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Active, not recruiting Phase 2 Interventional Accepts healthy volunteers

Safety and Immunogenicity of CRV-101 Vaccine for the Prevention of Herpes Zoster in Adults Aged 50 Years and Older

ClinicalTrials.gov ID: NCT05304351

Public ClinicalTrials.gov record NCT05304351. 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, 4:13 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 Randomized, Observer-Blind, Phase 2 Study To Assess the Safety and Immunogenicity of CRV-101 Vaccine Head-To-Head With SHINGRIX® for the Prevention of Herpes Zoster in Adults Aged 50 Years and Older

Brief summary

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

The purpose of this study is to assess the safety and immunogenicity of amezosvatein (CRV-101), an investigational vaccine compared to Shingrix® for the prevention of herpes zoster in adults aged 50 years and older

Study identification

NCT ID
NCT05304351
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Curevo Inc
Industry
Enrollment
1,516 participants

Conditions and interventions

Eligibility (public fields only)

Age range
50 Years and older
Sex
All
Healthy volunteers
Accepts healthy volunteers

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

Study timeline

Start date
Feb 2, 2022 (Actual)
Primary completion
Jun 30, 2026 (Estimated)
Completion
Mar 6, 2032 (Estimated)
Last update posted
Sep 30, 2025

2022 – 2032

United States locations

U.S. sites
14
U.S. states
10
U.S. cities
14
Facility City State ZIP Site status
Curevo Investigational Site Tempe Arizona 85281 —
Curevo Investigational Site Coral Gables Florida 33134 —
Curevo Investigational Site Tampa Florida 33616 —
Curevo Investigational Site Oak Brook Illinois 60523 —
Curevo Investigational Site Lenexa Kansas 66219 —
Curevo Investigational Site Newton Kansas 67114 —
Curevo Investigational Site Lexington Kentucky 40509 —
Curevo Investigational Site Las Vegas Nevada 89119 —
Curevo Investigational Site Edmond Oklahoma 73013 —
Curevo Investigational Site Knoxville Tennessee 37909 —
Curevo Investigational Site Austin Texas 78745 —
Curevo Investigational Site Dallas Texas 75251 —
Curevo Investigational Site Euless Texas 76040 —
Curevo Investigational Site Salt Lake City Utah 84107 —

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 NCT05304351, 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 Sep 30, 2025 · 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 NCT05304351 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →