Product Description
Mechanisms of Action: VEGFR2 Inhibitor,AhR Agonist
Novel Mechanism: No
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: Pfizer
Company Location: NEW YORK NY 10017
Company CEO: Albert Bourla
Additonal Commercial Interests: None
Clinical Description
Countries in Clinic:
Active Clinical Trial Count:
Highest Development Phases
Phase 3: Colorectal Cancer
Phase 2: Skin Cancer|Head and Neck Cancer|Sarcoma|Squamous Cell Carcinoma|Plasmacytoma|Melanoma|Kidney Cancer|Multiple Myeloma|Renal Cell Carcinoma|Preleukemia|Anemia, Aplastic|Myelodysplastic Syndrome|Chronic Myelomonocytic Leukemia|Acute Myeloid Leukemia|Chronic Myeloid Leukemia|Acute Myelomonocytic Leukemia|Acute Monocytic Leukemia|Anemia, Refractory, with Excess of Blasts|Juvenile Myelomonocytic Leukemia,|Sarcoma, Kaposi|Prostate Cancer|HIV Infections|Adenocarcinoma|Cervical Cancer|Brain Stem Cancer|Uterine Cancer|Glioma|Colorectal Cancer|Astrocytoma|Mesothelioma|Gastrointestinal Stromal Tumors
Phase 1: Inflammatory Breast Cancer|Brain Stem Cancer|Oncology Solid Tumor Unspecified|Fallopian Tube Cancer|Peritoneal Cancer|Ovarian Cancer|Sarcoma, Kaposi|Prostate Cancer|Vascular Cancer|Head and Neck Cancer
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
SUGEN-SU5416.031 | P3 |
Completed |
Colorectal Cancer |
2007-09-01 |
|
NCI-2012-02351 | P2 |
Completed |
Mesothelioma |
2007-02-01 |
|
NCI-2012-02345 | P2 |
Terminated |
Colorectal Cancer |
2007-02-01 |
|
U01CA062505 | P2 |
Completed |
Kidney Cancer|Renal Cell Carcinoma |
2007-02-01 |