Study of GO-203-2C Given Intravenously in Patients With Advanced Solid Tumors Including Lymphomas

PHASE1CompletedINTERVENTIONAL
Enrollment

23

Participants

Timeline

Start Date

January 31, 2011

Primary Completion Date

May 31, 2013

Study Completion Date

May 31, 2013

Conditions
Solid Tumors
Interventions
DRUG

GO-203-2c

GO-203-2c Injection is a non-preserved, sterile, ready-to-use liquid dosage form provided in a glass vial with rubber closure and crimp seal. Injection will be added to the contents of an intravenous bag (of 0.9% NS, D5W or sterile water) to a final concentration of between 0.03 - 0.3 mg/ml (preferable in 100 mls or greater) and administered as a single agent intravenously over 60 minutes. A treatment cycle will consist of a daily IV dose administered for 21 consecutive days followed by a 7 day rest.

Trial Locations (4)

78229

University of Texas Health Science Center San Antonio, San Antonio

85258

TGen Clinical Research Service, Scottsdale

90048

Cedars-Sinai Medical Center, Los Angeles

02215

Beth Israel Deaconess Medical Center, Boston

Sponsors
All Listed Sponsors
lead

Genus Oncology, LLC

INDUSTRY