Product Description
Mechanisms of Action: TGFR Inhibitor
Novel Mechanism: No
Modality: Fusion Protein
Route of Administration: Oral,Subcutaneous
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 2: Squamous Cell Carcinoma|Mucinous Cystadenocarcinoma|Serous Cystadenocarcinoma|Mucinous Adenocarcinoma|Transitional Cell Carcinoma|Clear Cell Adenocarcinoma|Endometrial Cancer|Renal Cell Carcinoma|Ovarian Cancer|Head and Neck Cancer|Hepatocellular Carcinoma
Phase 1: Multiple Myeloma
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
A041-05 | P2 |
Completed |
Hepatocellular Carcinoma |
2017-07-05 |
|
A041-04 | P2 |
Terminated |
Renal Cell Carcinoma |
2017-06-01 |
|
GOG-0229N | P2 |
Completed |
Serous Cystadenocarcinoma|Endometrial Cancer|Clear Cell Adenocarcinoma|Mucinous Cystadenocarcinoma|Transitional Cell Carcinoma|Squamous Cell Carcinoma|Mucinous Adenocarcinoma |
2016-01-01 |
|
GOG-0170R | P2 |
Completed |
Ovarian Cancer |
2015-10-31 |