Product

Vemurafenib

Aliases
BRAF (V600E) kinase inhibitor RO5185426, BRAF(V600E) Kinase Inhibitor RO5185426, PLX4032, PLX-4032, RG7204 (9 other aliases)
Name
ZELBORAF
FDA Approved
Yes

39 clinical trials

1 organization

1 drug

106 indications

1 document

Indication
Melanoma
Indication
Cancer
Indication
Solid Tumors
Indication
Salivary Cancer
Indication
Bladder Cancer
Indication
Lung Cancer
Indication
Solid Tumor
Indication
Ependymoma
Indication
Ewing Sarcoma
Indication
Hepatoblastoma
Indication
Medulloblastoma
Indication
Neuroblastoma
Indication
Osteosarcoma
Indication
Glioma
Indication
Rhabdoid Tumor
Indication
Wilms tumor
Indication
Skin Cancer
Indication
Breast Cancer
Indication
Ovarian Cancer
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Prostate Cancer
Indication
Thyroid Cancer
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Advanced Cancer
Indication
Leukemia
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Hairy Cell
Indication
BRAF
Indication
Neoplasm
Indication
Histiocytosis
Indication
Papillary
Indication
cancer
Indication
Anaplastic
Indication
Follicular
Indication
hepatoblastoma
Indication
Germ Cell Tumor
Indication
NSCLC
Clinical trial
NCI-COG Pediatric MATCH (Molecular Analysis for Therapy Choice) Screening Protocol
Status: Recruiting, Estimated PCD: 2027-09-30
Clinical trial
The Rome Trial From Histology to Target: the Road to Personalize Target Therapy and Immunotherapy
Status: Active (not recruiting), Estimated PCD: 2024-12-01
Clinical trial
Deciphering Antitumour Response and Resistance With INtratumour Heterogeneity - DARWINII
Status: Active (not recruiting), Estimated PCD: 2026-05-01
Clinical trial
Phase II Trial of BRAF/MEK Inhibitors in Papillary Craniopharyngiomas
Status: Active (not recruiting), Estimated PCD: 2024-10-01
Clinical trial
Atezolizumab Combinations With Chemotherapy for Anaplastic and Poorly Differentiated Thyroid Carcinomas
Status: Active (not recruiting), Estimated PCD: 2025-07-31
Clinical trial
Secured Access to Vemurafenib for Patients With Tumors Harboring BRAF Genomic Alterations
Status: Active (not recruiting), Estimated PCD: 2019-05-07
Organization
Genentech, Inc.