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Completed Phase 1 Interventional

Trametinib in Treating Patients With Advanced Cancer With or Without Hepatic Dysfunction

ClinicalTrials.gov ID: NCT02070549

Public ClinicalTrials.gov record NCT02070549. 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 23, 2026, 12:13 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

A Phase I Trial of Single Agent Trametinib (GSK1120212) in Advanced Cancer Patients With Hepatic Dysfunction

Brief summary

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

This phase I trial studies the side effects and best dose of trametinib in treating patients with cancer that has spread to other places in the body and usually cannot be cured or controlled with treatment (advanced) with or without liver (hepatic) dysfunction. Trametinib may stop the growth of tumor cells by blocking proteins needed for cell growth. When these proteins are blocked, the growth of cancer cells may be stopped and the cancer cells will then die. Hepatic dysfunction is frequently found in patients with advanced cancer and usually prevents patients from receiving standard treatments or from participating in clinical trials. Patients may also need dose adjustments or absorb drugs differently. Trametinib may be a better treatment for patients with advanced cancers and hepatic dysfunction.

Study identification

NCT ID
NCT02070549
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Enrollment
46 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 10, 2014 (Actual)
Primary completion
Dec 18, 2024 (Actual)
Completion
Dec 18, 2024 (Actual)
Last update posted
Feb 13, 2025

2014 – 2024

United States locations

U.S. sites
8
U.S. states
8
U.S. cities
8
Facility City State ZIP Site status
University of California Davis Comprehensive Cancer Center Sacramento California 95817 —
Moffitt Cancer Center Tampa Florida 33612 —
University of Chicago Comprehensive Cancer Center Chicago Illinois 60637 —
Wayne State University/Karmanos Cancer Institute Detroit Michigan 48201 —
Washington University School of Medicine St Louis Missouri 63110 —
Rutgers Cancer Institute of New Jersey New Brunswick New Jersey 08903 —
Ohio State University Comprehensive Cancer Center Columbus Ohio 43210 —
M D 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.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02070549, 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 Feb 13, 2025 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02070549 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →