ClinicalTrials.gov record
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 May 20, 2026, 7:02 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

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

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

Interventions

  • Amezosvatein Adjuvant Dose Arm D Biological
  • Amezosvatein Adjuvant Dose Arm F Biological
  • Amezosvatein Adjuvant Dose Arm H Biological
  • Amezosvatein Adjuvant Dose Arm J Biological
  • Amezosvatein Adjuvant Dose Arm L Biological
  • Amezosvatein Antigen High Dose Arm A Biological
  • Amezosvatein Antigen Low Dose Arm B Biological
  • Shingrix Biological

Biological

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 1, 2022
Primary completion
Jun 29, 2026
Completion
Mar 5, 2032
Last update posted
Sep 29, 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 29, 2025 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05304351 live on ClinicalTrials.gov.

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