Study of RXDX-105, Potent RET Inhibitor in Patients With Advanced Lung Cancer and Other Solid Tumors

PHASE1CompletedINTERVENTIONAL
Enrollment

143

Participants

Timeline

Start Date

June 30, 2013

Primary Completion Date

December 31, 2018

Study Completion Date

February 28, 2019

Conditions
Solid Tumors
Interventions
DRUG

RXDX-105

"During Phase 1/1b, subjects will receive daily oral doses of RXDX-105 in 28-day cycles (except for Day 2 of Cycle 1). To determine the recommended Phase 2 dose (RP2D), doses will be administered in an escalated fashion starting at 20 mg/day.~During Phase 1b, subjects will be administered the RP2D in 28-day treatment cycles until documented radiographic progression, unacceptable toxicity, withdrawal of consent, or protocol specified parameters to stop treatment."

Trial Locations (14)

Unknown

City of Hope, Duarte

University of California Irvine College of Medicine, Irvine

University of California San Diego Moores Cancer Center, San Diego

Lombardi Comprehensive Cancer Center, Georgetown, Washington D.C.

Florida Cancer Center, Sarasota

University Cancer & Blood Center, LLC, Athens

Massachusetts General Hospital/Beth Israel Deaconess Med. Ctr./Dana Farber Cancer Institute, Boston

Henry Ford Health System, Detroit

Karmanos Cancer Center, Detroit

Washington University, St Louis

Memorial Sloan Kettering Cancer Center, New York

Fox Chase Cancer Center, Philadelphia

University of Texas MD Anderson Cancer Center, Houston

University of Washington, Seattle Cancer Care Alliance, Seattle

All Listed Sponsors
lead

Hoffmann-La Roche

INDUSTRY

NCT01877811 - Study of RXDX-105, Potent RET Inhibitor in Patients With Advanced Lung Cancer and Other Solid Tumors | Biotech Hunter | Biotech Hunter