Fenretinide in Treating Patients With Metastatic or Unresectable Malignant Solid Tumors

PHASE1CompletedINTERVENTIONAL
Enrollment

21

Participants

Timeline

Start Date

November 30, 2006

Primary Completion Date

July 31, 2013

Conditions
Unspecified Adult Solid Tumor, Protocol Specific
Interventions
DRUG

fenretinide

4-HPR (Fenretinide) is given as a continuous intravenous infusion (CIV) for five consecutive days. Cycle is repeated every 3 weeks, if PR, CR or stable disease for 6 cycles.

OTHER

pharmacological study

samples drawn per protocol

Trial Locations (7)

79430

Texas Tech University Health Sciences Center, Lubbock

91105

City of Hope Medical Group, Pasadena

94553

Contra Costa Regional Medical Center, Martinez

95817

University of California Davis Cancer Center, Sacramento

91010-3000

City of Hope Comprehensive Cancer Center, Duarte

90027-0700

Childrens Hospital Los Angeles, Los Angeles

90089-9181

USC/Norris Comprehensive Cancer Center and Hospital, Los Angeles

All Listed Sponsors
collaborator

National Cancer Institute (NCI)

NIH

lead

California Cancer Consortium

NETWORK

NCT00387504 - Fenretinide in Treating Patients With Metastatic or Unresectable Malignant Solid Tumors | Biotech Hunter | Biotech Hunter