Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Glymera (froniglutide, code name PB1023) is a recombinant glucagon-like peptide-1 (GLP-1) analogue developed as a long-acting GLP-1 receptor agonist for the treatment of type 2 diabetes mellitus. It is designed to provide once-weekly subcutaneous dosing and aims to improve glycemic control by reducing fasting plasma glucose and hemoglobin A1c (HbA1c). The drug leverages PhaseBio’s ELP technology to control absorption rate and extend half-life, potentially resulting in improved gastrointestinal tolerability compared to other GLP-1 analogues. Clinical trials have demonstrated significant reductions in fasting glucose and average daily glucose with favorable safety and tolerability profiles. Glymera was investigated in phase 2b clinical trials for adults with type 2 diabetes inadequately controlled by diet, exercise, or oral antidiabetic agents[1][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 froniglutide.