Last updated on July 2019

A Study to Evaluate the Safety and Immunogenicity of an Adjuvanted RSV Vaccine in Healthy Older Adults


Brief description of study

The study will evaluate the safety, tolerability, and immunogenicity of up to 7 different RSV vaccine candidates, some with adjuvant, when administered concomitantly with seasonal inactivated influenza vaccine (SIIV).

Detailed Study Description

The study will evaluate the safety, tolerability, and immunogenicity of up to 7 different RSV vaccine candidates, some with adjuvant, when administered concomitantly with SIIV. Healthy male and female subjects between 65 to 85 years of age will be enrolled. Subjects will receive 2 intramuscular injections to assess the concomitant administration of SIIV when given to subjects receiving one of the 3 RSV vaccine dose-level candidates formulated with or without an adjuvant.

Clinical Study Identifier: NCT03572062

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Clinical Research of South Florida

Coral Gables, FL United States
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Qps Mra, Llc

South Miami, FL United States
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Optimal Research, LLC

Peoria, IL United States
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Laverty Pathology

Adamstown, Australia
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Eastern Health

Box Hill, Australia
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Pharmacy Department

Camberwell, Australia
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Monash Health

Clayton, Australia
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TrialsWest

Murdoch, Australia
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Mater Hospital

South Brisbane, Australia
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Mater Misericordiae Limited

South Brisbane, Australia
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Barwon Health

Geelong, Australia
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