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: Uterine Cancer|Renal Cell Carcinoma|Sarcoma|Mesothelioma|Melanoma|Multiple Myeloma|Cervical Cancer|Colorectal Cancer|Prostate Cancer|Plasmacytoma|Gastrointestinal Stromal Tumors|HIV Infections|Sarcoma, Kaposi|Squamous Cell Carcinoma|Glioma|Astrocytoma|Kidney Cancer|Brain Stem Cancer|Skin Cancer|Head and Neck Cancer|Adenocarcinoma|Anemia, Refractory, with Excess of Blasts|Acute Monocytic Leukemia|Chronic Myeloid Leukemia|Chronic Myelomonocytic Leukemia|Acute Myelomonocytic Leukemia|Myelodysplastic Syndrome|Juvenile Myelomonocytic Leukemia,|Acute Myeloid Leukemia
Phase 1: Oncology Solid Tumor Unspecified|Ovarian Cancer|Sarcoma, Kaposi|Fallopian Tube Cancer|Peritoneal Cancer|Vascular Cancer|Brain Stem Cancer|Head and Neck Cancer|Prostate Cancer|Inflammatory Breast Cancer
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
SUGEN-SU5416.031 | P3 |
Completed |
Colorectal Cancer |
2007-09-01 |
|
NCI-2012-02345 | P2 |
Terminated |
Colorectal Cancer |
2007-02-01 |
|
U01CA062505 | P2 |
Completed |
Renal Cell Carcinoma|Kidney Cancer |
2007-02-01 |
|
NCI-2012-02351 | P2 |
Completed |
Mesothelioma |
2007-02-01 |