ClinicalTrials.gov record
Terminated Phase 2 Interventional Results available

Study of Ulixertinib for Patients With Advanced Malignancies Harboring MEK or Atypical BRAF Alterations

ClinicalTrials.gov ID: NCT04488003

Public ClinicalTrials.gov record NCT04488003. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 16, 2026, 10:11 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Two-Part, Phase II, Multi-center Study of the ERK Inhibitor Ulixertinib (BVD-523) for Patients With Advanced Malignancies Harboring MEK or Atypical BRAF Alterations

Study identification

NCT ID
NCT04488003
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
BioMed Valley Discoveries, Inc
Industry
Enrollment
104 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 6, 2021
Primary completion
Feb 14, 2023
Completion
May 22, 2023
Last update posted
Jun 3, 2024

2021 – 2023

United States locations

U.S. sites
22
U.S. states
18
U.S. cities
22
Facility City State ZIP Site status
Mayo Clinic Phoenix Arizona 85054
Hoag Memorial Hospital Presbyterian Newport Beach California 92663
Christiana Care Health Services / Helen F. Graham Cancer Center Newark Delaware 19713
Johns Hopkins Sibley Memorial Hospital Washington D.C. District of Columbia 20016
University of Florida Gainesville Florida 32610
Mayo Clinic Jacksonville Florida 32224
Massachusetts General Hospital Boston Massachusetts 02114
Mayo Clinic Rochester Minnesota 55905
Metro-Minnesota Community Oncology Research Consortium (MMCORC) Saint Louis Park Minnesota 55416
Washington University School of Medicine - Siteman Cancer Center St Louis Missouri 63110
Columbia University Irving Medical Center New York New York 10032
Montefiore Medical Center The Bronx New York 10461
Duke University Medical Center / Duke Cancer Institute Durham North Carolina 27710
Kettering Cancer Center Kettering Ohio 45429
UPMC Hillman Cancer Center Pittsburgh Pennsylvania 15213
Avera Cancer Institute Sioux Falls South Dakota 57105
Tennessee Oncology, PLLC - Sarah Cannon (SCRI) Nashville Tennessee 37203
MD Anderson Cancer Center Houston Texas 77030
Virginia Cancer Specialists, PC Fairfax Virginia 22031
University of Washington/Seattle Cancer Care Alliance Seattle Washington 98109
University of Wisconsin Clinical Science Center Madison Wisconsin 53792
Marshfield Medical Center Marshfield Wisconsin 54449

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04488003, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 3, 2024 · Synced May 16, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04488003 live on ClinicalTrials.gov.

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