Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**XP-3924** is an investigational, fixed-ratio **XeriSol** co-formulation of pramlintide and regular human insulin developed by Xeris for mealtime glycemic control in **type 1 diabetes mellitus**. It combines pramlintide, an amylin analog that slows gastric emptying, suppresses postprandial glucagon secretion, and promotes satiety, with insulin human, which activates the insulin receptor to lower blood glucose. In a completed randomized Phase 2 crossover study, a single subcutaneous pre-meal dose reduced post-challenge hyperglycemia relative to regular insulin alone while providing glycemic control comparable to separately injected pramlintide plus regular insulin.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on XP-3924.