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NCT05939596

A Phase I Clinical Trial to Evaluate the Safety, Tolerability, and Immunogenicity of SARS-CoV-2 Bivalent mRNA Vaccine (LVRNA021)

Status unknown Phase 1 Last updated 22 November 2023
What this trial tests

Phase 1 trial testing SARS-CoV-2 Bivalent mRNA Vaccine in SARS-CoV-2 in 60 participants. Status unknown.

Timeline
10 August 2023
Primary endpoint
28 September 2023
25 August 2024

Quick facts

Lead sponsorAIM Vaccine Co., Ltd.
PhasePhase 1
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposeprevention
Enrollment60
Start date10 August 2023
Primary completion28 September 2023
Estimated completion25 August 2024
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

AIM Vaccine Co., Ltd. — full company profile →

Who can join

18 and older, any sex, with SARS-CoV-2. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This trial is a phase I clinical trial of a SARS-CoV-2 Bivalent mRNA Vaccine (LVRNA021). The trial used a randomized, blinded, placebo-controlled design to evaluate the safety, tolerability, and preliminary immunogenicity of the trial vaccine in participants Aged 18 Years and Older who had received SARS-CoV-2 Vaccine.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of SARS-CoV-2 Bivalent mRNA Vaccine

Trials testing the same drug.

Other recruiting trials for SARS-CoV-2

Currently open trials in the same condition.

Other AIM Vaccine Co., Ltd. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05939596.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing