drugset / Trial / NCT00825487

Dose Escalation Study of ARQ 621 in Adult Patients With Metastatic Solid Tumors and Hematologic Malignancies

NCT00825487 ↗

Phase 1 Completed 50 enrolled ArQule, Inc.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This is an open-label, dose escalation study of intravenous ARQ 621 administered to patients with late-stage solid tumors or hematologic malignancies.

Timeline

Start
2009-08
Primary completion
2011-05
Completion
2011-09

Drugs

EvaluationDrugModalityDoseRoute
Subject ARQ 621 Small molecule 10 mg/m2 Intravenous
Subject ARQ 621 Small molecule 200 mg/m2 Intravenous

Indications