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Latest update: 2026-10-27 · 93 recorded entries

Review history

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October 2026

Argireline: what wrinkle studies show

Learn what Argireline is, what small wrinkle trials measured, and why a laboratory skin-penetration result cannot predict every serum's effects.

Is tesofensine a peptide?

Is tesofensine a peptide? Check its recorded structure, learn what reuptake inhibitor means, and separate a substance identifier from drug approval.

Tirzepatide

Updated the Mounjaro source to its August 2026 label and checked its approved uses and eye warning. Zepbound remains a separate product record.

Is glucagon a peptide?

Yes. Glucagon is a peptide hormone that helps raise blood sugar. Learn its normal role and how it differs from proglucagon and GLP-1.

Is somatostatin a peptide?

Yes. Human somatostatin has 14- and 28-amino-acid peptide forms. Compare both with their 116-unit precursor and with octreotide.

Is ghrelin a peptide?

Yes. Human ghrelin has 28- and 27-unit peptide forms. See how its 117-unit precursor and a fatty-acid change affect the names in source records.

September 2026

Is calcitonin a peptide?

Yes. Human calcitonin is a 32-unit peptide hormone. Learn why its precursor has 141 units and how calcitonin differs from procalcitonin and CGRP.

Is vasopressin a peptide?

Yes. Human vasopressin is a nine-unit peptide hormone. See why its precursor has 164 units and how vasopressin differs from copeptin and oxytocin.

Is insulin a peptide?

Yes. Human insulin is a peptide hormone also described as a small protein. See how its two chains differ from proinsulin and C-peptide.

Is GLP-1 a peptide?

Yes, GLP-1 is a peptide hormone. Compare its 30- and 31-unit forms with its precursor, semaglutide, and a nonpeptide receptor agonist.

Is collagen a peptide?

Collagen is a protein made of peptide-linked chains. Learn how intact collagen, gelatin, and collagen peptides differ, and what each name can tell you.

Is glutathione a peptide?

Is glutathione a peptide? Learn why glutathione is a tripeptide, how its unusual bond works, and what chemical class cannot tell you.

Is SLU-PP-332 a peptide?

Is SLU-PP-332 a peptide? Learn what its chemical structure shows and why a catalog label cannot establish chemical class.

Is carnosine a peptide?

Is carnosine a peptide? Learn how its two amino-acid units determine its chemical class and what that class cannot show.

Is creatine a peptide?

Is creatine a peptide? Learn why creatine is an amino-acid derivative rather than an amino-acid chain.

Is taurine a peptide?

Is taurine a peptide? Learn why taurine is an amino sulfonic acid rather than an amino-acid chain.

Is melatonin a peptide?

Is melatonin a peptide? Learn why melatonin is an indoleamine rather than an amino-acid chain.

Is oxytocin a peptide?

Is oxytocin a peptide? Learn why oxytocin is a cyclic nine-amino-acid peptide and what that class cannot show.

Is MK-677 a peptide?

Is MK-677 a peptide? Learn why ibutamoren is a nonpeptide, what its receptor studies show, and where FDA status and safety evidence stop.

Is NAD a peptide?

Is NAD a peptide? Learn why NAD is a dinucleotide coenzyme and how NAD+, NADH, NMN, and NR differ from peptides.

Oral peptides: do peptide pills work?

Most oral peptides break down when swallowed. See which FDA-approved peptide pills are built to work, what their studies measured, and how to check a peptide pill claim.

Tirzepatide

Checked the posted Mounjaro and Zepbound labels against their August supplement letters and clarified which product has each approved use.

VIP peptide

Reviewed the discovery report, a 12-person healthy-volunteer study, the 196-person aviptadil trial, and exact FDA substance and orphan-designation records. This is an internal source review, not independent medical review.

August 2026

Semaglutide

Checked current Ozempic, Rybelsus, and Wegovy labels. Added the Wegovy injection use for MASH, kept each form's limits, and checked the 2026 sports monitoring record.

Insulin

Checked the current Humalog label, the main DCCT results, and the 2026 WADA rule for insulin. Kept the product and study limits.

Tirzepatide

Updated Mounjaro and Zepbound label records, added the Mounjaro heart-risk approval and Zepbound supplement, and linked the FDA structure review.

Cagrilintide

Reviewed the cagrilintide-alone phase 2 study and the later large CagriSema study. Also reviewed a study that measured how the body processed and responded to cagrilintide given with semaglutide. Checked current study records and FDA's cagrilintide statement.

SS-31

Reviewed FDA's Forzinity approval, label, and trial summary, the FDA identity record, and randomized human studies in Barth syndrome, primary mitochondrial myopathy, heart failure, and healthy older adults.

Cerebrolysin

Initial brief reviewed FDA identity and orphan-designation records, Austrian product information, randomized human trials, composition studies, and the 2026 World Anti-Doping Agency list.

Kisspeptin-10

Initial brief reviewed FDA identity and compounding records, small human hormone studies, and the 2026 World Anti-Doping Agency list.

Thymosin alpha-1

Initial brief reviewed FDA identity and compounding records, randomized human trials, corrected sepsis results, and the 2026 World Anti-Doping Agency list.

