Study Phase 3

A clinical evaluation of the effect of maintaining haemoglobin levels with weekly EPREX®/ERYPO® (Epoetin alfa) in subjects with lymphoid malignancies (Hodgkin's Disease, Non-Hodgkin's Lymphoma, Chronic Lymphocytic Leukemia and Multiple Myeloma) undergoing chemotherapy

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  • Globe symbol for NCT Number NCT Number Not Available
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Trial Information

Generic NameEpoetin alfaProduct NamePROCRIT®Therapeutic AreaBlood and Blood-Forming OrgansProduct ClassAntianemic PreparationsPharmacological SubgroupOther Antianemic PreparationsChemical SubgroupOther Antianemic PreparationsCondition StudiedAnemia
Sponsor Protocol NumberOBE/EPO-INT-02Enrollment1000Data PartnerJohnson & Johnson% FemaleN/AMean/Median Age (Years)58.9% WhiteN/A

Supporting Documentation

  • Collected Datasets Available
Additional Information

Three narratives are available upon data request approval for Study OBE-EPO-INT-02: Subjects With Disease Progression, Subjects Who Died, and Subjects with Thrombovascular Events.

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