Clinical Trials Directory

Trials / Completed

CompletedNCT06145178

A Study of Human Cytomegalovirus (HCMV) Vaccine SPYVLP01 With and Without Adjuvants

A Phase I First in Human Study to Assess Safety and Immunogenicity of the Human Cytomegalovirus Vaccine Candidate SPYVLP01 With and Without Adjuvants in Healthy Adult Volunteers

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
120 (actual)
Sponsor
SpyBiotech Limited · Industry
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

The main purpose of the study is to evaluate the safety and immunogenicity of SPYVLP01 in two different doses with and without adjuvants in healthy adults aged 18-50 years old.

Conditions

Interventions

TypeNameDescription
BIOLOGICALSPYVAC01Novel vaccine SPYVLP01

Timeline

Start date
2023-11-22
Primary completion
2025-06-20
Completion
2025-07-09
First posted
2023-11-24
Last updated
2025-09-22

Locations

2 sites across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT06145178. Inclusion in this directory is not an endorsement.