Product Description
Mechanisms of Action: CDK9 Inhibitor
Novel Mechanism: Yes
Modality: Small Molecule
Route of Administration: Intravenous
FDA Designation: None *
Approval Status: Not Approved
Approved Countries: None
Approved Indications: None
Known Adverse Events: None
Company: Merck
Company Location: KENILWORTH NJ 07033
Company CEO: Robert M. Davis
Additonal Commercial Interests: None
Clinical Description
Countries in Clinic:
Active Clinical Trial Count:
Highest Development Phases
Phase 3: Chronic Lymphoid Leukemia|Lymphocytic Chronic B-Cell Leukemia
Phase 2: Non-Small-Cell Lung Cancer|Acute Lymphoid Leukemia|Precursor Cell Lymphoblastic Leukemia-Lymphoma|Acute Myeloid Leukemia|Prolymphocytic B-Cell Leukemia|Breast Cancer|Melanoma|Chronic Lymphoid Leukemia|Lymphocytic Chronic B-Cell Leukemia|Prolymphocytic Leukemia|Lymphoma, B-Cell|Multiple Myeloma|Mantle-Cell Lymphoma|Lentigo|Hutchinson's Melanotic Freckle
Phase 1: Pancreatic Cancer|Multiple Myeloma|Acute Myeloid Leukemia|Adenocarcinoma|Lymphoma, B-Cell|Lymphocytic Chronic B-Cell Leukemia|Chronic Lymphoid Leukemia|Lymphoma, Non-Hodgkin|Triple Negative Breast Cancer|Diffuse Large B-Cell Lymphoma|Male Breast Cancer
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
M16-183 | P1 |
Terminated |
Acute Myeloid Leukemia |
2022-12-01 |
28% |
NCI-2018-01053 | P1 |
Completed |
Triple Negative Breast Cancer |
2020-06-30 |
|
KEYNOTE-155 | P1 |
Terminated |
Chronic Lymphoid Leukemia|Diffuse Large B-Cell Lymphoma |
2020-04-06 |
|
NCI-2012-01737 | P1 |
Completed |
Multiple Myeloma |
2016-11-22 |