Product Description
Mechanisms of Action: PK Inhibitor,TK Inhibitor,JAK2 Inhibitor,FLT3 Inhibitor
Novel Mechanism: Yes
Modality: Small Molecule
Route of Administration: Oral,Topical
FDA Designation: None *
Approval Status: Not Approved
Approved Countries: None
Approved Indications: None
Known Adverse Events: None
Company: Teva
Company Location: PETACH TIKVA L3 49131
Company CEO: Kåre Schultz
Additonal Commercial Interests: None
Clinical Description
Countries in Clinic:
Active Clinical Trial Count:
Highest Development Phases
Phase 3: T-Cell Leukemia|Precursor T-Cell Lymphoblastic Leukemia-Lymphoma|Acute Lymphoid Leukemia|Precursor Cell Lymphoblastic Leukemia-Lymphoma
Phase 2: Myelofibrosis|Acute Myeloid Leukemia|Thrombocytosis|Thrombocythemia, Essential|Multiple Myeloma|Psoriasis|Polycythemia Vera|Prostate Cancer|Leukemia|Oncology Hematological Unspecified
Phase 1: Neuroblastoma
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
2006-7041-83/hah | N/A |
Not yet recruiting |
Multiple Sclerosis |
2018-07-01 |
|
AALL0631 | P3 |
Completed |
Acute Lymphoid Leukemia|T-Cell Leukemia|Precursor Cell Lymphoblastic Leukemia-Lymphoma|Precursor T-Cell Lymphoblastic Leukemia-Lymphoma |
2017-09-30 |
|
GCO 07-0548-00104 | P2 |
Unknown status |
Polycythemia Vera|Thrombocytosis|Thrombocythemia, Essential|Myelofibrosis |
2013-09-01 |
|
CS-2007-20040 | P2 |
Completed |
Myelofibrosis|Leukemia |
2010-05-01 |