Study Phase 3

A 24-month, Prospective, Randomized, Active-Controlled, Open-Label, Rater-Blinded, Multicenter, International Study of the Prevention of Relapse Comparing Long-Acting Injectable Paliperidone Palmitate to Treatment as Usual With Oral Antipsychotic Monotherapy in Adults With Schizophrenia

  • 1 CSR Summary Not Yet Available
  • 1 NCT01081769
  • 1 Primary Citation Not Available
  • Data Specification Not Available

Trial Information

Generic NamePaliperidone palmitateProduct NameINVEGA SUSTENNA®Therapeutic AreaBehaviors and Mental DisordersEnrollment769% Female41.6%% WhiteN/A
Product ClassAtypical AntipsychoticsSponsor Protocol NumberR092670SCH3005Data PartnerJohnson & JohnsonCondition StudiedSchizophreniaMean/Median Age (Years)32.5

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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