Clinical Trial

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