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Completed Phase 2 Interventional Results available

A Double-Blind Trial of Adjunctive Valacyclovir to Improve Cognition in Early Phase Schizophrenia

ClinicalTrials.gov ID: NCT02008773

Public ClinicalTrials.gov record NCT02008773. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 6:16 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary aim of the study is to determine the efficacy of adjunctive valacyclovir, in comparison to placebo, to improve visual (Brief Visuospatial Memory Test) and working (composite score of the Spatial Span and Letter Number Span tests) memory in individuals who are HSV-1 positive and early in the course of schizophrenia. We hypothesize that individuals who are HSV-1 positive, but not those who are HSV-1 negative, will demonstrate significant valacyclovir efficacy for visual and working memory.

Study identification

NCT ID
NCT02008773
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Indiana University
Other
Enrollment
170 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 40 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 26, 2014 (Actual)
Primary completion
Jun 20, 2017 (Actual)
Completion
Jun 20, 2017 (Actual)
Last update posted
Jan 30, 2019

2014 – 2017

United States locations

U.S. sites
13
U.S. states
7
U.S. cities
12
Facility City State ZIP Site status
C.I. Trials, Inc.-Los Angeles County Bellflower California 90706 —
University of California, Los Angeles Los Angeles California 90095 —
University of California, Riverside at C.I. Trials, Inc.-Inland Empire Riverside California 92506 —
C.I. Trials, Inc.-Orange County Santa Ana California 92705 —
Yale University New Haven Connecticut 06519 —
Innovative Clinical Research, Inc. Lauderhill Florida 33319 —
Prevention and Recovery Center for Early Psychosis Indianapolis Indiana 46202 —
Indiana University Psychotic Disorders Clinic Indianapolis Indiana 46222 —
University of Kansas Medical Center-Witchita Wichita Kansas 67214 —
Maryland Psychiatric Research Center Baltimore Maryland 21228 —
Centers for Behavioral Health, LLC Rockville Maryland 20850 —
Sheppard Pratt Health System Towson Maryland 21204 —
Laureate Institute for Brain Research Tulsa Oklahoma 74136 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02008773, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 30, 2019 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02008773 live on ClinicalTrials.gov.

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