Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
CBX129801 is a pegylated form of synthetic human C-peptide developed to extend the half-life of native C-peptide in circulation. It was investigated as a replacement therapy for patients with type 1 diabetes, particularly targeting diabetic peripheral neuropathy, a common complication in this population. The drug is administered subcutaneously and aims to restore physiological levels of circulating C-peptide. Mechanistically, it acts as an adenosine triphosphatase stimulant, nerve growth factor stimulant, and nitric oxide synthase stimulant—mechanisms believed to support nerve function and repair. Clinical development reached phase 2 trials for type 1 diabetes and diabetic neuropathies but has since been discontinued[2][3][4][5][6].
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 Pegylated synthetic human C-peptide.