Safety Study of Oral MGCD265 Administered Without Interruption to Subjects With Advanced Malignancies

PHASE1CompletedINTERVENTIONAL
Enrollment

180

Participants

Timeline

Start Date

June 30, 2008

Primary Completion Date

September 30, 2018

Study Completion Date

January 31, 2019

Conditions
Advanced Cancer
Interventions
DRUG

MGCD265

Oral daily administration without interruption

Trial Locations (19)

10032

Columbia University, Herbert Irving Comprehensive Cancer Center, New York

19111

Fox Chase Cancer Center, Philadelphia

27710

Duke University Medical Center, Durham

60637

University of Chicago, Chicago

63110

Washington University, Alvin J. Siteman Cancer Center, St Louis

77030

University of Texas, MD Anderson Cancer Center, Houston

84112

Huntsman Cancer Institute, Salt Lake City

91010

City of Hope, Duarte

92093

UC San Diego, San Diego

92868

UC Irvine Medical Center, Orange

98109

Seattle Cancer Care Alliance, Seattle

02115

Dana-Farber Cancer Institute, Boston

T6G 1Z2

Cross Cancer Institute, Edmonton

V5Z 4E6

British Columbia Cancer Agency, Vancouver Center, Vancouver

H3T IE2

Jewish General Hospital, Montreal

410-769

National Cancer Center, Gyeonggi-do

110-744

Seoul National University Hosptial, Seoul

135-710

Samsung Medical Center, Seoul

Unknown

Yonsei University Health System, Severance Hospital, Seoul

Sponsors
All Listed Sponsors
lead

Mirati Therapeutics Inc.

INDUSTRY

NCT00697632 - Safety Study of Oral MGCD265 Administered Without Interruption to Subjects With Advanced Malignancies | Biotech Hunter | Biotech Hunter