Study Phase 2

The Effect of Subcutaneous r-HuEPO in Patients With Chronic Anemia Secondary to Cisplatin Chemotherapy

Trial Information

Generic NameEpoetin alfaProduct NamePROCRIT®Therapeutic AreaBlood and Blood-Forming OrgansProduct ClassAntianemic PreparationsPharmacological SubgroupOther Antianemic PreparationsChemical SubgroupOther Antianemic PreparationsCondition StudiedAnemia
Sponsor Protocol NumberI88-036Enrollment72Data PartnerJohnson & Johnson% FemaleN/AMean/Median Age (Years)N/A% WhiteN/A

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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