Study Phase 3

A Randomized, Multicenter, Double-Blind, Non-inferiority Study of Paliperidone Palmitate 3 Month and 1 Month Formulations for the Treatment of Subjects With Schizophrenia

Trial Information

Generic NamePaliperidone palmitateProduct NameINVEGA SUSTENNA®Therapeutic AreaBehaviors and Mental DisordersEnrollment1429% Female46.9%% WhiteN/A
Product ClassAtypical AntipsychoticsSponsor Protocol NumberR092670PSY3011Data PartnerJohnson & JohnsonCondition StudiedSchizophreniaMean/Median Age (Years)38.6

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

Disclaimer

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