drugset / Trial / NCT00350090

A Study to Assess the Response Rate of PROCRIT (Epoetin Alfa) Given at a Dose of 40,000 Units Once a Week to Cancer Patients With Anemia Who Are Not Receiving Chemotherapy.

NCT00350090 ↗

Phase 3 Terminated 98 enrolled Ortho Biotech Products, L.P.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the effectiveness and safety of PROCRIT (Epoetin alfa) administered at 40,000 Units weekly in cancer patients that are not receiving chemotherapy or radiation therapy.

Timeline

Start
2002-09
Primary completion
—
Completion
2004-03

Outcome

Outcome not reported

Stopped (Enrollment): “This study was stopped early due to slow enrollment.”

Drugs

EvaluationDrugModalityDoseRoute
Subject epoetin alfa Protein / enzyme biologic 40000 iu Subcutaneous

Indications