Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
BMS-986497 + azacitidine is an investigational combination therapy being evaluated for relapsed or refractory acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS)[3][5][7]. BMS-986497 is a **protein degrader** that selectively targets two proteins, **GSPT1** and **CD33**, on cancer cells. Its mechanism involves inducing the degradation of these proteins, thus impairing proliferation and survival of malignant cells[3][5]. Azacitidine is a **hypomethylating agent/chemotherapy** that interferes with the growth and spread of cancer cells by incorporating into DNA and RNA, leading to cytotoxicity and DNA hypomethylation[5]. The combination is currently under investigation in a Phase I trial to determine safety, tolerability, pharmacokinetics, and efficacy for patients who have failed alternative therapies[3][5][7]. Developed by Bristol Myers Squibb, this regimen is not yet FDA approved.
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 BMS-986497 + azacitidine.