FDA vaccines chief Vinay Prasad to leave regulator in April

The controversial head of the Food and Drug Administration's vaccines and biologics unit, Dr. ​Vinay Prasad, will leave the agency at the end of April, the agency announced on Friday.

The controversial head of the Food and Drug Administration's vaccines and biologics unit, Dr. ​Vinay Prasad, will leave the agency at the end of April, the agency announced on Friday. (Andrew Kelly, Reuters)


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KEY TAKEAWAYS
  • Dr. Vinay Prasad will leave the Food and Drug Administration's vaccines unit in April, the administration announced on Friday.
  • His tenure included disputes over COVID-19 vaccines and rare disease drugs.
  • UniQure shares rose 57% after Prasad's departure announcement.

WHITE OAK, Md. — The controversial head of the Food and Drug Administration's vaccines and biologics unit, Dr. ​Vinay Prasad, will leave the agency at the end of April.

FDA Commissioner Dr. Marty Makary posted about the departure on social media platform X, saying Prasad would return to the University of California, ‌San Francisco School of Medicine, where he is a professor, and that he had accomplished much during his one-year sabbatical.

The news was first reported ⁠by The Wall Street Journal.

Makary said a successor ​will be named before Prasad's departure.

Prasad, an oncologist, was ⁠an outspoken critic of drug and vaccine policies, particularly around COVID-19 mandates, before joining the agency. His ‌tenure included a series of ‌high‑profile disputes over product reviews for vaccines, including Moderna's COVID shot, gene therapies and other ⁠rare disease drugs.

He was appointed as the director of the FDA's ⁠Center for Biologics Evaluation and Research in May last year. Shortly after, he stepped down over questions of his handling of a muscular dystrophy treatment before returning to the role just weeks later.

UniQure shares jump 57%

Most recently, Prasad's division at the FDA engaged in a back-and-forth tussle with Dutch drugmaker UniQure over disagreements about the path forward for the company's gene therapy for Huntington's disease.

The drug regulator called ‌for a new study to support the approval of the company's gene ​therapy for the rare brain disorder, but the company and patient advocates argued that what the FDA was asking for was too lengthy and onerous on patients.

The Department of Health and Human Services, which oversees the FDA, has accused the company of misleading the public about what regulators were asking for.

U.S.-listed shares of UniQure jumped 57% in extended trading, following the news of Prasad's departure.

An opinion piece in The Wall Street Journal on Feb. 24 said the FDA had torpedoed several rare disease drugs under Prasad, ​contradicting Makary's stated goal of flexible reviews for such treatments and raising questions about the management of the health regulator.

The piece cited ‌the latest rejection ‌of Disc Medicine's ⁠treatment, which had received the commissioner's National Priority Voucher, a program launched by Makary to help fast-track breakthrough treatments.

Disc had said that the agency concluded that the trials did not show a clear link between biological improvement and clinical benefit.

Shares of Disc rose about 10% in after-market trading.

Prasad's departure is the latest reshuffle at the health department, ‌which recently put National Institutes of ​Health head Jay Bhattacharya in charge of the Centers for ‌Disease Control and Prevention following ⁠the departure of Jim ​O'Neill.

Contributing: Christy Santhosh

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The Key Takeaways for this article were generated with the assistance of large language models and reviewed by our editorial team. The article, itself, is solely human-written.

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