ThePeptide Examiner
Obesity drug pipeline

Every obesity drug candidate in clinical development.

Approved drugs, submitted filings, Phase 3 and Phase 2 candidates — with mechanism, latest readouts, and primary-source citations. Updated as data lands.

Editorially reviewedThe Peptide Examiner editorial team, Editorial review · Reviewed Apr 23, 2026
DrugDeveloperMechanismPhase
TirzepatideMounjaro / Zepbound
Eli LillyDual GIP / GLP-1 receptor agonistApproved
SemaglutideOzempic / Wegovy / Rybelsus
Novo NordiskGLP-1 receptor agonistApproved
Novo NordiskAmylin analog + GLP-1 receptor agonist (fixed-dose combination)Submitted
OrforglipronFoundayo (expected)
Eli LillySmall-molecule GLP-1 receptor agonist (oral)Submitted
RetatrutideLY-3437943
Eli LillyTriple GIP / GLP-1 / glucagon receptor agonistPhase 3
SurvodutideBI 456906
Boehringer Ingelheim / Zealand PharmaDual GLP-1 / glucagon receptor agonistPhase 3
PemvidutideALT-801
AltimmuneDual GLP-1 / glucagon receptor agonistPhase 2b
Amycretin
Novo NordiskSingle-molecule amylin / GLP-1 dual agonist (injectable + oral variants)Phase 2
DanuglipronPF-06882961
PfizerSmall-molecule GLP-1 receptor agonist (oral)Phase 2

Tirzepatide

Eli Lilly · Approved

Latest readout: SURMOUNT-5 head-to-head vs semaglutide (NEJM 2025)

What's next: Approved — ongoing indication expansions (HFpEF, CKD, NASH)

Semaglutide

Novo Nordisk · Approved

Latest readout: SELECT cardiovascular benefit (NEJM 2023)

What's next: Approved — ongoing indication expansions (HFpEF, CKD, Alzheimer's)

Retatrutide

Eli Lilly · Phase 3

Latest readout: Phase 2 (NEJM 2023): ~24.2% mean weight loss at 48 weeks on 12 mg

What's next: Phase 3 TRIUMPH readouts 2025–2026; FDA filing 2026; approval 2026–2027

Survodutide

Boehringer Ingelheim / Zealand Pharma · Phase 3

Latest readout: Phase 2 (Lancet 2023): ~19% weight loss at 46 weeks on highest dose

What's next: Phase 3 SYNCHRONIZE readouts 2025–2026

Pemvidutide

Altimmune · Phase 2b

Latest readout: MOMENTUM Phase 2: ~15.6% weight loss at 48 weeks on 2.4 mg

What's next: Phase 3 entry 2025–2026

Danuglipron

Pfizer · Phase 2

Latest readout: Phase 2 results variable; Pfizer discontinued twice-daily formulation in 2023; once-daily formulation ongoing

What's next: Uncertain — Pfizer's oral GLP-1 path has hit multiple tolerability issues