Gonadorelin

Initial brief reviewed FDA identity and approval records, human studies, and current animal-product status. It also checked a 2026 FDA warning letter and the 2026 World Anti-Doping Agency list.

GHRP-6

Initial brief reviewed FDA identity and compounding records, small human hormone and exposure studies, the FDA approval database, and the 2026 World Anti-Doping Agency list.

Semax

Reviewed FDA's 2026 Semax briefing and advisory-committee record, FDA's substance record, human stroke and brain-scan studies, and the chemical record for N-acetyl Semax amidate.

Selank

Initial brief reviewed FDA identity, approval, and compounding records, three small anxiety studies, and a human brain-scan study.

DSIP

Initial brief reviewed FDA identity and compounding records, the July 2026 advisory-committee record, and small human studies of sleep, hormone changes, narcolepsy, and withdrawal symptoms.

LL-37

Initial review covered FDA records and human studies of leg ulcers, melanoma, and COVID-19. It also covered FDA's planned advisory-committee discussion.

P21 peptide

Initial brief reviewed the FDA chemical record, primary animal and cell studies, the p21/CDKN1A name conflict, a ClinicalTrials.gov search for P021, and FDA drug-approval databases.

Peptides and steroids: what is different, what is not

A plain-language comparison of peptides and steroids. It covers chemistry, how they send signals, approved medicines, product quality, safety evidence, and the 2026 World Anti-Doping Agency list.

CJC-1295

Clarified the human hormone findings, product-form limits, FDA safety record, and 2026 anti-doping status.

Semaglutide

Revalidated the semaglutide approval claim against the current Wegovy label and retained product-, formulation-, population-, and indication-specific scope.

BPC-157

Revalidated BPC-157's S0 prohibited-at-all-times status against the 2026 WADA Prohibited List.

Retatrutide

Revalidated FDA approval status, the boundary between trial material and online products, and the distinction between a planned 2027 submission and approval or availability.

Tesamorelin

Revalidated the current Egrifta WR indication and weight-loss limitation against FDA labeling, and confirmed tesamorelin remains named on the 2026 WADA Prohibited List.

TB-500

Revalidated TB-500 against the 2026 WADA Prohibited List, where TB-500 and thymosin-beta-4 are named in the prohibited growth-factor category.

Bremelanotide

Revalidated the Vyleesi indication and limits against FDA labeling. The approved use is limited to certain premenopausal women with acquired, generalized hypoactive sexual desire disorder (HSDD). The label says it is not for sexual-performance enhancement.

July 2026

Retatrutide

Registered the Phase 3 and submission-plan statements as scoped claim records and split the TRIUMPH-1 and TRIUMPH-2/3 disclosure dates. No new evidence was reviewed.

Melanotan II

Initial brief reviewed the 1996 and 2000 human studies and published case reports. One case report describes a prolonged painful erection that needed emergency treatment after Melanotan II use. The brief also used product-analysis data and two approved melanocortin labels only for contrast. Case reports show reported events, not how often they happen or what caused them.

Retatrutide

Added Lilly's July 2026 early sponsor-reported Phase 3 results. Rechecked that retatrutide remained under study and not FDA-approved. Also checked the limits for products sold under its name.

Semaglutide

Expanded product, claim, and source provenance fields.

Insulin

Expanded product, safety, and claim source details.

Tirzepatide

Expanded product, outcome, and unapproved-version boundaries.

BPC-157

Updated around FDA's July 2026 briefing and explicit product-identity boundaries.

CJC-1295

Expanded alias, product-identity, and anti-doping context.

Ipamorelin

Expanded trial-outcome, route, and product-quality boundaries.

Liraglutide

Initial brief based on the current Saxenda label, LEADER, and FDA product records.

Retatrutide

Checked against the phase 2 publication and the June 2026 TRIUMPH-1 registry update: study complete, no summary results posted.

Tesamorelin

Updated for Egrifta SV and Egrifta WR product identity, non-substitutability, phase 3 outcomes, and the 2026 WADA list.

Sermorelin

Updated with FDA's 2013 determination that the discontinued Geref products were not withdrawn for safety or effectiveness.

TB-500

Initial brief uses FDA's July 2026 identity and evidence review before final agency action.

GHK-Cu

Initial brief separates topical formulation studies from injectable-product claims.

MOTS-c

Initial brief reflects FDA's July 2026 evidence review before final agency action.

AOD-9604

Initial brief based on FDA's 2024 compounding review and current safety-risk page.

Epitalon

Initial brief reflects FDA's July 2026 insomnia-focused evidence review before final agency action.

Bremelanotide

Initial brief based on the Vyleesi label, RECONNECT trials, and FDA multidisciplinary review.

Afamelanotide

Initial brief based on the current Scenesse label, pivotal trials, and orphan-drug record.

Teriparatide

Initial brief based on the current Forteo label and fracture-prevention trial record.

Abaloparatide

Initial brief based on the 2025 Tymlos label and ACTIVE phase 3 trial.

Teduglutide

Initial brief based on the 2025 Gattex label, randomized trial, and orphan-drug record.