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Terminated Phase 2 Interventional Results available

A Study to Evaluate the Anti-inflammatory Effects of Letermovir (Prevymis) in Adults With Human Immunodeficiency Virus (HIV)-1 and Asymptomatic Cytomegalovirus (CMV) Who Are on Suppressive Antiretroviral Therapy, Plus Its Effect on Chronic Inflammation, HIV Persistence and Other Clinical Outcomes.

ClinicalTrials.gov ID: NCT04840199

Public ClinicalTrials.gov record NCT04840199. 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 May 4, 2026, 5:19 AM EDT

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

Official title

Randomized, Controlled Trial to Evaluate the Anti-inflammatory Efficacy of Letermovir (Prevymis) in Adults With Human Immunodeficiency Virus (HIV)-1 and Asymptomatic Cytomegalovirus (CMV) Who Are on Suppressive ART and Its Effect on Chronic Inflammation, HIV Persistence, and Other Clinical Outcomes

Study identification

NCT ID
NCT04840199
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
NIH
Enrollment
44 participants

Conditions and interventions

Interventions

  • Letermovir Oral Tablet Drug

Drug

Eligibility (public fields only)

Age range
40 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 18, 2022
Primary completion
Nov 29, 2023
Completion
Nov 29, 2023
Last update posted
Mar 3, 2025

2022 – 2023

United States locations

U.S. sites
15
U.S. states
10
U.S. cities
14
Facility City State ZIP Site status
UCSD Antiviral Research Center CRS (Site 701) San Diego California 92103
UCSF HIV/AIDS CRS (Site 801) San Francisco California 94110
University of Colorado Hospital CRS Aurora Colorado 80045
Northwestern University CRS Chicago Illinois 60611
Massachusetts General Hospital CRS (MGH CRS) Boston Massachusetts 02114
Washington University Therapeutics (WT) CRS St Louis Missouri 63110
Weill Cornell Chelsea CRS (7804) New York New York 10010
Weill Cornell Uptown CRS (7803) New York New York 10065
University of Rochester Adult HIV Therapeutic Strategies Network CRS Rochester New York 14642
Cincinnati Clinical Research Site Cincinnati Ohio 45267
Case Clinical Research Site Cleveland Ohio 44106
Penn Therapeutics, CRS Philadelphia Pennsylvania 19104
University of Pittsburgh CRS Pittsburgh Pennsylvania 15213
Vanderbilt Therapeutics (VT) CRS Nashville Tennessee 37204
University of Washington Positive Research CRS Seattle Washington 98104-9929

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 NCT04840199, 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 Mar 3, 2025 · Synced May 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04840199 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →