Clinical trial

An Efficacy and Safety Study of PROCRIT (Epoetin Alfa) in Cancer Patients…

NCT00337948 · Johnson & Johnson Pharmaceutical Research & Development, L.L.C., Industry · Completed

Key facts

NCT number NCT00337948
Title An Efficacy and Safety Study of PROCRIT (Epoetin Alfa) in Cancer Patients Receiving Chemotherapy Every Week or Every Four Weeks
Official title An Open-Labeled Pilot Study to Evaluate the Effects of High Dose PROCRIT (Epoetin Alfa) in Maintaining Hemoglobin Levels in Anemic Cancer Patients Receiving Chemotherapy on a Weekly or Every Four Week Regimen
Lead sponsor Johnson & Johnson Pharmaceutical Research & Development, L.L.C., Industry
Collaborators Ortho Biotech Products, L.P. Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Chemotherapy, Anemia, Cancer
Intervention type Drug
Interventions Epoetin alfa
Enrollment 129
Start date Feb 1, 2003
Completion Feb 1, 2005
First posted Jun 20, 2006
Last update posted Jun 10, 2011

At a glance

  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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