A Study to Evaluate the Safety, Reactogenicity and Immunogenicity of Vaccine CVSQIV in Healthy Adults

NCT05252338 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 240

Last updated 2023-06-06

No results posted yet for this study

Summary

This study aims to evaluate the safety and reactogenicity profile of CVSQIV at different dose levels.

Conditions

Interventions

BIOLOGICAL

CVSQIV

Participants will receive an intramuscular injection by needle in the deltoid area.

Sponsors & Collaborators

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
SEQUENTIAL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-02-07
Primary Completion
2022-09-27
Completion
2022-09-27

Countries

  • Panama

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05252338 on ClinicalTrials.gov