Phase I Study of CBP501 and Cisplatin in Patients With Advanced Refractory Solid Tumors

PHASE1CompletedINTERVENTIONAL
Enrollment

48

Participants

Timeline

Start Date

November 30, 2006

Primary Completion Date

May 31, 2009

Study Completion Date

May 31, 2009

Conditions
CancerSolid Tumors
Interventions
DRUG

CBP501 and Cisplatin

CBP501 is given IV on Day 1 of each cycle (every 21 days). Dose escalation of CBP501 and cisplatin will be starting doses of 3.6 mg/m² CBP501 and 50 mg/m² cisplatin (Dose Level 1). Step 1, if during the first 2 cycles, at least 2 out of 3 to 6 patients experience Dose Limiting Toxicity (DLT) at 50 mg/m² cisplatin, then the cisplatin dose will be de-escalated to 30 mg/m². If no more than 1 out of 6 patients experiences DLT, cisplatin dose will be escalated to 75 mg/m². Step 2, dose escalation will be performed using the cisplatin MTD, with escalating CBP501 doses. CBP501 dose escalation will take place until the MTD has been defined or 74 mg/m² is reached.

Trial Locations (3)

85258

Scottsdale Clinical Research Institute, Scottsdale

89135

Nevada Cancer Institute, Las Vegas

02115

Dana Farber Cancer Institute, Boston

All Listed Sponsors
lead

CanBas Co. Ltd.

INDUSTRY

NCT00551512 - Phase I Study of CBP501 and Cisplatin in Patients With Advanced Refractory Solid Tumors | Biotech Hunter | Biotech Hunter