Every branded, FDA-track GLP-1 and incretin drug we follow, approved and in the pipeline, with what it targets, how far along it is, and what's coming next.
Last updated: Jun 7, 2026
Receptors: GLP-1GIPglucagonamylin −GIP = antagonistStage: filled = reached, dark = currentBeyond weight loss: ✓ benefit ~ early signal ⚠ harm · untested
| Molecule | Maker | Targets | Stage | Weight loss | What's next |
|---|---|---|---|---|---|
| tirzepatide Mounjaro (T2D), Zepbound (obesity, OSA) | ![]() | GIPGLP-1 | ✓ Approved | 21% | SURMOUNT-MAINTAIN & cardiovascular outcomes readouts (2026) |
| semaglutide Ozempic (injectable, T2D), Wegovy (injectable, obesity), Wegovy pill (oral semaglutide, obesity), Rybelsus (oral, T2D) | ![]() | GLP-1 | ✓ Approved | 15% | Label expansions ongoing (MASH, oral obesity dose) (2026) |
| orforglipron Foundayo | ![]() | GLP-1 | ✓ Approved | 11.2% | Medicare GLP-1 Bridge begins (2026-07-01) |
| cagrilintide + semaglutide CagriSema | ![]() | GLP-1amylin | Filed (FDA review) | 22.7% | FDA decision expected (NDA filed Dec 2025) (2026-2027) |
| retatrutide — | ![]() | GIPGLP-1glucagon | Phase 3 | 28.3% | TRIUMPH Phase 3 program readouts (2026) |
| ribupatide (KAI-9531 / HRS9531) — | ![]() | GIPGLP-1 | Phase 3 | 23.6% | KaiNETIC global Phase 3 readouts; China NMPA filing submitted (2026-2027) |
| eloralintide — | ![]() | amylin | Phase 3 | 20.1% | Phase 3 program initiated (incl. obesity + T2D, NCT07282600) (2026) |
| maridebart cafraglutide MariTide | ![]() | GLP-1−GIP | Phase 3 | 20% | MARITIME Phase 3 program underway (2026) |
| mazdutide — | ![]() | glucagonGLP-1 | Phase 3 | 16.65% | Approved in China (2025); no US filing yet (2025) |
| survodutide — | ![]() | glucagonGLP-1 | Phase 3 | 16.6% | LIVERAGE MASH Phase 3 readout expected (2026-H2) |
| VK2735 — | ![]() | GIPGLP-1 | Phase 3 | 14.7% | Phase 3 VANQUISH-1 & -2 enrollment complete; topline expected ~2027 (2026) |
| efpeglenatide — | ![]() | GLP-1 | Phase 3 | 9.8% | Korean regulatory filing for obesity (MFDS); launch targeted H2 2026 (2026) |
| brenipatide — | ![]() | GIPGLP-1 | Phase 3 | — | RENEW-ALC Phase 3 (AUD); earliest approval ~2028 (2028) |
| amycretin (INN: zenagamtide) — | ![]() | amylinGLP-1 | Phase 2 | 22% | Heading into pivotal trials (2026) |
| berobenatide (MET-097i / PF-08653944) — | ![]() | GLP-1 | Phase 2 | 14.1% | 10 pivotal Phase 3 trials in 2026; pitched as first once-monthly GLP-1, with sleep apnea + knee OA expansion planned (2026) |
| elecoglipron (AZD5004 / ECC5004) — | AstraZeneca / Eccogene | GLP-1 | Phase 2 | — | Global Phase 3 program (planned) (2026) |
| aleniglipron (GSBR-1290) — | ![]() | GLP-1 | Early / watch | 16.3% | Heading to Phase 3 (oral pill) (2026) |
| pemvidutide — | ![]() | glucagonGLP-1 | Early / watch | 15.6% | Phase 3 planning; also a positive MASH (liver) trial (2026) |
| petrelintide — | ![]() | amylin | Early / watch | 10.7% | Advancing to Phase 3; petrelintide + CT-388 combo Phase 2 starting (2026) |
| MET-233i — | ![]() | amylin | Early / watch | 8.4% | MET-233i + MET-097i once-monthly combo 12-wk topline (2026) |
| ABBV-295 (GUB014295) — | ![]() | amylin | Early / watch | 7.75% | Advancing toward Phase 2 (2026) |
| AZD6234 — | ![]() | amylin | Early / watch | — | Phase 2 weight-loss readout (2026 (H1)) |
Weight loss = peak mean result at the approved (or trial) obesity dose. Diabetes brands and lower doses come in below this; see each drug's card for the per-product breakdown.
