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Active, not recruiting Phase 1Phase 2 Interventional

Testing the Addition of Navitoclax to the Combination of Dabrafenib and Trametinib in People Who Have BRAF Mutant Melanoma

ClinicalTrials.gov ID: NCT01989585

Public ClinicalTrials.gov record NCT01989585. 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 Oct 17, 2026, 12:19 PM EDT

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

Official title

Phase I/II Study of Dabrafenib, Trametinib, and Navitoclax in BRAF Mutant Melanoma (Phase I and II) and Other Solid Tumors (Phase I Only)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This phase I/II trial studies the side effects and best dose of dabrafenib, trametinib, and navitoclax and to see how well they work in treating patients with BRAF mutant melanoma or solid tumors that has spread from where it first started (primary site) to other places in the body (metastatic) or cannot be removed by surgery (unresectable). Dabrafenib and trametinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Navitoclax is in a class of medications called B-cell lymphoma-2 (BCL-2) inhibitors. It may stop the growth of tumor cells by blocking Bcl-2, a protein needed for tumor cell survival. Giving navitoclax, dabrafenib, and trametinib may help shrink tumors in patients with melanoma.

Study identification

NCT ID
NCT01989585
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 1, Phase 2
Enrollment
75 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
Mar 24, 2014 (Actual)
Primary completion
Dec 31, 2027 (Estimated)
Completion
Dec 31, 2027 (Estimated)
Last update posted
Aug 11, 2026

2014 – 2027

United States locations

U.S. sites
49
U.S. states
16
U.S. cities
40
Facility City State ZIP Site status
Mayo Clinic Hospital in Arizona Phoenix Arizona 85054 —
Mayo Clinic in Arizona Scottsdale Arizona 85259 —
Los Angeles General Medical Center Los Angeles California 90033 —
USC / Norris Comprehensive Cancer Center Los Angeles California 90033 —
USC Norris Oncology/Hematology-Newport Beach Newport Beach California 92663 —
UC Irvine Health/Chao Family Comprehensive Cancer Center Orange California 92868 —
University of California Davis Comprehensive Cancer Center Sacramento California 95817 —
UCHealth University of Colorado Hospital Aurora Colorado 80045 —
UM Sylvester Comprehensive Cancer Center at Aventura Aventura Florida 33180 —
UM Sylvester Comprehensive Cancer Center at Coral Gables Coral Gables Florida 33146 —
UM Sylvester Comprehensive Cancer Center at Deerfield Beach Deerfield Beach Florida 33442 —
University of Miami Miller School of Medicine-Sylvester Cancer Center Miami Florida 33136 —
UM Sylvester Comprehensive Cancer Center at Kendall Miami Florida 33176 —
UM Sylvester Comprehensive Cancer Center at Plantation Plantation Florida 33324 —
Moffitt Cancer Center - McKinley Campus Tampa Florida 33612 —
Moffitt Cancer Center Tampa Florida 33612 —
Northwestern University Chicago Illinois 60611 —
University of Iowa/Holden Comprehensive Cancer Center Iowa City Iowa 52242 —
University of Kansas Clinical Research Center Fairway Kansas 66205 —
HaysMed Hays Kansas 67601 —
University of Kansas Cancer Center Kansas City Kansas 66160 —
Lawrence Memorial Hospital Lawrence Kansas 66044 —
The University of Kansas Cancer Center - Olathe Olathe Kansas 66061 —
University of Kansas Cancer Center-Overland Park Overland Park Kansas 66210 —
University of Kansas Hospital-Indian Creek Campus Overland Park Kansas 66211 —
Mercy Hospital Pittsburg Pittsburg Kansas 66762 —
Salina Regional Health Center Salina Kansas 67401 —
University of Kansas Health System Saint Francis Campus Topeka Kansas 66606 —
University of Kansas Hospital-Westwood Cancer Center Westwood Kansas 66205 —
Massachusetts General Hospital Cancer Center Boston Massachusetts 02114 —
Dana-Farber Cancer Institute Boston Massachusetts 02215 —
Mayo Clinic in Rochester Rochester Minnesota 55905 —
Siteman Cancer Center at Saint Peters Hospital City of Saint Peters Missouri 63376 —
Siteman Cancer Center at West County Hospital Creve Coeur Missouri 63141 —
University Health Truman Medical Center Kansas City Missouri 64108 —
University of Kansas Cancer Center - North Kansas City Missouri 64154 —
University of Kansas Cancer Center - Lee's Summit Lee's Summit Missouri 64064 —
University of Kansas Cancer Center at North Kansas City Hospital North Kansas City Missouri 64116 —
Washington University School of Medicine St Louis Missouri 63110 —
Siteman Cancer Center-South County St Louis Missouri 63129 —
Siteman Cancer Center at Christian Hospital St Louis Missouri 63136 —
Rutgers Cancer Institute of New Jersey New Brunswick New Jersey 08903 —
Laura and Isaac Perlmutter Cancer Center at NYU Langone New York New York 10016 —
NYP/Columbia University Medical Center/Herbert Irving Comprehensive Cancer Center New York New York 10032 —
UNC Lineberger Comprehensive Cancer Center Chapel Hill North Carolina 27599 —
Duke University Medical Center Durham North Carolina 27710 —
Ohio State University Comprehensive Cancer Center Columbus Ohio 43210 —
Thomas Jefferson University Hospital Philadelphia Pennsylvania 19107 —
UT MD Anderson Cancer Center Houston Texas 77030 —

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 NCT01989585, 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 Aug 11, 2026 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01989585 live on ClinicalTrials.gov.

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