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Valspodar

Alternative Names: valspodar, psc-833, psc833, psc 833
Latest Update: 2023-12-01
Latest Update Note: PubMed Publication

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

Map of Global Clinical Trials for Valspodar

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

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