Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
duvelisib + BMS-986345 is an investigational combination therapy consisting of the dual PI3K-delta/gamma inhibitor duvelisib and the oral hypomethylating agent BMS-986345 (an oral formulation of azacitidine). This regimen is being evaluated in a Phase 1 clinical trial (NCT04635813) led by the H. Lee Moffitt Cancer Center and Research Institute for the treatment of relapsed or refractory lymphoid malignancies, including mature T-cell lymphomas. BMS-986345 functions as a DNA methyltransferase inhibitor that incorporates into DNA, leading to hypomethylation and the reactivation of tumor suppressor genes. Duvelisib complements this mechanism by inhibiting the delta and gamma isoforms of phosphoinositide 3-kinase (PI3K), which are critical for the signaling, proliferation, and survival of malignant lymphoid cells. The combination represents an all-oral approach to treating difficult-to-treat hematologic malignancies.
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 duvelisib + BMS-986345.