Clinical trial

PROCRIT (Epoetin Alfa) 60,000 Units Administered Once Every Two Weeks in Anemic…

NCT00388336 · Johnson & Johnson Pharmaceutical Research & Development, L.L.C., Industry · Completed

Key facts

NCT number NCT00388336
Title PROCRIT (Epoetin Alfa) 60,000 Units Administered Once Every Two Weeks in Anemic Cancer Patients Who Are Not Receiving Chemotherapy or Radiation Therapy
Official title A Pilot Study to Evaluate the Response Rate of PROCRIT (Epoetin Alfa) at 60,000 Units Every Two Weeks in Anemic Cancer Patients Not Receiving Chemotherapy Or Radiation Therapy
Lead sponsor Johnson & Johnson Pharmaceutical Research & Development, L.L.C., Industry
Collaborators Ortho Biotech Clinical Affairs, L.L.C. Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Anemia, Neoplasms
Intervention type Drug
Interventions Epoetin Alfa
Enrollment 57
Start date Feb 1, 2004
Completion Mar 1, 2005
First posted Oct 16, 2006
Last update posted May 18, 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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