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NCT07467993PHASE2Recruiting

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

Novartis Pharmaceuticals

Start Date

3/16/2026

Completion Date

7/29/2027

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 Criteria

Age Range: 18 years to 65 years

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

Interventions

DRUG

GXV813

DRUG

Placebo

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Conditions

Schizophrenia

Locations

Pillar Clinical Research LLC

Bentonville, Arkansas 72712

United States

CNRI Los Angeles LLC

Pico Rivera, California 90660

United States

Segal Institute for Clinical Research

Miami, Florida 33016

United States

CenExel iResearch

Decatur, Georgia 30030

United States

Uptown Research Institute LLC

Chicago, Illinois 60640

United States

Pillar Clinical Research LLC

Chicago, Illinois 60641

United States

Arch Clinical Trials LLC

St Louis, Missouri 63141

United States

Novartis Investigative Site

Sofia, BGR 1431

Bulgaria

Novartis Investigative Site

Haskovo, 6300

Bulgaria

Novartis Investigative Site

Kazanlak, 6100

Bulgaria

Novartis Investigative Site

Lovech, 5500

Bulgaria

Novartis Investigative Site

Plovdiv, 4002

Bulgaria

Novartis Investigative Site

Sliven, 8800

Bulgaria

Novartis Investigative Site

Sofia, 1377

Bulgaria

Novartis Investigative Site

Veliko Tarnovo, 5000

Bulgaria

Novartis Investigative Site

Vratsa, 3000

Bulgaria