Phase I/II study of dabrafenib, trametinib, and navitoclax in BRAF mutant melanoma (Phase I and II) and other solid tumors (Phase I only)
Sponsor: |
National Cancer Institute NCI |
Enrolling: |
Male and Female Patients |
IRB Number: |
AAAS2517 |
U.S. Govt. ID: |
NCT01989585 |
Contact: |
Research Nurse Navigator: 212-342-5162 / cancerclinicaltrials@cumc.columbia.edu |
The purpose of the first part (Phase I) of the study is to test the safety of navitoclax in combination with dabrafenib and trametinibat different doses to find out what effects, if any, it has on people. There will be about 18 people treated in this part of the study. The purpose of the second part of this study (Phase II) is to compare the good and bad effects of navitoclax in combination with dabrafenib and trametinib to using the usual approach of dabrafenib and trametinib in patients with BRAF-mutant melanoma. This study will allow the researchers to know whether this different approach is better, the same, or worse than the usual approach. There will be 50 people taking part in this part of the study.
This study is closed
Investigator
Richard Carvajal, MD
Are you 18 years of age or older? |
Yes |
No |
Do you have a BRAF-mutant melanoma that has spread or is unresectable? |
Yes |
No |
Are you able to carry out light work (e.g. light house work or office work)? |
Yes |
No |