drugset / Trial / NCT01204996

A Study of the Safety and Efficacy of CNTO 888 in Combination With SoC (Standard of Care) Chemotherapy in Patients With Solid Tumors

NCT01204996 ↗

Phase 1 Completed 53 enrolled Centocor, Inc.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety and dose regimen of CNTO 888 when administered to patients with solid tumors in combination with 4 standard of care chemotherapy regimens.

Timeline

Start
2010-05
Primary completion
—
Completion
2011-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Carboplatin Small molecule 6 unknown —
Subject Carlumab Monoclonal antibody 10 mg/kg Intravenous
Subject Carlumab Monoclonal antibody 15 mg/kg Intravenous
Subject Docetaxel Small molecule 75 mg/m2 —
Subject Doxorubicin Other / unclassified 50 mg/m2 Intravenous
Subject Gemcitabine Small molecule 1000 mg/m2 —
Subject Paclitaxel Small molecule 175 mg/m2 —

Indications