Reference
Compare peptides
Two to four compounds, field by field: identity, United States regulatory status, and what kinds of documents are on file. The table records differences. It does not rank them.
No winner, no score, no recommendation. Counts describe how many documents of each kind Therapept has indexed — not how well a compound works, and not how much has been published overall.
Link to this comparison: /compare?peptides=sm04554,retatrutide,cagrilintide
| SM04554 | Retatrutide | Cagrilintide | |
|---|---|---|---|
| Identity | |||
| Class | Investigational topical small-molecule modulator of Wnt signalling | Investigational triple agonist of GIP, GLP-1 and glucagon receptors | Investigational long-acting acylated amylin analogue |
| Also listed as | Dalosirvat, SM-04554 | LY3437943, LY-3437943 | Not recorded |
| Molecular formula | Not recorded | Not recorded | C194H312N54O59S2 |
| Molecular weight | Not recorded | 4731.33 g/mol (average mass, widely cited for the free base) | 4409 g/mol |
| CAS | Not recorded | 2381089-83-2 | 1415456-99-3 |
| PubChem CID | Not recorded | Not recorded | 171397054 |
| Sequence length | Not recorded | Not recorded | Described structurally, not as a residue list |
| Data caveat | None recorded | PubChem’s retatrutide record states a CID is not available as a discrete structure. Full caveat | None recorded |
| United States regulatory status | |||
| Status | Investigational | Investigational | Investigational |
| FDA application | None recorded | None recorded | None recorded |
| Compounding | No FDA compounding entry recorded | No FDA compounding entry recorded | No FDA compounding entry recorded |
| WADA | Not named in this record | Not named in this record | Not named in this record |
| Research profile | |||
| Research purpose | Wnt-pathway modulation | Triple-agonist metabolic research | No plain-English profile recorded |
| Proposed mechanism | Proposed activation of Wnt/beta-catenin signalling in the follicle, promoting follicle proliferation. The trial protocol itself flags theoretical pathway-related risks. | Proposed triple agonism: GLP-1 and GIP effects on appetite and insulin, plus glucagon-receptor signalling in the liver and energy expenditure. The net clinical contribution of each arm is still being studied. | No plain-English profile recorded |
| Human evidence | Phase 1 and Phase 2 trials were registered and completed. Therapept did not identify an active later-stage registration or an approved product at review. | A published 48-week Phase 2 trial in 338 adults, plus Phase 3 trials registered and sponsor topline disclosures. No approved product exists. | No plain-English profile recorded |
| Evidence tier | Phase 2 trials registered or reported | Phase 3 trials registered or reported | No plain-English profile recorded |
| Known safety concerns |
|
| No plain-English profile recorded |
| Evidence gaps |
|
| No plain-English profile recorded |
| Head-to-head evidence | No published head-to-head trial against minoxidil or any other treatment. | No published head-to-head trial against semaglutide or tirzepatide. Cross-trial comparisons are not head-to-head evidence. | No plain-English profile recorded |
| Named pathways | Wnt/beta-catenin signalling · Follicle proliferation · Hair cycle | GIP receptor · GLP-1 receptor · Glucagon receptor · Hepatic lipid oxidation · Energy expenditure | No plain-English profile recorded |
| Evidence on file | |||
| Records | |||
| Human-interventional records | 1 | 2 | 0 |
| Human-observational records | 0 | 0 | 0 |
| Animal records | 0 | 0 | 0 |
| In-vitro records | 0 | 0 | 0 |
| Reviews | 0 | 0 | 0 |
| Regulatory documents | 0 | 0 | 0 |
| Earliest indexed | 2019 | 2023 | Not recorded |
| Latest indexed | 2019 | 2026 | Not recorded |
Every identity and regulatory value above is taken from the compound’s record, where its sources are listed. Evidence counts are derived from the published evidence file at build time. A missing class means no document of that kind is indexed — not that none exists.
