Study Phase 3

Efficacy in the rHuEPO (Epoetin Alfa) in the Critically Ill Patient: A Randomized, Double Blind, Placebo-Controlled trial

Trial Information

Generic NameEpoetin alfaProduct NamePROCRIT®Therapeutic AreaBlood and Lymph ConditionsEnrollment1302% Female38%% WhiteN/A
Product ClassColony-Stimulating FactorsSponsor Protocol NumberEPO-2 /// PR98-15-014Data PartnerJohnson & JohnsonCondition StudiedAnemia, Critical IllnessMean/Median Age (Years)51

Supporting Documentation

  • Collected Datasets Available
  • Data Definition Specification Available
  • Protocol with Amendments Available
  • Statistical Analysis Plan Available
  • Clinical Study Report Available

Approved Data Requests Associated with this Trial


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