Study Phase 3

A Placebo-Controlled Study on the Effect of r-huEPO in Patients With Multiple Myeloma Followed by an Open-Label Extension

Trial Information

Generic NameEpoetin alfaProduct NamePROCRIT®Therapeutic AreaBlood and Lymph ConditionsEnrollment156% Female55%% WhiteN/A
Product ClassColony-Stimulating FactorsSponsor Protocol NumberCR005911 (EPO-INT-2)Data PartnerJohnson & JohnsonCondition StudiedAnemia, Multiple MyelomaMean/Median Age (Years)66

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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