA and ActRIIB), inhibiting myostatin, activin A, and other TGF-beta superfamily ligands that suppress muscle growth. Originally developed by Novartis, licensed to Versanis Bio, then acquired by Eli Lilly for up to $1.925 billion in 2023. Phase 2 trials demonstrated simultaneous fat mass loss

Body composition improvement (fat loss with muscle preservation); Combination therapy with GLP-1 receptor agonists for obesity; Sarcopenia research (age-related muscle loss); Inclusion body myositis (failed primary endpoint in RESILIENT); Muscle wasting conditions (COPD, hip fracture recovery)

Administration

IV

Timing

Administered as IV infusion at clinical sites. The BELIEVE trial used approximately Q12W dosing (4 infusions over 48 weeks) in combination with semagl

Cycle length

48 weeks

Half-life
Approximately 19 days in humans, consistent with typical IgG1 monoclonal antibod
Contraindications
Bimagrumab has not been approved for any indication. Formal contraindications ha; Conditions involving TGF-beta superfamily signaling (e.g., hereditary hemorrhagi; Pregnancy and breastfeeding, as activin signaling plays critical roles in reprod
Research status
Phase 2
FDA status
Not approved
Legal status
US: Investigational
Research evidence
moderate
Indications
Body composition improvement (fat loss with muscle preservation); Combination therapy with GLP-1 receptor agonists for obesity; Sarcopenia research (age-related muscle loss); Inclusion body myositis (failed primary endpoint in RESILIENT); Muscle wasting conditions (COPD, hip fracture recovery)
Chemical data
Complex immunoglobulin · 145000 Da
Amino acids
445 aa

Bivamelagon

aka LB54640

ModeratePhase 2

How it works: Bivamelagon (LB54640) is an oral small molecule melanocortin-4 receptor (MC4R) agonist developed by Rhythm Pharmaceuticals (licensed from LG Chem) for hypothalamic obesity in patients aged 12 and older. In a Phase 2 trial, bivamelagon achieved 9.3% BMI reduction at 600 mg and 7.7% at 400 mg over 14 weeks, with significant hunger score reductions. It is the first oral MC4R agonist in clinical devel

Hypothalamic obesity (ages 12 and older); Obesity related to hypothalamic dysfunction

Administration

Oral

Timing

Once-daily oral tablet. Significant practical advantage over setmelanotide, which requires daily subcutaneous injections.

Cycle length

14 weeks (Phase 2 trial)

Half-life
Not publicly disclosed (supports once-daily oral dosing)
Contraindications
Investigational compound: not approved for clinical use; Expected caution in patients with conditions affected by melanocortin signaling; Drug interactions not fully characterized. As a small molecule with CNS penetrat
Research status
Phase 2
FDA status
Not approved
Legal status
US: Investigational
Research evidence
low
Indications
Hypothalamic obesity (ages 12 and older); Obesity related to hypothalamic dysfunction
Chemical data
C35H53ClN4O4 · 629.3 Da
Amino acids
43 aa

eloralintide

Moderate

How it works:

Enobosarm

aka Ostarine, GTx-024, MK-2866

ModeratePhase 2b

How it works: Enobosarm (Ostarine, GTx-024, MK-2866) is an oral nonsteroidal selective androgen receptor modulator (SARM) being developed by Veru Inc. for muscle preservation during GLP-1 receptor agonist-induced weight loss. In the Phase 2b QUALITY trial, enobosarm 3 mg combined with semaglutide eliminated lean mass loss (0% lean mass loss, 100% fat mass loss) and preserved physical function in older adults. T

Muscle preservation during GLP-1 receptor agonist weight loss therapy; Lean body mass improvement in elderly (investigational); Cancer-associated muscle wasting (prior clinical program)

Administration

Oral

Timing

Once daily oral administration; no specific timing requirement reported

Cycle length

16-72 weeks (trial dependent)Step-wise Titration

Half-life
Approximately
Storage
Dry: Controlled room temperature (15-30 degrees C)
Contraindications
Known hypersensitivity to enobosarm or any excipient; Pregnancy and breastfeeding (androgen receptor modulation may cause fetal harm); Hormone-sensitive cancers (androgen receptor activation may stimulate tumor grow; Active liver disease or significantly elevated liver enzymesFrequency distributi
Research status
Phase 2b
Legal status
US: Investigational
Research evidence
moderate
Indications
Muscle preservation during GLP-1 receptor agonist weight loss therapy; Lean body mass improvement in elderly (investigational); Cancer-associated muscle wasting (prior clinical program)
Chemical data
CAS 841205-47-8 · C19H14F3N3O3 · 389.33 Da
Amino acids
48 aa

gubamy

Moderate

How it works:

