drugset / Trial / NCT00700336

Study of CBP501 + Pemetrexed + Cisplatin on MPM (Phase I/II)

NCT00700336

Phase 1/2 Completed 69 enrolled CanBas Co. Ltd.
RandomizedParallel-groupOpen-labelTreatment

Summary

The phase I part of the study is a dose-finding study of escalating doses of CBP501 combined with full-dose cisplatin and pemetrexed in patients with histologically confirmed solid malignancy that is metastatic or unresectable and for which standard curative or palliative measures do not exist or are no longer effective or would otherwise be eligible for cisplatin and pemetrexed as first-line therapy. The maximum tolerated dose (MTD) will be determined based on DLTs occurring during the first treatment cycle. Pharmacokinetics of the triplet combination will be assessed during the phase I part of the trial. The phase II part will evaluate full-dose cisplatin and pemetrexed combined with CBP501 (at the MTD determined in the phase I part) in previously untreated, unresectable malignant pleural mesothelioma patients. Patients will be randomized in a 2 : 1 ratio to pemetrexed, cisplatin and CBP501 (Arm A) or to pemetrexed and cisplatin (Arm B); randomization will be stratified according to histology and performance status.

Timeline

Start
2008-05
Primary completion
2012-07
Completion
2012-11

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject CBP501 Peptide 16 mg/m2 Intravenous
Subject CBP501 Peptide 25 mg/m2 Intravenous
Background Cisplatin Other / unclassified 75 mg/m2
Background Pemetrexed Small molecule 500 mg/m2