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BRAF V600E Mutation

3
Pipeline Programs
4
Companies
2
Clinical Trials
1 recruiting
0
Approved Products

Pipeline by Development Stage

Preclinical
Phase 1
Phase 1/2
Phase 2
Phase 2/3
Phase 3
On Market
0
1
0
2
0
0
0
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Small Molecule
2100%
+ 2 programs with unclassified modality

Competitive Landscape

4 companies ranked by most advanced pipeline stage

Genome & Company
Genome & CompanyKorea - Suwon
1 program
1
Dabrafenib MesylatePhase 2
Human BioSciences
Human BioSciencesWV - Martinsburg
1 program
1
Dabrafenib MesylatePhase 21 trial
Active Trials
NCT02281760Completed9Est. Aug 2018
BioTherapeutics Inc
BioTherapeutics IncVA - Blacksburg
1 program
1
PlixorafenibPhase 1Small Molecule1 trial
Active Trials
NCT06610682Recruiting24Est. Jun 2028
Fore Biotherapeutics
Fore BiotherapeuticsIsrael - Rehovot
1 program
PlixorafenibPHASE_1Small Molecule

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
2028
Human BioSciencesDabrafenib Mesylate
BioTherapeutics IncPlixorafenib

Clinical Trials (2)

Total enrollment: 33 patients across 2 trials

NCT02281760Human BioSciencesDabrafenib Mesylate

Dabrafenib and Trametinib in People With BRAF V600E Mutation Positive Lesions in Erdheim Chester Disease

Start: Nov 2014Est. completion: Aug 20189 patients
Phase 2Completed

A Trial to Evaluate CSF ctDNA and Safety of Plixorafenib Alone or With Retifanlimab in Patients With BRAF-altered Glioma

Start: Apr 2025Est. completion: Jun 202824 patients
Phase 1Recruiting

Phase Legend

PreclinicalLab & animal studies
Phase 1Safety & dosing
Phase 2Efficacy testing
Phase 3Large-scale trials
On MarketApproved & available

Key Insights

1 actively recruiting trials targeting 33 patients
Small Molecule is the dominant modality (100% of programs)
4 companies competing in this space

The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.