Recent updates
- Jun 8, 2026CagriSema REIMAGINE 1-3 peer-reviewed (7 Jun 2026): REIMAGINE 1 & 2 in Lancet Diabetes & Endocrinology, REIMAGINE 3 in The Lancet. All three trials promoted reported->published with DOIs; REIMAGINE 2 confirmed superior to semaglutide 2.4 mg in T2D (A1C -1.91% vs -1.76%, weight -14.2% vs -10.2%, 43% lost >=15%).
- Jun 7, 2026Retatrutide TRIUMPH-1 full obesity data presented at ADA 2026 (n=2,339, 80 wks): -28.3% weight at 12 mg (-25.9% at 9 mg, -19.0% at 4 mg), 65.3% reached BMI <30. Secondary endpoints at 12 mg: knee-osteoarthritis pain -73.1%, obstructive sleep apnea events -60.6%, triglycerides -41%, systolic BP -12.3 mmHg. Tolerability cost: 11.3% discontinued at 12 mg for adverse events vs 4.9% placebo.
- Jun 7, 2026Retatrutide heart-rhythm early signal logged (one to watch, not a verdict): in TRANSCEND-T2D-1 (n=403 treated) 7 patients had arrhythmias and 3 had major cardiovascular events vs 0 on placebo, with pulse up ~1 bpm. Because the glucagon arm can raise heart rate, it is the receptor to monitor, but trial investigators (Bajaj, Drucker, Seeley) call the case counts too small to draw conclusions; the dedicated cardiovascular-outcomes trial reads out ~2029.
- Jun 7, 2026JAMA published two phase 3 incretin trials together: mazdutide GLORY-2 (9 mg, n=461 Chinese adults with obesity, -16.65% mean weight at 60 wks, 42% lost >=20%) and orforglipron ACHIEVE-5 (n=546, add-on to insulin glargine, HbA1c down up to 1.88% at 40 wks), with a joint editorial (Gadde/Heymsfield). GLORY-2 added to trials/papers; ACHIEVE-5 promoted reported->published. Numbers reconciled to the published JAMA figures (earlier 20.1%/2.1% press estimands replaced).
- Jun 7, 2026ADA 2026 day 3: mazdutide DREAMS-3 added (beat semaglutide head-to-head in Chinese T2D + obesity); elecoglipron (AstraZeneca/Eccogene oral GLP-1, AZD5004) added as a new pipeline molecule heading to Phase 3.
- Jun 6, 2026Retatrutide TRANSCEND-T2D-1 published in The Lancet. Early type 2 diabetes monotherapy: HbA1c down 1.94% and weight down 15.3% at 12 mg; dysesthesia milder in T2D (2-4%).
- Jun 6, 2026ADA 2026 readouts added: orforglipron ACHIEVE-2/4/5, CagriSema REIMAGINE 1-3, zenagamtide (amycretin) phase 2, survodutide SYNCHRONIZE-1, berobenatide (Pfizer) VESPER-1/2/3.
- Jun 6, 2026Retatrutide dysesthesia and UTI safety signal logged (up to ~21% dysesthesia at 12 mg in the TRIUMPH-4 obesity trial). Berobenatide promoted to phase 2 with Pfizer's once-monthly strategy.
The pipeline moves fast. I keep this current.
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