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Clinical Trial
Clinical Trial Search
Trial Protocol ID USOR 23253: Select Solid Tumors
Trial Description
Clinical Study To Further Evaluate The Efficacy Of Dabrafenib Plus Trametinib In Patients With Rare BRAF V600E Mutation-Positive Unresectable or Metastatic Solid Tumors (Protocol v.00)
MOA: Dabrafenib is a RAF kinase inhibitor. Trametinib is an allosteric inhibitor of MEK1/2 and kinase activity.
Key Eligibility:
- Documented BRAF V600E mutation-positive solid tumor
- Study participants previously not treated with dabrafenib and/or trametinib (or other BRAF and/or MEK inhibitor(s)).
- Study participants who received dabrafenib and trametinib in the past for the treatment of other malignancies are eligible if treatment has been discontinued for >1 year
- Ability to provide scans for central imaging review
- Patients with NSCLC, melanoma, ATC, BTC, Glioma, and
CRC are excluded
Contact us regarding Clinical Trials at MOHRSCH@usoncology.com or call us at 877-664-7724
Disease Types
ClinicalTrials.gov NCT ID
- NCT05868629
