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Navitoclax

Alternative Names: navitoclax, abt-263
Latest Update: 2024-11-22
Latest Update Note: Clinical Trial Update

Product Description

Navitoclax is a BCL-XL/BCL-2 inhibitor that is being investigated to treat myelofibrosis. (Sourced from: https://www.abbvie.com/our-science/pipeline/navitoclax.html)

Mechanisms of Action: BCL2 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: AbbVie
Company Location: NORTH CHICAGO IL 60064
Company CEO: Richard A. Gonzalez
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Navitoclax

Countries in Clinic: Australia, Austria, Belgium, Bulgaria, Canada, Croatia, Czech Republic, Denmark, France, Germany, Greece, Hungary, Israel, Italy, Japan, Korea, Netherlands, New Zealand, Poland, Puerto Rico, Russia, Serbia, South Africa, Spain, Sweden, Switzerland, Taiwan, Turkey, Ukraine, United Kingdom, United States

Active Clinical Trial Count: 16

Highest Development Phases

Phase 3: Myelofibrosis

Phase 2: Acute Lymphoid Leukemia|Chronic Lymphoid Leukemia|Lymphocytic Chronic B-Cell Leukemia|Myelodysplastic Syndrome|Precursor Cell Lymphoblastic Leukemia-Lymphoma|Preleukemia

Phase 1: Acute Myeloid Leukemia|Myeloproliferative Disorders|Oncology Unspecified

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

TRANSFORM-2

P3

Active, not recruiting

Myelofibrosis

2031-11-25

TRANSFORM-1

P3

Unknown status

Myelofibrosis

2029-12-20

M16-109

P2

Unknown Status

Myelofibrosis

2029-03-08

2017-001398-17

P2

Unknown status

Myelofibrosis

2027-09-04

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