Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
PE0139 is a novel, super-long-acting basal insulin designed for the treatment of hyperglycemia associated with diabetes, particularly type 2 diabetes mellitus. It consists of a fully mature, native insulin molecule genetically fused to an elastin-like polypeptide (ELP) biopolymer using recombinant technology. This fusion extends the half-life of insulin, enabling once-weekly subcutaneous dosing by providing prolonged exposure and a flat pharmacokinetic profile with low peak-to-trough ratio. In clinical studies, PE0139 demonstrated dose-related reductions in fasting plasma glucose and was well tolerated without serious adverse events or hypoglycemia. Nonclinical models showed that PE0139 provided longer blood glucose reduction than standard basal insulins like insulin glargine and exhibited synergistic effects when combined with GLP-1 receptor agonists such as PB1023. The drug was developed by PhaseBio Pharmaceuticals but its development for type 2 diabetes mellitus was discontinued after phase II trials[1][2][4][5][7].
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 pe0139.