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encorafenib + binimetinib (encorafenib-binimetinib)
This arm of the Strata PATH trial will assess the clinical benefit of Braftovi® (encorafenib) + Mekt
Encorafenib + binimetinib is a dual BRAF/MEK inhibitor combination approved for BRAF V600E/K mutant melanoma and other solid tumors. This fixed-dose regimen targets two sequential steps in the MAPK signaling pathway, providing enhanced efficacy and improved tolerability compared to monotherapy approaches.
At a glance
| Generic name | encorafenib-binimetinib |
|---|---|
| Sponsor | Pfizer Inc. |
| Drug class | This arm of the Strata PATH trial will assess the clinical benefit of Braftovi® (encorafenib) + Mekt |
| Therapeutic area | Oncology |
| Phase | discontinued |
Mechanism of action
Cancer cells often have mutations in the BRAF gene that cause them to grow uncontrollably. Encorafenib directly blocks the abnormal BRAF protein, cutting off one growth signal. However, cancer cells can sometimes bypass this by using a backup pathway involving another protein called MEK. Binimetinib blocks this MEK protein, preventing the cancer from escaping through that alternative route. By using both drugs together, the combination attacks the cancer cell's growth machinery from two angles simultaneously. This dual approach is more effective than using just one drug alone, because it reduces the cancer's ability to develop resistance. The drugs work on the same pathway but at different checkpoints, like closing two doors instead of one to prevent escape. This combination approach is particularly effective in melanomas and other cancers that carry specific BRAF mutations. The pairing also allows doctors to use lower doses of each drug while maintaining effectiveness, which often results in fewer side effects compared to higher doses of a single agent.
Approved indications
Pipeline indications
- Cancer — discontinued
Common side effects
Key clinical trials
- Study of Binimetinib With Encorafenib in Adults With Recurrent BRAF V600-Mutated HGG (Phase 2)
- The FLOTILLA Study: Providing Continued Access to The Study Medicines Encorafenib and Binimetinib fo (Phase 4)
- An Open-label Study of Encorafenib + Binimetinib in Patients With BRAFV600-mutant Non-small Cell Lun (Phase 2)
- A Clinical Trial of Three Study Medicines (Encorafenib, Binimetinib, and Pembrolizumab) in Patients (Phase 3)
- Pharmacokinetic Drug-drug Interaction Study of Encorafenib and Binimetinib on Probe Drugs in Patient (Phase 1)
- Study of Encorafenib + Cetuximab Plus or Minus Binimetinib vs. Irinotecan/Cetuximab or Infusional 5- (Phase 3)
- LGX818 and MEK162 in Combination With a Third Agent (BKM120, LEE011, BGJ398 or INC280) in Advanced B (Phase 2)
- Encorafenib, Binimetinib and Cetuximab in Subjects With Previously Untreated BRAF-mutant ColoRectal (Phase 2)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- encorafenib + binimetinib CI brief — competitive landscape report
- encorafenib + binimetinib updates RSS · CI watch RSS
- Pfizer Inc. portfolio CI