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UnknownNCT05354089

A Study of SARS-CoV-2 mRNA Vaccine (SYS6006) in Chinese Healthy Adults Aged 18 -59 Years.

A Phase I, Randomized, Observer-blinded, Placebo-controlled and Dose-escalation Clinical Trial to Evaluate the Safety and Preliminary Immunogenicity of a SARS-CoV-2 mRNA Vaccine (SYS6006) in Chinese Healthy Adults Aged 18 -59 Years.

Status
Unknown
Phase
Phase 1
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
CSPC ZhongQi Pharmaceutical Technology Co., Ltd. · Industry
Sex
All
Age
18 Years – 59 Years
Healthy volunteers
Accepted

Summary

This is a phase I, randomized, observer-blinded, placebo-controlled and dose-escalation clinical trial to evaluate the safety, tolerability, immunogenicity and immune persistence of SYS6006 (SARS-CoV-2 mRNA Vaccine) in 18-59 year old healthy population.

Conditions

Interventions

TypeNameDescription
BIOLOGICAL20 μg dose of SYS600620 μg dose of SYS6006 vaccine IM on day 0 and day 21.
BIOLOGICAL30 μg dose of SYS600630 μg dose of SYS6006 vaccine IM on day 0 and day 21.
DRUGPlaceboPlacebo IM on day 0 and day 21.

Timeline

Start date
2022-04-27
Primary completion
2022-07-09
Completion
2023-10-01
First posted
2022-04-29
Last updated
2023-05-24

Locations

2 sites across 1 country: China

Source: ClinicalTrials.gov record NCT05354089. Inclusion in this directory is not an endorsement.