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 Lymph ConditionsEnrollment102% Female3%% White90%
Product ClassColony-Stimulating FactorsSponsor Protocol NumberCR006076 (I88-009)Data PartnerJohnson & JohnsonCondition StudiedAIDS, AnemiaMean/Median Age (Years)39

Supporting Documentation

  • Collected Datasets Available

Approved Data Requests Associated with this Trial

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