Roche Diabetes Drug Trial Met Primary End Points
A clinical trial showed enicepatide effectively reduced A1c levels and body weight in adults with type 2 diabetes.
Updated on Sept. 28, 2026 in Diabetes

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Roche announced that its experimental once-weekly treatment, enicepatide, successfully met primary end points in a 48-week phase 2 clinical trial. The study enrolled 447 adults living with type 2 diabetes and obesity to test the drug's efficacy and safety.
Why it matters
The positive results for enicepatide provide a potential new therapeutic option for the roughly 600 million adults globally who suffer from diabetes. By targeting both GLP-1 and GIP receptors, the drug aims to address both glycemic control and weight management in a single treatment.
In the phase 2 CT-388-104 trial, patients receiving the 24 mg dose achieved a 2.65% reduction in hemoglobin A1c and 15.5% mean weight loss. Only 2.0% of participants discontinued the study due to adverse events, which were primarily mild-to-moderate gastrointestinal effects.
The players
Roche
Roche is a global research-based healthcare company that develops pharmaceuticals and diagnostics.
The details
The trial utilized a multicenter, parallel-group design to evaluate subcutaneous enicepatide, a synthetic peptide that activates GLP-1 and GIP receptors while favoring cAMP signaling. The results establish a foundation for further investigation as the company moves toward later-stage development.
Timeline
The clinical trial treatment period lasted for 48 weeks.
Roche plans to initiate phase 3 glycemic control trials in the first half of 2027.
The Big Picture
This development follows a pattern of intense industry competition to expand the availability of dual-agonist weight loss and diabetes treatments within the GLP-1 and GIP receptor agonist therapeutic class.
While the drug is not yet approved for public use, these trial results indicate a future treatment path that could assist patients in managing both blood sugar levels and weight simultaneously. Individuals should consult their doctors for updates on medication availability and current standard-of-care options.
The takeaway
The successful trial results mark a significant step toward potential new treatments for complex metabolic conditions. Patients and healthcare providers should monitor future phase 3 results to better understand the long-term safety and efficacy of this synthetic peptide therapy.
What happens next
Roche has scheduled the initiation of both a phase 3 glycemic control program and cardiovascular outcomes trials for the first half of 2027.
Further reading
For more on the current landscape of metabolic disorder treatments, visit the Diabetes section.
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