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Mivebresib

Alternative Names: mivebresib, abbv-075
Latest Update: 2024-05-15
Latest Update Note: PubMed Publication

Product Description

Mivebresib is an inhibitor of the Bromodomain and Extra-Terminal (BET) family of proteins, with potential antineoplastic activity. Upon administration, mivebresib binds to the acetyl-lysine binding site of BRD-containing protein(s), thereby preventing the interaction between those proteins and acetylated histones. This disrupts chromatin remodeling, prevents the expression of certain growth-promoting genes, and leads to an inhibition of cell growth in susceptible tumors. (Sourced from: https://pubchem.ncbi.nlm.nih.gov/compound/Mivebresib)

Mechanisms of Action: BET Inhibitor

Novel Mechanism: Yes

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: AbbVie
Company Location: NORTH CHICAGO IL 60064
Company CEO: Richard A. Gonzalez
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 1: Breast Cancer|Lymphoma, Non-Hodgkin|Non-Small-Cell Lung Cancer|Prostate Cancer|Acute Myeloid Leukemia|Multiple Myeloma|Myelofibrosis

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

M20-248

P1

Terminated

Myelofibrosis

2023-07-28

21%

M14-546

P1

Completed

Acute Myeloid Leukemia|Lymphoma, Non-Hodgkin|Non-Small-Cell Lung Cancer|Multiple Myeloma|Prostate Cancer|Breast Cancer

2019-07-05

32%

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