Study Phase 2

A Double-Blind, Placebo-Controlled Study With Open-Label Follow-up to Determine the Safety and Efficacy of Subcutaneous Doses of r-HuEPO in AIDS Patients With Anemia Induced by Their Disease and AZT Therapy

Trial Information

Generic NameEpoetin alfaProduct NamePROCRIT®Therapeutic AreaBlood and Blood-Forming OrgansProduct ClassAntianemic PreparationsPharmacological SubgroupOther Antianemic PreparationsChemical SubgroupOther Antianemic PreparationsCondition StudiedAIDS, Anemia
Sponsor Protocol NumberCR006076 (I88-009)Enrollment102Data PartnerJohnson & Johnson% Female3.0%Mean/Median Age (Years)39.0% White90.0%

Supporting Documentation

  • Collected Datasets Available
  • Data Definition Specification Available
  • Clinical Study Report Available

Approved Data Requests Associated with this Trial

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