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Study identifier: NCT07493551 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Bioequivalence Study of PP3M in Patients With Schizophrenia

Condition: Schizophrenia  ·  Sponsor: CSPC Zhongnuo Pharmaceutical (Shijiazhuang) Co., Ltd.

PhaseNA
Planned participants260
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

To evaluate the bioequivalence of the test formulation paliperidone palmitate injection (3M) produced by CSPC Zhongnuo Pharmaceutical (Shijiazhuang) Co., Ltd. and the reference formulation paliperidone palmitate injection (3M) (brand name: Invega Trinza) by Janssen Pharmaceutica N.V. under multiple-dose administration.

This description comes directly from the study's public registry record.

Talk to the study team

Clinical Trials Information Group officer  ·  86-0311-69085587  ·  ctr-contact@cspc.cn

Always discuss trial participation with your own doctor first.

Locations (1)

Beijing Anding Hospital Capital Medical UniversityBeijing, Beijing Municipality, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07493551