Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
PE0116 + PE0105 is an investigational combination therapy being evaluated for the treatment of advanced solid tumors. The combination is currently in Phase 1b/2 clinical trials to assess its safety, tolerability, pharmacokinetics, and preliminary antitumor activity. The trial includes dose escalation and expansion phases to determine the maximum tolerated dose (MTD) and recommended phase 2 dose (RP2D). According to available information, both agents are administered as intravenous injections. At least one component of the combination (PE0116) is described as a recombinant human anti-PD-1 monoclonal antibody, suggesting an immunotherapy mechanism targeting immune checkpoint pathways. The developer of this drug combination is Shanghai HyaMab Biotechnology.
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 PE0116 + PE0105.