Study Phase 3

A Randomized, Double-Blind, Placebo-Controlled Study to Determine the Efficacy and Safety of Epoetin Alfa in Critically Ill Subjects

Trial Information

Generic NameEpoetin alfaProduct NamePROCRIT®Therapeutic AreaBlood and Lymph ConditionsEnrollment1460% Female37%% WhiteN/A
Product ClassColony-Stimulating FactorsSponsor Protocol NumberCR004114 (EPO-ICU-002)Data PartnerJohnson & JohnsonCondition StudiedAnemia, Critical IllnessMean/Median Age (Years)50

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

Disclaimer

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