drugset / Trial / NCT01631279

A Dose Escalation Trial of PR610 Treating Patients With Solid Tumors

NCT01631279 ↗

Phase 1/2 Terminated 33 enrolled Proacta, Incorporated
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the Maximum Tolerated Dose and the Dose-Limiting Toxicity of the drug to further evaluate safety and antitumor activity.

Timeline

Start
2012-08
Primary completion
2015-03
Completion
2015-08

Outcome

Outcome not reported

Stopped: “Study was prematurely discontinued due to unacceptable toxicity.”

Drugs

EvaluationDrugModalityDoseRoute
Subject PR610 Unknown — Intravenous