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Life sciences · Phase 3 Trial
ClinicalTrials.gov · October 13, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Phase 3 Trial.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
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Registry record from ClinicalTrials.gov (NCT07351058). This is a study registration, not published results. Lead sponsor: Hoffmann-La Roche. Recruitment status: RECRUITING. Phase: PHASE3. Study type: INTERVENTIONAL. Enrollment: 1600 participants (ESTIMATED). Conditions: Obesity or Overweight, Type 2 Diabetes Mellitus. Interventions: COMBINATION_PRODUCT: Placebo; COMBINATION_PRODUCT: Enicepatide. Primary outcome measures: Percent (%) Change from Baseline in Body Weight at Week 72 , Baseline through Week 72. Brief summary: The purpose of this study is to assess the efficacy and safety of enicepatide, a dual glucagon-like peptide-1 (GLP-1)/glucose-dependent insulinotropic polypeptide (GIP) receptor agonist (RA), at multiple doses compared with placebo for weight management in participants with obesity or overweight and Type 2 diabetes mellitus (T2DM).