Development trackerPipeline
Development tracker
Pipeline
Where each compound actually sits — from FDA-approved drugs to gray-market research chemicals with no formal development at all. Dated, factual, no hype.
FDA-approved4
SemaglutideA
Preclinical
Phase 1
Phase 2
Phase 3
Approved
Multiple large RCTs; SELECT 20% MACE reduction; MASH accelerated approval (Aug 2025). Tirzepatide beats it on weight loss.
TirzepatideA
Preclinical
Phase 1
Phase 2
Phase 3
Approved
Strongest dataset of any catalog peptide (SURPASS-CVOT n=13,299: non-inferior, NOT superior to dulaglutide; superiority P=0.09). +OSA approval Dec 2024.
PT-141 (Bremelanotide)A
Preclinical
Phase 1
Phase 2
Phase 3
Approved
RECONNECT (n=1,267) met co-primaries with MODEST effect; did NOT increase satisfying sexual events. Men's use is Phase 2 at best / off-label.
TesamorelinA
Preclinical
Phase 1
Phase 2
Phase 3
Approved
Approved for HIV-lipodystrophy only (~10-11% VAT reduction at 26 wks; '15-18%' overstates pivotal endpoints). Anti-aging use is extrapolation.
In clinical trials2
RetatrutideB
Preclinical
Phase 1
Phase 2
Phase 3
Approved
Late Phase 3 topline (company press release; not peer-reviewed). Dose-dependent dysesthesia (~21% high dose); cardiac arrhythmia signal in Phase 2.
Cagrilintide / CagriSemaB
Preclinical
Phase 1
Phase 2
Phase 3
Approved
Multiple completed Phase 3 RCTs (REDEFINE 1/2 strong; REDEFINE 4 missed non-inferiority vs tirzepatide). Not approved.
Research / gray-market — no formal FDA pipeline12
DBPC-157Removed from Cat 2 · pending PCACBGHK-CuRemoved from Cat 2 · pending PCACDTB-500 (Thymosin beta-4 fragment)Removed from Cat 2 · pending PCACBCJC-1295 / IpamorelinRemoved from Cat 2 · pending PCACBSermorelinResearch-use-only — gray marketDMOTS-cRemoved from Cat 2 · pending PCACEEpitalon (Epithalon)Removed from Cat 2 · pending PCACBSelankCategory 2 — restrictedBSemaxRemoved from Cat 2 · pending PCACENAD+ (and precursors NMN/NR)Research-use-only — gray marketBMelanotan IIBanned / prohibitedDKPVRemoved from Cat 2 · pending PCAC
Regulatory status reflects the 2026 FDA docket (FDA-2025-N-6895) and moves often — re-verify before acting. Not medical or legal advice.