drugset / Trial / NCT01110603

A Study of MK-4827 in Combination With Standard Chemotherapy in Participants With Advanced Solid Tumors (MK-4827-008 AM1)

NCT01110603

Phase 1 Terminated 12 enrolled Tesaro, Inc.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This study will find the dose limiting toxicities (DLTs), maximum tolerated dose (MTD), and recommended Phase 2 dose (RPTD) of MK4827 when administered in combination with standard doses of carboplatin, or carboplatin/paclitaxel, or carboplatin/liposomal doxorubicin in the treatment of advanced solid cancers in adults.

Timeline

Start
2010-07
Primary completion
2011-07
Completion
2011-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Niraparib Small molecule 40 mg Oral
Background Carboplatin Small molecule Intravenous
Background Doxorubicin Other / unclassified 30 mg/m2 Intravenous
Background Paclitaxel Small molecule 175 mg/m2 Intravenous

Indications

No indication recorded.