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Buparlisib

Alternative Names: buparlisib, bkm120, bkm-120, bkm 120, AN2025, AN-2025, AN 2025
Latest Update: 2024-11-16
Latest Update Note: Clinical Trial Update

Product Description

An orally bioavailable specific oral inhibitor of the pan-class I phosphatidylinositol 3-kinase (PI3K) family of lipid kinases with potential antineoplastic activity. (Sourced from: https://www.cancer.gov/publications/dictionaries/cancer-drug/def/buparlisib)

Mechanisms of Action: PI3K Inhibitor

Novel Mechanism: No

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: Novartis
Company Location: BASEL V8 CH 4056
Company CEO: Vasant Narasimhan
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Buparlisib

Countries in Clinic: Argentina, Australia, Belgium, Canada, China, France, Germany, Hong Kong, Hungary, Italy, Japan, Korea, Poland, Spain, Taiwan, United Kingdom, United States, Unknown Location

Active Clinical Trial Count: 6

Highest Development Phases

Phase 3: Head and Neck Cancer|Squamous Cell Carcinoma

Phase 1: Diffuse Large B-Cell Lymphoma|Follicular Lymphoma|Mantle-Cell Lymphoma|Oncology Solid Tumor Unspecified

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

jRCT2011210034

P3

Recruiting

Squamous Cell Carcinoma|Head and Neck Cancer

2027-12-31

The BURAN Study

P3

Active, not recruiting

Head and Neck Cancer|Squamous Cell Carcinoma

2026-12-14

BURAN

P3

Active, not recruiting

Head and Neck Cancer

2025-06-30

35%

AN2025H0301

P3

Unknown Status

Squamous Cell Carcinoma|Head and Neck Cancer

2025-04-25

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