MET-097i

aka PF-3944, MET-097

ModeratePhase 2b

How it works: MET-097i (PF-3944) is an ultra-long-acting GLP-1 receptor agonist developed using Metsera's proprietary HALO (Half-life Augmented Linker and Oligomer) platform. With a half-life of approximately 380 hours, it enables once-monthly subcutaneous dosing. In Phase 2b (VESPER-3), a weekly-to-monthly transition protocol achieved 12.3% weight loss at 28 weeks. Pfizer acquired Metsera for approximately $10

Obesity and overweight with comorbidities; Type 2 diabetes (potential future indication)

Administration

SC

Timing

Weekly-to-monthly transition protocol used in clinical trials; initial weekly dosing before transitioning to once-monthly injection

Cycle length

28 weeks (Phase 2b)

Half-life
for monthly GLP-1 agonism.","url":"https://www.peptideprotocolwiki.com/peptides/
Contraindications
Investigational compound: not approved for clinical use; Expected class contraindications based on GLP-1 receptor agonist class including; Drug interactions not fully characterized. GLP-1 receptor activation delays gast
Research status
Phase 2b
Legal status
US: Investigational
Research evidence
low
Indications
Obesity and overweight with comorbidities; Type 2 diabetes (potential future indication)
Chemical data
Proprietary (not publicly disclosed) · 4500 Da
Amino acids
66 aa

Petrelintide

aka ZP8396

ModeratePhase 1b

How it works: Petrelintide (ZP8396) is a 36-amino acid acylated amylin analog developed by Zealand Pharma and licensed to Roche in a deal worth up to $5.3 billion. Designed for once-weekly subcutaneous administration, it restores amylin signaling to reduce appetite and promote weight loss. In Phase 1b, 8.6% body weight loss was observed at 4.8 mg over 16 doses. Phase 2b ZUPREME trials are underway.New to metabo

Obesity and overweight with comorbidities; Potential combination therapy with GLP-1 receptor agonists

Administration

SC

Timing

Dose escalation protocol used in Phase 1b; ZUPREME Phase 2b trials evaluating optimized dosing

Cycle length

16 doses (Phase 1b)

Half-life
Approximately 4-7 days (supports once-weekly dosing)
Contraindications
Investigational compound: not approved for clinical use; Expected caution in patients with gastroparesis or severe gastrointestinal motil; Drug interactions not fully characterized. Amylin analogs slow gastric emptying,
Research status
Phase 1b
Legal status
US: Investigational
Research evidence
low
Indications
Obesity and overweight with comorbidities; Potential combination therapy with GLP-1 receptor agonists
Chemical data
C185H305N49O61 · 4170 Da
Amino acids
55 aa

Ribupatide

aka HRS9531, KAI-9531, HRS-9531

ModeratePhase 3

How it works: Ribupatide (HRS9531/KAI-9531) is a dual GLP-1/GIP receptor agonist developed by Hengrui Pharma (China) and Kailera Therapeutics (global). It is being developed in both injectable and oral formulations. In Phase 2, the injectable 8 mg dose achieved 21.1% placebo-adjusted weight loss at 36 weeks with 59% of participants losing 20% or more. The oral formulation achieved 12.1% weight loss at 26 weeks.

Chronic weight management in adults with obesity or overweight; Potential type 2 diabetes treatment (under investigation)

Administration

SC

Timing

Dose escalation used to minimize GI side effects. Both injectable and oral formulations are under investigation.

Cycle length

26-36 weeks (Phase 2 trials)

Half-life
Suitable for once-weekly injection (specific value not disclosed)
Contraindications
Investigational compound: not approved for clinical use; use only within clinica; Expected class contraindications: personal or family history of medullary thyroi; Pregnancy and breastfeeding (expected contraindication based on class)Frequency; Insulin and sulfonylureas: increased hypoglycemia risk expected based on GLP-1/G
Research status
Phase 3
FDA status
Not approved
Legal status
US: Investigational
Research evidence
moderate
Indications
Chronic weight management in adults with obesity or overweight; Potential type 2 diabetes treatment (under investigation)
Chemical data
Proprietary (not disclosed) · 4800 Da
Amino acids
22 aa

Survodutide

aka BI 456906

ModeratePhase 3

How it works: Survodutide (BI 456906) is a dual glucagon receptor (GCGR) and GLP-1 receptor agonist developed by Boehringer Ingelheim currently in Phase 3 clinical trials for obesity and MASH/NASH. It uniquely combines GLP-1 signaling for appetite suppression with glucagon signaling for increased energy expenditure.New to metabolic peptides?Browse all metabolic peptides →Table of Contents📌TL;DR•Dual GLP-1/gluc

Obesity treatment (Phase 3); MASH/NASH therapy; Metabolic syndrome research; Type 2 diabetes investigation

