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BRAFTOVI + MEKTOVI

Therapy

BRAFTOVI (encorafenib) plus MEKTOVI (binimetinib), both from Pfizer, is a targeted regimen for tumors with specific BRAF pathway alterations.

Approvals
7
Indications
2
Biomarkers
1
Mapped tests
5

Where this therapy is approved with a companion diagnostic

Each row represents a defined combination of indication, biomarker criteria, and BRAFTOVI + MEKTOVI. Select a testing pathway to see the eligible companion diagnostic tests.

Indication-specific approvals

Approvals where BRAFTOVI + MEKTOVI is tied to a specific indication and biomarker definition.

IndicationBiomarker criteriaNotes
Melanoma
Solid Tumor · Melanoma
BRAF
  • V600E
View testing pathway →
Non-Small Cell Lung Cancer (NSCLC)
Solid Tumor · Lung
BRAF
  • V600E
View testing pathway →
Tumor-agnostic approvals

Approvals defined at the solid tumor level where biomarker criteria determine eligibility for BRAFTOVI + MEKTOVI.

No tumor-agnostic companion diagnostic approvals are currently mapped for this therapy.

Tests used in these approvals

These assays are identified in FDA labeling or sponsor materials as companion diagnostics or acceptable tests when considering BRAFTOVI + MEKTOVI for eligible patients.

Test
PGDx elio tissue complete CDx
Personal Genome Diagnostics, Inc. (Labcorp)
Method
NGS
Specimen
Tissue (FFPE)
Test
FoundationOne CDx
Foundation Medicine, Inc.
Method
NGS
Specimen
Tissue (FFPE)
Test
FoundationOne Liquid CDx
Foundation Medicine, Inc.
Method
NGS
Specimen
Whole blood
Test
MI Cancer Seek (MCS)
Caris Life Sciences
Method
NGS
Specimen
Tissue (FFPE)
Test
THXID BRAF Kit
bioMérieux Inc.
Method
PCR
Specimen
Tissue (FFPE)
This view is scoped to BRAFTOVI + MEKTOVI. You can also see how it compares with other therapies and indications on the main Know Your Companions™ map.
BRAFTOVI + MEKTOVI | CDxTests.com | CDx Tests