Clinical trial

Alternate Dosing of PROCRIT (Epoetin Alfa) in Patients With Cancer and…

NCT00338299 · Johnson & Johnson Pharmaceutical Research & Development, L.L.C., Industry · Completed

Key facts

NCT number NCT00338299
Title Alternate Dosing of PROCRIT (Epoetin Alfa) in Patients With Cancer and Chemotherapy Induced Anemia
Official title An Open-Label Pilot Study to Evaluate the Effects of Alternate Dosing of PROCRIT (Epoetin Alfa) in the Treatment of Patients With Cancer and Chemotherapy Induced Anemia (60,000 Units Weekly for Four Weeks Followed by 60,000 Units Every Two Weeks)
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 Anemia, Chemotherapy
Intervention type Drug
Interventions Epoetin alfa
Enrollment 51
Start date Aug 1, 2003
Completion Apr 1, 2004
First posted Jun 20, 2006
Last update posted May 23, 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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