Administration

SC

Timing

Same day each week, any time of day✓ Rotate injection sites

Cycle length

46-48 weeks in Phase 2 trials (chronic therapy expected)Step-wise Titration

Half-life
Approximately 6-7 days (estimated from weekly dosing)
Storage
Dry: Storage conditions for survodutide in clinical trials have not been publicly detailed. Based on the pharmacological class and lipid-modified peptide f
Contraindications
Personal or family history of medullary thyroid carcinoma (MTC) or Multiple Endo; Severe gastrointestinal disease including gastroparesis, inflammatory bowel dise; Pregnancy (incretin-based therapies may cause fetal harm based on animal data; s
Research status
Phase 3
FDA status
Not approved
Legal status
US: Investigational
Research evidence
moderate
Indications
Obesity treatment (Phase 3); MASH/NASH therapy; Metabolic syndrome research; Type 2 diabetes investigation
Chemical data
CAS 2375568-58-4 · C192H289N47O61 · 4231.62 Da
Amino acids
262 aa

taspoglutide

Moderate

How it works:

Trevogrumab

aka REGN1033, REGN-1033, SAR-391786

ModeratePhase 2

How it works: Trevogrumab (REGN1033) is a fully human IgG4 monoclonal antibody that selectively binds and neutralizes myostatin (GDF-8), the primary negative regulator of skeletal muscle mass. Developed by Regeneron Pharmaceuticals, it is being evaluated in the Phase 2 COURAGE trial in combination with semaglutide for preserving lean mass during weight loss in patients with obesity. At 26 weeks, adding trevogru

Lean mass preservation during GLP-1 agonist therapy for obesity; Potential treatment for sarcopenia and muscle wasting conditions; Body composition optimization during weight loss

Administration

SC

Timing

Administered in combination with semaglutide 2.4 mg SC weekly in the COURAGE trial. Clinical trial setting only.

Cycle length

26-week weight-loss phase followed by 26-week maintenance

Half-life
Specific half-life not publicly reported. As an IgG4 antibody, the expected half
Contraindications
Trevogrumab has not been approved for any indication. Formal contraindications h; Pregnancy and breastfeeding, as myostatin signaling may play roles in fetal musc; Conditions requiring maintained myostatin signaling for physiological balance (t; GLP-1 receptor agonists (semaglutide
Research status
Phase 2
FDA status
Not approved
Legal status
US: Investigational
Research evidence
moderate
Indications
Lean mass preservation during GLP-1 agonist therapy for obesity; Potential treatment for sarcopenia and muscle wasting conditions; Body composition optimization during weight loss
Chemical data
CAS 1429201-24-0 · Complex immunoglobulin · 150000 Da
Amino acids
221 aa

Zovaglutide

aka ZT-002

ModeratePhase 2

How it works: Zovaglutide (ZT-002) is a novel GLP-1 receptor agonist featuring a dual-fatty acid chain design that enables once-monthly subcutaneous dosing. In phase 2 trials, the 160 mg monthly dose achieved 13.8% body weight reduction at 24 weeks, with only 1.3% GI-related discontinuation. Developed by QL Biopharm, it has advanced to phase 3.New to metabolic peptides?Browse all metabolic peptides →Table of Co

Obesity and overweight (weight management); Type 2 diabetes (potential future indication)

Administration

SC

Timing

Monthly subcutaneous injection with dose escalation✓ Rotate injection sites

Cycle length

OngoingStep-wise Titration (8 weeks)

Half-life
pharmacokinetics, and GLP-1 receptor binding.","url":"https://www.peptideprotoco
Storage
Dry: Likely refrigerated (2-8 degrees C). Consult product-specific guidance.
Contraindications
Known hypersensitivity to zovaglutide or any excipient (presumed based on GLP-1; Personal or family history of medullary thyroid carcinoma or MEN2 (GLP-1 RA clas; History of pancreatitis (GLP-1 RA class precaution)Frequency distribution of rep; Potential to slow gastric emptying, which may affect absorption of concomitant o
Research status
Phase 2
FDA status
Not approved
Legal status
US: Investigational
Research evidence
low
Indications
Obesity and overweight (weight management); Type 2 diabetes (potential future indication)
Chemical data
Proprietary (not publicly disclosed) · 4500 Da
Amino acids
89 aa

Example stacks

Beginner

Fat Loss - Beginner

A clean single-compound starting point. AOD-9604 targets fat breakdown directly without the complexity of a full GH stack.

Primary
AOD-9604300 mcg/day - Fasted AM pre-workout
  • • Inject fasted - 2-3 hrs after last meal
  • • Stay in a caloric deficit
  • • Give it 6+ weeks before assessing
Intermediate

Fat Loss - Intermediate

Combines appetite suppression via semaglutide with targeted lipolysis from AOD-9604. Two different mechanisms working together.

Primary
Semaglutide0.25 mg/week, titrate up - Once weekly, any time
Support
AOD-9604300 mcg/day - Fasted AM
  • • Titrate semaglutide slowly - increase every 4 weeks if tolerated
  • • Stay well hydrated throughout
  • • Track muscle mass alongside body weight

Community outcome data

Collected from users researching this goal. Not a clinical database - for general reference only.

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