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Completed Phase 1Phase 2 Interventional Results available

Uprosertib, Dabrafenib, and Trametinib in Treating Patients With Stage IIIC-IV Cancer

ClinicalTrials.gov ID: NCT01902173

Public ClinicalTrials.gov record NCT01902173. 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 Sep 11, 2026, 5:17 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 the Safety and Efficacy of the AKT Inhibitor GSK2141795 in Combination With Dabrafenib and Trametinib in Patients With BRAF Mutant Cancer

Brief summary

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

This phase I/II trial studies the side effects and the best dose of uprosertib when given together with dabrafenib and trametinib and to see how well they work in treating patients with stage IIIC-IV cancer. Uprosertib, dabrafenib, and trametinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving uprosertib with dabrafenib and trametinib may be a better treatment for cancer.

Study identification

NCT ID
NCT01902173
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Enrollment
27 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
Oct 7, 2013
Primary completion
May 15, 2018
Completion
Dec 22, 2023
Last update posted
Jan 13, 2025

2013 – 2023

United States locations

U.S. sites
16
U.S. states
6
U.S. cities
12
Facility City State ZIP Site status
USC / Norris Comprehensive Cancer Center Los Angeles California 90033
UCLA / Jonsson Comprehensive Cancer Center Los Angeles California 90095
California Pacific Medical Center-Pacific Campus San Francisco California 94115
UCSF Medical Center-Mount Zion San Francisco California 94115
UCHealth University of Colorado Hospital Aurora Colorado 80045
University of Michigan Comprehensive Cancer Center Ann Arbor Michigan 48109
Cleveland Clinic Foundation Cleveland Ohio 44195
Ohio State University Comprehensive Cancer Center Columbus Ohio 43210
Clackamas Radiation Oncology Center Clackamas Oregon 97015
Providence Milwaukie Hospital Milwaukie Oregon 97222
Providence Newberg Medical Center Newberg Oregon 97132
Providence Willamette Falls Medical Center Oregon City Oregon 97045
Providence Portland Medical Center Portland Oregon 97213
Providence Saint Vincent Medical Center Portland Oregon 97225
Oregon Health and Science University Portland Oregon 97239
PeaceHealth Southwest Medical Center Vancouver Washington 98664

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 NCT01902173, 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 Jan 13, 2025 · Synced Sep 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01902173 live on ClinicalTrials.gov.

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