Comparative Effectiveness of Targeted Therapies in BRAF Positive Metastatic Melanoma in the US
Part of paid clinical trials in New York, New York.
- Sponsor
- Pfizer
- Study ID
- NCT05260684
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Encorafenib — DRUG450 mg QD
- Binimetinib — DRUG45 mg BID
- Vemurafenib — DRUG960 mg BID for 28 days/cycle
- Cobimetinib — DRUG60 mg QD for 21 days/cycle
- Dabrafenib — DRUG150 mg BID
- Trametinib — DRUG2 mg QD
Study Details
This study aims to compare real-world effectiveness of BRAF/MEK inhibitors in BRAF-mutant metastatic melanoma patients in the United States by line of therapy. The Flatiron Health electronic health record (EHR) data from US cancer clinics will be used for this retrospective database analysis.
Key Dates
- Start date
- Jan 17, 2022
- Status verified
- Mar 2025
- Primary completion
- Dec 31, 2023
- Completion
- Dec 31, 2023
Study Design
- Enrollment
- 716 participants (actual)
Arms
- Arm: Encorafenib + binimetinibEncorafenib 450 mg once a day (QD) Binimetinib 45 mg twice a day (BID)
- Arm: Vemurafenib + CobimetinibVemurafenib 960 mg twice a day (BID) for 28 days of 28 day cycle Cobimetinib 60 mg once a day (QD) for 21 days of 28 day cycle
- Arm: Dabrafenib + trametinibDabrafenib 150 mg twice a day (BID) Trametinib 2 mg once a day (QD)
Primary Outcome Measure
Overall Survival (OS) [ Time Frame: COLUMBUS: From date of randomization until death or censoring (approx 80.5 months); Flatiron: From index date until death due or censoring or end of follow-up period (92.7 months) ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Pfizer Investigational Site | New York | New York | 10017 | - |
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