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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

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

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
2028
Human BioSciencesDabrafenib Mesylate
Fore BiotherapeuticsPlixorafenib

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.