Study of SPG302 in Adults With Schizophrenia

Status Not yet recruiting

Clinical Trial Summary

This Phase 2 study described herein will evaluate the safety, efficacy, tolerability, and pharmacodynamics of SPG302 in adults with a primary diagnosis of schizophrenia.

Clinical Trial Description

This Phase 2 study will evaluate the safety, efficacy, tolerability, and pharmacodynamics of SPG302 in adults with a primary diagnosis of schizophrenia. This is a randomized, placebo-controlled study of SPG302 administered once daily for six weeks. This study will entail five visits to the study site for screening, study procedures, and receipt of investigational medication for use at home. ;

Study Design

Related Conditions & MeSH terms

Schizophrenia

Clinical Trial Details

NCT number	NCT06442462
Study type	Interventional
Source	Spinogenix
Contact	Leo Chen, Dr.
Phone	+61 3 9076 6564
Email	Leo.Chen@monash.edu
Status	Not yet recruiting
Phase	Phase 2
Start date	July 2024
Completion date	October 2025

View Details

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