ERK inhibitor · small molecule
ulixertinib
2 active trials across 4 of our biomarkers, targeting ERK1/2. Not approved for any biomarker on marked.bio yet.
Also known as BVD-523.
Counts only trials that select patients by one of the biomarkers on marked.bio, not every trial of this drug.
Biomarkers
| Biomarker | Active trials | All trials | Furthest active phase |
|---|---|---|---|
| BRAF V600E | 2 | 4 | Phase 2 |
| KRAS G12C | 0 | 1 | – |
| KRAS G12D | 0 | 1 | – |
| MSI-H / dMMR | 0 | 1 | – |
Trials
2 of 6 trials shown
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Ulixertinib in People With Histiocytic Neoplasms
Concordance between cfDNA and tumor sequencing for BRAFV600E and non-BRAF mutations in histiocytic neoplasms has been documented by our group and othe…
BRAF V600EHistiocytic Neoplasms
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Open-label Phase 1b Study of Ulixertinib and Cetuximab or Ulixertinib in Combination With Cetuximab and Encorafenib in Patients With Unresectable or Metastatic Colorectal Cancer Who Have Previously Received EGFR or BRAF-directed Therapy
cetuximab FDA EUulixertinibencorafenib FDA EU
BRAF expansion Cohort: BRAF V600E mutation must be present
BRAF V600EMetastatic Colorectal Cancer
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Trial of Ulixertinib in Combination With Hydroxychloroquine in Patients With Advanced Gastrointestinal (GI) Malignancies
ulixertinibhydroxychloroquine
Patients with deficient MisMatch Repair/High levels of MicroSatellite Instability (dMMR/MSI-H) tumors must have progressed during or after pembrolizumab.
MSI-H / dMMRTumor, Solid, Gastrointestinal Cancer
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Study of Ulixertinib for Patients With Advanced Malignancies Harboring MEK or Atypical BRAF Alterations
ulixertinibPhysician's Choice
Tumors harboring a MEK or atypical BRAF alteration.
BRAF V600EAdvanced Solid Tumor, BRAF Gene Mutation, BRAF Gene Alteration, MEK Mutation
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Phase 1/2 Study of the ERK1/2 Inhibitor BVD-523 in Patients With Acute Myelogenous Leukemia or Myelodysplastic Syndromes
Positive for RAS mutation at a Clinical Laboratory Improvement Amendments (CLIA)-certified laboratory prior to stud…
KRAS G12CKRAS G12DAcute Myelogenous Leukemia, Myelodysplastic Syndrome
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Phase I Dose-Escalation, Safety, Pharmacokinetic and Pharmacodynamic Study of BVD-523 in Patients With Advanced Malignancies
Group 1: Patients with BRAF mutated cancer, except those with colorectal or non-small cell lung cancers
BRAF V600EAdvanced Solid Tumors
No trials match these filters.