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Phase 3 Study of HS-10380 for Acute Schizophrenia in Chinese Adults
Sponsor: Jiangsu Hansoh Pharmaceutical Co., Ltd.
Summary
This is a Phase 3, randomized, double-blind, parallel-group, active- and placebo-controlled, multicenter inpatient study to examine the efficacy and safety of HS-10380 in adult Participants who are acutely psychotic with a Diagnostic and Statistical Manual Fifth Edition (DSM-5) diagnosis of schizophrenia. The primary objective of the study is to assess the efficacy of HS-10380 versus placebo in reducing Positive and Negative Syndrome Scale (PANSS) total scores in adult inpatients with a DSM-5 diagnosis of schizophrenia. The secondary objectives of the study are to evaluate the response rate, improvement in disease severity and symptoms, safety and tolerability.
Official title: A Randomized, Double-Blind, Active- and Placebo-Controlled Phase 3 Clinical Study Evaluating the Efficacy and Safety of HS-10380 in Chinese Adult Patients With Acute Schizophrenia
Key Details
Gender
All
Age Range
18 Years - 65 Years
Study Type
INTERVENTIONAL
Enrollment
476
Start Date
2026-11-04
Completion Date
2029-02-07
Last Updated
2026-11-03
Healthy Volunteers
No
Conditions
Interventions
HS-10380
Oral;QD;W1:dose titration; W 2-3 dose adjust to optimal level;Week 4-6:stable dose
Aripiprazole
Oral;QD;W1:dose titration; W 2-3 dose adjust to optimal level;Week 4-6:stable dose
Placebo
Oral;QD;W1:dose titration; W 2-3 dose adjust to optimal level;Week 4-6:stable dose
Locations (1)
Shanghai Mental Health Center
Shanghai, Shanghai Municipality, China