drugset / Trial / NCT00551512

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

NCT00551512

Phase 1 Completed 48 enrolled CanBas Co. Ltd.
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this research study is to find the answers to the following questions: 1. What are the highest doses of CBP501 and cisplatin that can be safely administered as consecutive 2-hours and 1-hour infusions every 21 days? 2. What are the side effects of the combination of CBP501 and cisplatin when given as an infusion every 21 days? 3. What amount of CBP501 and cisplatin are found in the blood at certain times after it is given? 4. Are there any substances in your blood or tumor that can tell us about tumor sensitivity to CBP501 and cisplatin? 5. Will CBP501 given with cisplatin help to treat your cancer?

Timeline

Start
2006-11
Primary completion
2009-05
Completion
2009-05

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject CBP501 Peptide 3.6 mg/m2 Intravenous
Subject CBP501 Peptide 25 mg/m2 Intravenous
Subject CBP501 Peptide 36.4 mg/m2 Intravenous
Subject Cisplatin Other / unclassified 50 mg/m2 Intravenous
Subject Cisplatin Other / unclassified 75 mg/m2 Intravenous

Indications