A Safety and Immunogenicity Trial of a Respiratory Syncytial Virus Vaccine, LYB005 in Healthy Adults

PHASE1Active, not recruitingINTERVENTIONAL
Enrollment

84

Participants

Timeline

Start Date

July 31, 2024

Primary Completion Date

December 30, 2025

Study Completion Date

December 30, 2025

Conditions
Respiratory Syncytial Virus (RSV)RSV Infection
Interventions
BIOLOGICAL

LYB005 low dose without adjuvant

Dosage forms and strengths: Solution for injection. Administer a single dose (0.5 mL) as an intramuscular injection.

BIOLOGICAL

LYB005 middle dose without adjuvant

Dosage forms and strengths: Solution for injection. Administer a single dose (0.5 mL) as an intramuscular injection.

BIOLOGICAL

LYB005 high dose without adjuvant

Dosage forms and strengths: Solution for injection. Administer a single dose (0.5 mL) as an intramuscular injection.

BIOLOGICAL

LYB005 low dose with adjuvant

Dosage forms and strengths: Solution for injection. Administer a single dose (0.5 mL) as an intramuscular injection.

BIOLOGICAL

LYB005 middle dose with adjuvant

Dosage forms and strengths: Solution for injection. Administer a single dose (0.5 mL) as an intramuscular injection.

BIOLOGICAL

LYB005 high dose with adjuvant

Dosage forms and strengths: Solution for injection. Administer a single dose (0.5 mL) as an intramuscular injection.

BIOLOGICAL

Placebo

0.9% sodium chloride injection. Dosage forms and strengths: Solution for injection. Administer a single dose (0.5 mL) as an intramuscular injection.

BIOLOGICAL

Positive control

AREXVY. Dosage forms and strengths: Solution for injection. Administer a single dose (0.5 mL) as an intramuscular injection.

Trial Locations (1)

Unknown

Nucleus Network Pty Ltd., Melbourne

All Listed Sponsors
collaborator

Yantai Patronus Biotech Co., Ltd.

INDUSTRY

lead

Guangzhou Patronus Biotech Co., Ltd.

INDUSTRY

NCT06442241 - A Safety and Immunogenicity Trial of a Respiratory Syncytial Virus Vaccine, LYB005 in Healthy Adults | Biotech Hunter | Biotech Hunter