Drugs / Enicepatide
last change 3 days ago re-read 3 minutes ago

Enicepatide

Developed for
obesity disorder · type 2 diabetes mellitus
Investigated by
Hoffmann-La Roche · Carmot Therapeutics, Inc. · Zealand Pharma

Trials 7

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 11 trial
Phase 1 NCT07626515 Jul 2026 → Apr 2027 expected — Hoffmann-La Roche Recruiting No outcome recorded
Phase 23 trials · 2 met primary
Phase 2 NCT07589686 Sep 2026 → Nov 2027 expected obesity disorder Hoffmann-La Roche Not yet recruiting No outcome recorded
Phase 2 NCT06628362 Nov 2024 → May 2026 overdue obesity disorder, type 2 diabetes mellitus Carmot Therapeutics, Inc. Active not recruiting Met primary
Phase 2 NCT06525935 Aug 2024 → Dec 2025 obesity disorder Carmot Therapeutics, Inc. Completed Met primary
Phase 33 trials
Phase 3 NCT07670416 Jul 2026 → Feb 2028 expected obesity disorder, type 2 diabetes mellitus Hoffmann-La Roche Recruiting No outcome recorded
Phase 3 NCT07351058 Mar 2026 → Aug 2028 expected obesity disorder, type 2 diabetes mellitus Hoffmann-La Roche Recruiting No outcome recorded
Phase 3 NCT07351045 Mar 2026 → Jul 2028 expected obesity disorder Hoffmann-La Roche Recruiting No outcome recorded

News releases announcing trial results or a regulatory action · 6

DateIssuerRelease
2026-06-01 Hoffmann-La Roche Results Roche to present new data advancing its obesity portfolio at the American Diabetes Association’s 2026 Scientific Sessions roche.com ↗
Late-breaking Phase II data highlight enicepatide’s (CT-388) efficacy and safety, reinforcing its potential to deliver best-in-class weight loss across a broad population of people living with overweight or obesity
2026-05-31 Genentech, Inc. Results Genentech to Present New Data Advancing Its Obesity Portfolio at the American Diabetes Association’s 2026 Scientific Sessions gene.com ↗
Late-breaking data from the Phase II (CT388-103) study will highlight clinical weight loss outcomes from investigational enicepatide in people living with overweight/obesity.
2026-01-27 Hoffmann-La Roche Results [Ad hoc announcement pursuant to Art. 53 LR] Roche announces positive Phase II results for its dual GLP-1/GIP receptor agonist CT-388 in people living with obesity roche.com ↗
The study found that once-weekly subcutaneous injections of CT-388 (titrated up to 24 mg) resulted in significant and clinically meaningful placebo-adjusted weight loss of 22.5% (efficacy estimand) without reaching a weight loss plateau at 48 weeks.
2026-01-26 Genentech, Inc. Results Genentech Announces Positive Phase II Results for Its Dual GLP-1/GIP Receptor Agonist CT-388 in People Living With Obesity gene.com ↗
2024-05-16 Hoffmann-La Roche Results [Ad hoc announcement pursuant to Art. 53 LR] Roche reports positive Phase Ib results for its dual GLP-1/GIP receptor agonist CT-388 in people with obesity roche.com ↗
Basel, 16 May 2024 - Roche (SIX: RO, ROG; OTCQX: RHHBY) announced today positive results from the Phase I clinical trial of CT-388, a dual GLP-1/GIP receptor agonist being developed for the treatment of obesity and type 2 diabetes.
2024-05-15 Genentech, Inc. Results Genentech Reports Positive Phase Ib Results for Its Dual GLP-1/GIP Receptor Agonist CT-388 in People With Obesity gene.com ↗

All press releases naming this drug 8 releases

DateIssuerRelease

Evidence & citations 3 cited values

Every value below carries the sentence it was read from. 7 sources stand behind the page.

FieldValueCited text
Known as Enicepatide ClinicalTrials.gov intervention name — accepted as the source's own label NCT06525935 ↗
6

NCT06628362 ↗

NCT07626515 ↗

NCT07351045 ↗

NCT07351058 ↗

NCT07589686 ↗

NCT07670416 ↗

Action Activate “dual glucagon like peptide-1 (GLP-1)/glucose-dependent insulinotropic polypeptide (GIP) receptor agonist (RA)” NCT07351045 ↗
Route Subcutaneous “Enicepatide will be administered subcutaneously (SC) once weekly at the randomized dosing regimen.” NCT06525935 ↗