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Five things for pharma marketers to know for Monday, September 22, 2025

CDC vaccine panel makes decision on hep b and COVID-19; FDA approves Keytruda; Neurolink’s next trial.

Heerea Rikhraj

September 22, 2025

4:00 am

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Health and Human Services Secretary Robert F. Kennedy Jr.’s appointed vaccine advisory panel decided not to vote on hepatitis b vaccines. The panel agreed to table discussions and not to adjust the current schedule for newborns just yet. (Politico)

The ACIP panel also decided to abandon broad COVID-19 recommendations. The panel said that the vaccine should be made available for all ages depending on shared clinical decision making with physicians. (Reuters)

The Food and Drug Administration approved Merck’s Keytruda injection shot. Generic and lower priced competition models of the cancer drug will be available as soon as 2028. (The New York Times)

Elon Musk’s Neuralink has planned a speech trial. The trial, starting in October, plans to test thoughts into speech. (Bloomberg)

Telehealth GLP-1 companies came under fire from the FDA after it sent warning letters to these health text platforms for their ads. Over 50 warning letters have currently been sent to pharma and healthcare companies. (STAT News)

To read last Friday’s edition of Five things for pharma marketers to know, click here.

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