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Completed Phase 2 Interventional Results available

Live Zoster Vaccine in HIV-Infected Adults on Antiretroviral Therapy

ClinicalTrials.gov ID: NCT00851786

Public ClinicalTrials.gov record NCT00851786. 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 25, 2026, 11:37 PM EDT

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

Official title

A Phase II, Randomized, Double-Blind, Placebo-Controlled Clinical Trial to Evaluate the Safety, Tolerability, and Immunogenicity of ZOSTAVAX® (Zoster Vaccine Live) in Human Immunodeficiency Virus (HIV)-1-Infected Adults on Potent Combination ART With Conserved Immune Function

Brief summary

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

Herpes zoster, or shingles, is the result of a viral infection that causes a painful skin rash, usually in older people or people with suppressed immune systems like those infected with HIV. The ZOSTAVAX vaccine has been shown to reduce the number of infections and symptoms of herpes zoster infection in people over the age of 60. The purpose of this study is to evaluate the safety, tolerability, and immunogenicity of two doses of ZOSTAVAX in HIV-1-infected adults with conserved immune function (Cd4+ T cell counts \>=200 cells/uL) virologically suppressed on potent combination antiretroviral therapy (ART).

Study identification

NCT ID
NCT00851786
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
395 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
18 Years and older
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
Apr 29, 2009 (Actual)
Primary completion
Sep 22, 2011 (Actual)
Completion
Jan 3, 2012 (Actual)
Last update posted
Nov 4, 2021

2009 – 2012

United States locations

U.S. sites
43
U.S. states
20
U.S. cities
33
Facility City State ZIP Site status
Alabama Therapeutics CRS Birmingham Alabama 35294-2050 —
University of Southern California CRS Los Angeles California 90033 —
UCLA CARE Center CRS Los Angeles California 90035 —
Stanford CRS Palo Alto California 94304-5350 —
Ucsd, Avrc Crs San Diego California 92103 —
Ucsf Aids Crs San Francisco California 94110 —
Harbor-UCLA Med. Ctr. CRS Torrance California 90502 —
University of Colorado Hospital CRS Aurora Colorado 80045 —
Denver Public Health CRS Denver Colorado 80204 —
Georgetown University CRS (GU CRS) Washington D.C. District of Columbia 20007 —
Univ. of Miami AIDS CRS Miami Florida 33136 —
The Ponce de Leon Center CRS Atlanta Georgia 30308-2012 —
Northwestern University CRS Chicago Illinois 60611 —
Rush Univ. Med. Ctr. ACTG CRS Chicago Illinois 60612 —
IHV Baltimore Treatment CRS Baltimore Maryland 21201 —
Johns Hopkins Adult AIDS CRS Baltimore Maryland 21287 —
Massachusetts General Hospital ACTG CRS Boston Massachusetts 02114 —
Brigham and Women's Hosp. ACTG CRS Boston Massachusetts 02115 —
Bmc Actg Crs Boston Massachusetts 02118 —
Beth Israel Deaconess Med. Ctr., ACTG CRS Boston Massachusetts 02215 —
Henry Ford Hosp. CRS Detroit Michigan 48202 —
Washington U CRS St Louis Missouri 63110 —
Cooper Univ. Hosp. CRS Camden New Jersey 08103 —
New Jersey Medical School- Adult Clinical Research Ctr. CRS Newark New Jersey 07103 —
Cornell CRS New York New York 10010 —
NY Univ. HIV/AIDS CRS New York New York 10016 —
HIV Prevention & Treatment CRS New York New York 10032 —
Univ. of Rochester ACTG CRS Rochester New York 14642 —
Bronx-Lebanon Hosp. Ctr. CRS The Bronx New York 10457 —
Chapel Hill CRS Chapel Hill North Carolina 27599 —
Duke Univ. Med. Ctr. Adult CRS Durham North Carolina 27710 —
Greensboro CRS Greensboro North Carolina 27401 —
Univ. of Cincinnati CRS Cincinnati Ohio 45267-0405 —
Case CRS Cleveland Ohio 44106 —
MetroHealth CRS Cleveland Ohio 44109 —
The Ohio State University Medical Center Columbus Ohio 43210 —
The Research & Education Group-Portland CRS Portland Oregon 97210 —
Hosp. of the Univ. of Pennsylvania CRS Philadelphia Pennsylvania 19104 —
Thomas Jefferson Univ. Med. Ctr. CRS Philadelphia Pennsylvania 19107 —
Pitt CRS Pittsburgh Pennsylvania 15213-2582 —
The Miriam Hosp. ACTG CRS Providence Rhode Island 02906 —
Vanderbilt Therapeutics CRS Nashville Tennessee 37204 —
University of Washington AIDS CRS Seattle Washington 98104 —

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 NCT00851786, 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 Nov 4, 2021 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00851786 live on ClinicalTrials.gov.

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