Study Phase 4

A Randomized, Open-Label, Multicenter Study Evaluating Thrombovascular Events in Subjects With Cancer Receiving Chemotherapy and Administered Epoetin Alfa Once or Three Times a Week for the Treatment of Anemia

  • 1 CSR Summary Not Available
  • 1 NCT01394991
  • 1 Primary Citation Not Yet Available
  • Data Specification Not Available

Trial Information

Generic NameEpoetin alfaProduct NamePROCRIT®Therapeutic AreaBlood and Lymph ConditionsEnrollment504% FemaleN/A% WhiteN/A
Product ClassHematologic AgentsSponsor Protocol NumberEPOANE4008Data PartnerJohnson & JohnsonCondition StudiedAnemia, NeoplasmsMean/Median Age (Years)N/A

Supporting Documentation

  • Collected Datasets Available
  • Data Definition Specification Available
  • Protocol with Amendments Available
  • Statistical Analysis Plan Available
  • Clinical Study Report Available

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