Study Phase 2

A Phase II, Double-blind, Placebo-Controlled, Randomized, Dose-ranging Study of Multiple Subcutaneous Injections of Human Monoclonal Antibody to IL-12p40 (CNTO1275) in Subjects With Relapsing-remitting Multiple Sclerosis

Trial Information

Generic NameUstekinumabProduct NameSTELARA®Therapeutic AreaAntineoplastic and Immunomodulating AgentsEnrollment249% Female70.3%% WhiteN/A
Product ClassImmunosuppressantsSponsor Protocol NumberC0743T06Data PartnerJohnson & JohnsonCondition StudiedMultiple SclerosisMean/Median Age (Years)39

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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