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Completed Phase 1 Interventional

Phase 1/1b Study of MGCD516 in Patients With Advanced Cancer

ClinicalTrials.gov ID: NCT02219711

Public ClinicalTrials.gov record NCT02219711. 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 27, 2026, 12:11 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 Phase 1/1b Study of MGCD516 in Patients With Advanced Solid Tumor Malignancies

Brief summary

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

MGCD516 is a receptor tyrosine kinase (RTK) inhibitor shown in preclinical models to inhibit a closely related spectrum of RTKs including MET, AXL, MER, and members of the VEGFR, PDGFR, DDR2, TRK and Eph families. In this study, MGCD516 is orally administered to patients with advanced solid tumor malignancies to evaluate its safety, pharmacokinetic, metabolism, pharmacodynamic and clinical activity profiles. During the Phase 1 segment, the dose and regimen of MGCD516 will be assessed; during the Phase 1b segment, the clinical activity of MGCD516 will be evaluated in selected patient populations. Patients anticipated to be enrolled in Phase 1b will be selected based upon having a tumor type, including but not limited to, non small cell lung cancer and head and neck cancer positive for specific activating MET, NTRK2, NTRK3, or DDR2 mutations, MET or KIT/PDGFRA/KDR gene amplification, selected gene rearrangements involving the MET, RET, AXL, NTRK1, or NTRK3 gene loci, or having loss of function mutations in the CBL gene. In addition patients with clear cell renal cell carcinoma refractory to angiogenesis inhibitors or metastatic prostate cancer with bone metastasis will be enrolled.

Study identification

NCT ID
NCT02219711
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Mirati Therapeutics Inc.
Industry
Enrollment
193 participants

Conditions and interventions

Interventions

Drug

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
Aug 2014 (Type not available)
Primary completion
Apr 27, 2022 (Actual)
Completion
Apr 27, 2022 (Actual)
Last update posted
Mar 6, 2023

2014 – 2022

United States locations

U.S. sites
37
U.S. states
22
U.S. cities
36
Facility City State ZIP Site status
University of Alabama Birmingham Alabama 35294 —
University of California, San Diego San Diego California 92093 —
University of California, San Francisco San Francisco California 94143 —
Sarcoma Oncology Research Center Santa Monica California 90403 —
Innovative Clinical Research Institute Whittier California 90602 —
Rocky Mountain Cancer Center Denver Colorado 80218 —
Holy Cross Michael & Dianne Bienes Comprehensive Cancer Center Fort Lauderdale Florida 33308 —
Florida Cancer Affiliates Ocala Florida 34471 —
Florida Cancer Specialists Sarasota Florida 34232 —
Northwestern University Chicago Illinois 60611 —
Rush University Medical Center Chicago Illinois 60612 —
Ochsner Clinic Foundation New Orleans Louisiana 70121 —
Maryland Oncology Hematology, Rockville Maryland 20850 —
Massachusetts General Hospital Boston Massachusetts 02114 —
University of Michigan Ann Arbor Michigan 48109 —
Henry Ford Health System Detroit Michigan 48202 —
Washington University Center for Advanced Medicine St Louis Missouri 63110 —
CHI Health St Francis, Saint Francis Cancer Treatment Center Grand Island Nebraska 68803 —
Oncology Hematology West PC, Nebraska Cancer Specialists Omaha Nebraska 68130 —
University of New Mexico Cancer Research and Treatment Center Albuquerque New Mexico 87102 —
Roswell Park Cancer Institute Buffalo New York 14263 —
Columbia University New York New York 10032 —
Montefiore Medical Center The Bronx New York 10467 —
Oncology Hematology Care, Inc. Cincinnati Ohio 45242 —
Guthrie Clinical Research Sayre Pennsylvania 18840 —
St. Francis Cancer Center Greenville South Carolina 29607 —
Sarah Cannon Research Institute Nashville Tennessee 37203 —
Texas Oncology-Austin Midtown Austin Texas 78705 —
Mary Crowley Cancer Research Center Dallas Texas 75251 —
University of Texas, MD Anderson Cancer Center Houston Texas 77030 —
Texas Oncology-Tyler Tyler Texas 75702 —
The Huntsman Cancer Institute Salt Lake City Utah 84112 —
Virginia Cancer Specialists Fairfax Virginia 22031 —
Oncology and Hematology Associates of Southwest Virginia, Inc., Blue Ridge Cancer Care Roanoke Virginia 24014 —
Seattle Cancer Care Alliance Seattle Washington 98109 —
Northwest Cancer Specialists, P.C. Vancouver Washington 98684 —
University of Wisconsin Madison Wisconsin 53792 —

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 6 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02219711, 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 Mar 6, 2023 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02219711 live on ClinicalTrials.gov.

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