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GSK : DO NOT COURIER US FDA approves expanded age indication for GSK's Arexvy, the first respiratory syncytial virus (RSV) vaccine for adults aged 50-59 at increased risk

Over 13 million US adults aged 50-59 years have a medical condition that increases their risk of severe RSV outcomes1

Clinical development programme continues to. ....

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US FDA Approves Expanded Age Indication for GSK's AREXVY, the First Respiratory Syncytial Virus (RSV) Vaccine for Adults Aged 50-59 at Increased Risk

Over 13 million US adults aged 50-59 years have a medical condition that increases their risk of severe RSV outcomes1

Clinical development program continues to evaluate safety and immunogenicity. ....

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Ginkgo Bioworks and SaponiQx Awarded MCDC Contract to Discover and Manufacture Next-Generation Vaccine Adjuvants Using Generative Molecular Design

BOSTON and LEXINGTON, Mass., Feb. 15, 2024 /PRNewswire/ The Defense Threat Reduction Agency s Joint Science and Technology Office for the Chemical and Biological Defense Program has awarded,. ....

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GSK's RSV Vaccine, AREXVY, Accepted Under Priority Review in US for the Prevention of RSV Disease in Adults Aged 50-59 at Increased Risk -February 06, 2024 at 07:04 am EST

Application supported by positive results of a phase III trial showing immune response and acceptable tolerability profile in this population

Adults aged 50 and above with underlying medical. ....

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GSK's (GSK) RSV Vaccine, AREXVY, Accepted Under Priority Review in US

GSK's (GSK) RSV Vaccine, AREXVY, Accepted Under Priority Review in US
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