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Recruiting Phase 2

Study to Assess the Safety, Tolerability, and Treatment Response of GXV813 in Hospitalized Adults With Schizophrenia

NCT07467993 · tracked via the Priya Life Science USA tracker
Phase
Phase 2
Started
2026-03-16
Last updated
2026-07-29

Condition(s) studied

Schizophrenia

Investigational drug(s) / intervention(s)

GXV813Placebo

GXV813: GXV813 administered orally.

Placebo: Placebo administered orally.

Study summary

The purpose of this study is to assess the efficacy, safety, and tolerability of GXV813 in the treatment of an acute episode of schizophrenia

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: 1. Participant is aged 18 to 65 years, inclusive, at screening 2. Participant is capable of providing informed consent 3. Participant has a primary diagnosis of schizophrenia, established by a comprehensive psychiatric evaluation based on the DSM-5 (American Psychiatric Association 2013) criteria and confirmed by Structured Clinical Interview for DSM-5 Clinical Trials version (SCID-5-CT) 4. Participant is willing and able to be confined to an inpatient setting for the study duration (except for the follow-up period), follow instructions, and comply with the protocol requirements 5. Participant is experiencing an acute exacerbation or relapse of psychotic symptoms, with onset less than 2 months before screening 1. The participant requires hospitalization for this acute exacerbation or relapse of symptoms 2. If already an inpatient at screening, has been hospitalized for less than 2 weeks for the current exacerbation at the time of screening 6. Positive and Negative Syndrome Scale total score between 80 and 120, inclusive, at screening a. Score of ≥ 4 (moderate or greater) for ≥ 2 of the following Positive Scale (P) items: i. Item 1 (P1; delusions) ii. Item 2 (P2; conceptual disorganization) iii. Item 3 (P3; hallucinatory behavior) iv. Item 6 (P6; suspiciousness/persecution) Exclusion Criteria: 1. Any primary DSM-5 disorder other than schizophrenia within 12 months before screening (confirmed using Structured Clinical Interview for DSM-5, Clinical Trials Version (SCID-5-CT) at screening) 2. History of treatment resistance to antipsychotic medications defined as inadequate response to two adequate courses of pharmacotherapy or previous clozapine treatment for treatment-resistant schizophrenia 3. Participants who need to be treated with drugs that are known to be moderate and strong CYP3A4 inhibitors and inducers will be excluded 4. Participants taking a long-acting injectable antipsychotic could not have received a dose of medication in the last 12 weeks (24 weeks for INVEGA TRINZA®) before baseline Other protocol-defined inclusion/exclusion criteria may apply

Primary outcome measure(s)

  • Change from baseline in Positive and Negative Symptom Scale (PANSS) total score — Baseline, Week 6
    PANSS is a 30-item rating scale used to assess the positive, negative, and general psychopathy symptoms of schizophrenia. PANSS total score ranges from 30 to 120 , where a higher score indicates greater severity.

Trial sites (16)

FacilityCityRegionStatus
Pillar Clinical Research LLC Bentonville Arkansas Recruiting
CNRI Los Angeles LLC Pico Rivera California Recruiting
Segal Institute for Clinical Research Miami Florida Recruiting
CenExel iResearch Decatur Georgia Recruiting
Uptown Research Institute LLC Chicago Illinois Recruiting
Pillar Clinical Research LLC Chicago Illinois Recruiting
Arch Clinical Trials LLC St Louis Missouri Recruiting
Novartis Investigative Site Sofia BGR Recruiting
Novartis Investigative Site Haskovo Bulgaria Recruiting
Novartis Investigative Site Kazanlak Bulgaria Recruiting
Novartis Investigative Site Lovech Bulgaria Recruiting
Novartis Investigative Site Plovdiv Bulgaria Recruiting
Novartis Investigative Site Sliven Bulgaria Recruiting
Novartis Investigative Site Sofia Bulgaria Recruiting
Novartis Investigative Site Veliko Tarnovo Bulgaria Recruiting
Novartis Investigative Site Vratsa Bulgaria Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07467993 on ClinicalTrials.gov ↗ ← All trials in the USA