drugset / Trial / NCT06032000

Evaluation of Safety and Immunogenicity of a SARS-CoV-2(Severe Acute Respiratory Syndrome Coronavirus 2) Booster Vaccine (LEM-mR203)

NCT06032000 ↗

Phase 1 Completed 20 enrolled Lemonex Inc.
RandomizedParallel-groupQuadruple-blindPrevention

Summary

A dose-escalation, double-blinded, randomized, placebo-controlled phase 1 study to assess the safety, reactogenicity, and immunogenicity of a SARS-CoV-2 Booster Vaccine (LEM-mR203) in healthy adults aged at 19 to 55 years

Timeline

Start
2023-11-06
Primary completion
2025-03-28
Completion
2025-03-28

Drugs

EvaluationDrugModalityDoseRoute
Comparator LEM-mR203 Messenger RNA (mRNA) — Intramuscular

Indications