Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Combination of **nivolumab** (a monoclonal antibody immune checkpoint inhibitor targeting PD-1) and an **IDO1 inhibitor** (commonly BMS-986205, a small molecule orally administered inhibitor of indoleamine 2,3-dioxygenase 1). The rationale for the combination is that IDO1 orchestrates immune suppression and contributes to resistance against immune checkpoint inhibitors. The dual inhibition aims to overcome tumor immune escape by blocking both the suppressive effects of PD-1/PD-L1 signaling and tryptophan metabolism via IDO1. This combination has been investigated in several phase I/II clinical trials across tumor types including hepatocellular carcinoma, endometrial cancer, melanoma, and glioblastoma, with mechanistic synergy observed preclinically and some clinical evidence of enhanced antitumor activity and tolerable safety profiles[1][3][4][5].
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 nivolumab + IDO1 inhibitor.