Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Mivebresib (ABBV-075) is an orally bioavailable, small-molecule pan-inhibitor of the bromodomain and extra-terminal (BET) family of proteins, including BRD2, BRD4, and BRDT. Developed by AbbVie, it functions as an epigenetic modulator by binding to the bromodomains of BET proteins, which are "readers" of acetylated lysine residues on histone tails. By preventing BET proteins from binding to chromatin, mivebresib inhibits the transcription of key oncogenic drivers such as MYC. It has been investigated in Phase 1 clinical trials for the treatment of advanced solid tumors (including breast, prostate, and lung cancers) and hematologic malignancies (such as acute myeloid leukemia and multiple myeloma), both as a monotherapy and in combination with other agents like venetoclax.
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 mivebresib (AbbVie Inc.).