Product Description
Mechanisms of Action: CD20 Antagonist
Novel Mechanism: No
Modality: Antibody
Route of Administration: Intravenous
FDA Designation: None *
Approval Status: Not Approved
Approved Countries: None
Approved Indications: None
Known Adverse Events: None
Company: Gilead Sciences
Company Location: FOSTER CITY CA 94404
Company CEO: Daniel P. O’Day
Additonal Commercial Interests: None
Clinical Description
Countries in Clinic:
Active Clinical Trial Count:
Highest Development Phases
Phase 2: Lymphoma, Non-Hodgkin|Chronic Lymphoid Leukemia|Purpura, Thrombocytopenic, Idiopathic|Prolymphocytic Leukemia|Arthritis, Rheumatoid|Lymphoma, B-Cell|Lymphoma|Waldenstrom Macroglobulinemia|Prolymphocytic B-Cell Leukemia|Lymphocytic Chronic B-Cell Leukemia|Follicular Lymphoma|Diffuse Large B-Cell Lymphoma|Precursor Cell Lymphoblastic Leukemia-Lymphoma|Leukemia, Plasma Cell|Acute Lymphoid Leukemia
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
IM-T-hA20/90Y-hLL2-01 | P2 |
Withdrawn |
Lymphoma, Non-Hodgkin|Diffuse Large B-Cell Lymphoma |
2016-12-01 |
42% |
OSU-09024 | P2 |
Completed |
Lymphoma, B-Cell|Lymphoma, Non-Hodgkin |
2015-04-01 |
|
Monoclonal Antibodies In Recurrent B cell ALL (MARALL) | P2 |
Terminated |
Lymphoma |
2014-10-03 |
|
MARALL | P2 |
Unknown status |
Lymphoma, B-Cell|Precursor Cell Lymphoblastic Leukemia-Lymphoma|Acute Lymphoid Leukemia |
2014-08-01 |