drugset / Trial / NCT00796055

Study of MEDI-547 to Evaluate the Safety, Tolerability, and Biologic Activity of IV Administration in Subjects With Relapsed or Refractory Solid Tumors

NCT00796055 ↗

Phase 1 Terminated 6 enrolled MedImmune LLC
RandomizedSingle-groupOpen-labelTreatment

Summary

To determine the safety, tolerability, and the highest dose of this drug given once every 3 weeks or once every week, (per 21 day cycle) in adult subjects with relapsed or refractory solid tumors.

Timeline

Start
2009-08
Primary completion
2010-02
Completion
2010-06

Outcome

Outcome not reported

Stopped (Business): “MI-CP177 study closed per sponsor decision.”

Drugs

EvaluationDrugModalityDoseRoute
Subject MEDI-547 Unknown — Intravenous

Indications