Dabrafenib and/or Trametinib Rollover Study

This study is to provide access for patients who are receiving treatment with dabrafenib and/or trametinib in a Novartis-sponsored Oncology Global Development, Global Medical Affairs or a former GSK-sponsored study who have fulfilled the requirements for the primary objective, and who are judged by the investigator as benefiting from continued treatment in the parent study as judged by the Investigator at the completion of the parent study.

Trial Details

NCT ID
NCT03340506
Phase
PHASE4
Sponsor
Novartis Pharmaceuticals
Status
RECRUITING
Cancer Type
Non-Small Cell (NSCLC) Lung Cancer
Interventions
  • dabrafenib
  • trametinib
Locations (sample)
  • Scottsdale, Arizona, United States|33.50921,-111.89903
  • Scottsdale, Arizona, United States|33.50921,-111.89903
  • Bethesda, Maryland, United States|38.98067,-77.10026
  • Columbus, Ohio, United States|39.96118,-82.99879
  • Dallas, Texas, United States|32.78306,-96.80667

Key Eligibility Criteria

  • Patient is currently receiving treatment with dabrafenib/trametinib monotherapy or combination within a Novartis or former GSK sponsored study whic…
  • In the opinion of the Investigator would benefit from continued treatment.

For full eligibility, visit ClinicalTrials.gov.

Check If You May Be Eligible

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