Product Description
Mechanisms of Action: P-gp Inhibitor
Novel Mechanism: No
Modality: Large Molecule
Route of Administration: Intravenous
FDA Designation: None *
Approval Status: Not Approved
Approved Countries: None
Approved Indications: None
Known Adverse Events: None
Company: National Cancer Institute (NCI)
Company Location:
Company CEO:
Additonal Commercial Interests: None
Clinical Description
Countries in Clinic:
Active Clinical Trial Count:
Highest Development Phases
Phase 3: Acute Eosinophilic Leukemia|Acute Erythroblastic Leukemia|Acute Myeloid Leukemia|Plasmacytoma|Multiple Myeloma|Acute Monocytic Leukemia|Acute Megakaryoblastic Leukemia|Acute Myelomonocytic Leukemia|Myelodysplastic Syndrome|Hypereosinophilic Syndrome|Acute Basophilic Leukemia|Chronic Myeloid Leukemia|Preleukemia|Chronic Myelomonocytic Leukemia
Phase 2: Breast Cancer|Leukemia|Acute Myeloid Leukemia
Phase 1: Renal Cell Carcinoma|Lymphoma|Leukemia|Breast Cancer|Ovarian Cancer|Sarcoma, Kaposi|Kidney Cancer
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
NCI-2012-01835 | P1 |
Completed |
Leukemia |
2006-03-01 |
|
NCI-2012-02824 | P3 |
Completed |
Chronic Myelomonocytic Leukemia|Acute Basophilic Leukemia|Hypereosinophilic Syndrome|Acute Myeloid Leukemia|Myelodysplastic Syndrome|Acute Megakaryoblastic Leukemia|Acute Eosinophilic Leukemia|Acute Erythroblastic Leukemia|Preleukemia|Chronic Myeloid Leukemia|Acute Myelomonocytic Leukemia|Acute Monocytic Leukemia |
2005-06-01 |
|
CDR0000065011 | P2 |
Completed |
Breast Cancer |
2003-11-01 |
|
CDR0000065333 | P2 |
Completed |
Leukemia |
2003-11-01 |