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
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 |