RECRUITING

Randomized Withdrawal Study in Patients With Schizophrenia

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The purpose of this research is to evaluate the efficacy of dosing iloperidone long-acting injection (LAI) compared to placebo in preventing the exacerbation of symptoms in patients with schizophrenia.

Official Title

A Multicenter, Double-Blind, Randomized Withdrawal Study in Patients With Schizophrenia Receiving Either Iloperidone Long-Acting Injection (LAI) or Placebo Injection

Quick Facts

Study Start:2025-05-14
Study Completion:2027-11
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06961968

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 65 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Males or females 18 to 65 years of age (inclusive)
  2. * Diagnosed with schizophrenia per DSM-5 criteria
  3. * In need of ongoing psychiatric treatment
  1. * DSM-5 diagnosis of a psychiatric disorder other than schizophrenia that was the primary focus of treatment within the previous six months

Contacts and Locations

Study Contact

Vanda Pharmaceuticals Inc.
CONTACT
202-734-3400
clinicaltrials@vandapharma.com

Study Locations (Sites)

Vanda Investigational Site
San Diego, California, 92102
United States
Vanda Investigational Site
Richardson, Texas, 75080
United States

Collaborators and Investigators

Sponsor: Vanda Pharmaceuticals

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-05-14
Study Completion Date2027-11

Study Record Updates

Study Start Date2025-05-14
Study Completion Date2027-11

Terms related to this study

Keywords Provided by Researchers

  • Schizophrenia
  • Antipsychotic Agents
  • Iloperidone
  • Long-Acting Injection
  • Randomized Withdrawal

Additional Relevant MeSH Terms

  • Schizophrenia