Study Phase 3

A 6-month, Open Label, Prospective, Multicenter, International, Exploratory Study of a Transition to Flexibly Dosed Paliperidone Palmitate in Patients With Schizophrenia Previously Unsuccessfully Treated With Oral or Long-acting Injectable Antipsychotics

Trial Information

Generic NamePaliperidone palmitateProduct NameINVEGA SUSTENNA®Therapeutic AreaBehaviors and Mental DisordersEnrollment1044% Female36.9%% WhiteN/A
Product ClassAtypical AntipsychoticsSponsor Protocol NumberR092670SCH3010Data PartnerJohnson & JohnsonCondition StudiedSchizophreniaMean/Median Age (Years)38.4

Supporting Documentation

  • Collected Datasets Available
  • Protocol with Amendments Available
  • Clinical Study Report Available

Approved Data Requests Associated with this Trial

Disclaimer

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