STEP showed 14.9% weight loss at 68 weeks in obesity. SELECT showed 20% reduction in major adverse cardiovascular events in patients with overweight/obesity + established CVD — the first weight-loss drug with proven CV outcome data.
Source →Semaglutide
Monograph · ASemaglutide
Long-acting GLP-1 receptor agonist. GLP1R variants (rs6923761) modulate weight-loss response.
How it clearsHalf cleared in ~7d. Most (~96%) gone by ~35d.

Modified GLP-1(7-37) with fatty-acid acylation for albumin binding (≈1 week half-life). STEP trials show 15-17% body weight reduction at 68 weeks. SELECT trial extends evidence to cardiovascular outcomes in non-diabetics.
Cohort curves show movement — your n=1 often lags the median by one check-in cycle. The gap between "I should feel it" and "labs show it" is where most people quit early. Metabolic compounds still need lifestyle structure; modest results without it are mechanism, not failure.
Compounded semaglutide (gray market) is no longer permitted by FDA after the shortage ended (2024). Verify your source's legal posture. Same GI titration requirement as tirzepatide.
Aib at position 2; C18 fatty acid conjugated at K20 via γGlu-2×OEG linker.
Known risk or pharmacological conflict.
Upload your data to see how it relates to Semaglutide.
Upload a lab file (LabCorp / Quest) or DNA file (23andMe / AncestryDNA). Stack will show your specific markers alongside the literature-reported response windows.
Upload in /historyStack doesn't rank peptides — we surface the diversity of opinion. Each card paraphrases a public-record stance from a named source. Where they conflict is where you should slow down and read both.
Useful tool for the metabolic-syndrome end of obesity but argues GLP-1s shouldn't substitute for fixing the food environment. Concerned about long-term dependence and post-discontinuation rebound. Critical of telehealth chains that prescribed without metabolic workup.
Per-claim grading. Each claim is graded independently — same peptide, different claims can carry different grades.
- AStrong evidence
Semaglutide produces ~15% mean body weight reduction at 68 weeks (vs ~2% placebo) in adults with obesity
1 supporting referencesVerified 50d ago - AStrong evidence
Semaglutide reduces major adverse cardiovascular events in adults with overweight/obesity and CV disease
1 supporting referencesVerified 50d ago - AStrong evidence
Semaglutide reduces HbA1c by ~1.5-1.8% in adults with type 2 diabetes
1 supporting referencesVerified 50d ago
External links to PubMed searches, ClinicalTrials.gov, and FDA materials. We do not host papers — we point at canonical sources.
- RegulatoryENREGULATORYFunding undisclosedVerified 23d agoFDA Wegovy label
- ReviewENRCTIndustry-fundedVerified 50d agoSTEP trials review
- RegulatoryEUREGULATORYFunding undisclosedVerified 23d agoEMA Wegovy EPAR (European Medicines Agency)
- ReviewESREVIEWFunding undisclosedVerified 23d agoSciELO — semaglutida (Latin American clinical literature)
FDA approved (Ozempic / Wegovy)
FDA declares Semaglutide shortage resolved — compounding ends
FDA declared the Semaglutide shortage resolved in May 2025. Compounded Semaglutide (sold as 'Wegovy alternatives' by telehealth chains) is no longer permitted in the US. The shutdown applied to both 503A and 503B pharmacies.
COFEPRIS issues counterfeit-Ozempic warning amid cross-border GLP-1 demand
COFEPRIS issued formal warnings about counterfeit Ozempic, Wegovy, and Saxenda circulating in Mexican gray markets, particularly in border-state pharmacies catering to US cross-border traffic. Several seizures documented in Tijuana, Juárez, and Reynosa.
Semaglutide (Wegovy) approved for cardiovascular risk reduction
FDA approved an expanded label for Semaglutide (Wegovy) to reduce risk of cardiovascular death, heart attack, and stroke in adults with overweight/obesity + established cardiovascular disease. Based on the SELECT trial.
Mexico (COFEPRIS) maintains GLP-1 prescription regime through obesity epidemic
COFEPRIS (Mexican federal health regulator) continued to require physician prescription for GLP-1 agonists through 2023-2024 despite high obesity prevalence and pharmacy-tourism demand from US patients. Compounding less restrictive than US 503A regime.
Argentina (ANMAT), Colombia (INVIMA), Brazil (ANVISA) — LATAM GLP-1 access landscape
ANMAT (Argentina), INVIMA (Colombia), and ANVISA (Brazil) all regulate GLP-1 agonists as prescription drugs. Brazil is the strictest enforcement jurisdiction in LATAM. Argentina has a more porous regime in practice. Colombia sits in the middle. Cross-border GLP-1 supply between LATAM countries is real but not as developed as US-Mexico flow.
Pre-filled with this compound's published dose range: 0.25-2.4 mg · weekly, subcutaneous
Calculator is a discussion tool. Verify reconstitution + dosing with a qualified provider. Stack is not a prescription source. Use sterile technique and inspect every vial.
How much a first cycle actually costs across the channels people use. Pick the protocol length you're considering — Stack multiplies the monthly band by cycle weeks. Same caveats apply: ranges are facts, quality varies, this is not legal advice.
Numbers reflect publicly-advertised price ranges, not vendor quotes. Insurance, prescription costs, and shipping aren't included. Channels marked unavailable are filtered out.
See pharmacies for this compound →Approximate monthly cost across the channels users actually consider — brand FDA-approved retail, US 503A compounding, Mexican pharmacies, MX farmacias magistrales, and the research-grey market. Stack lists ranges, not vendor names. Quality varies wildly across channels — see each band's note.
Dosing assumption: 1.0-1.7 mg weekly (steady-state weight-management dose)
Wegovy (obesity) and Ozempic (T2D). NovoCare direct-pay program at lower bound. Insurance coverage variable.
As of 2026-04Not currently legal in US — FDA declared shortage resolved May 2025.
As of 2026-04Ozempic + Wegovy widely available in COFEPRIS-registered MX pharmacies. Border pharmacies higher counterfeit rate.
As of 2026-04Research-grey range. Same caveats as Tirzepatide grey market.
As of 2026-04Public-source attribution across the production + distribution chain. Stack does not endorse vendors — this is who is in the chain, not which one is best.
Bachem AG
CHVERIFIEDFDA REGISTEREDSwiss-headquartered global peptide API manufacturer with FDA-registered facilities. Supplies APIs to multiple FDA-approved drug brands.
Source: Bachem — peptide API drug substance manufacturerVerified 50d agoEnogen
CNVERIFIEDFDA REGISTEREDFDA GREEN LISTChina-based peptide API maker with semaglutide and tirzepatide listed on US FDA Green List. Also certified by China NMPA, EU EDQM, South Korea MFDS.
Source: Enogen — peptide API manufacturer (FDA Green List)Verified 50d agoAmbioPharm
US/CNVERIFIEDFDA REGISTEREDFDA-inspected peptide API manufacturer with US and China facilities. 500+ chemists.
Source: AmbioPharm — peptide manufacturingVerified 50d ago
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Field reports are added as users share their real-world protocols.
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Handoff & sources
Running this compound? Log it in /history, then open Dr Passport before your visit. Methodology explains grades; the research dashboard sorts the full catalog with citations.