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pharminent June 19, 2026 (Last updated: June 19, 2026)

Moderna’s mRNA Flu Vaccine Wins Unanimous FDA Panel Backing

Strategic News Watch — June 19, 2026

An FDA advisory panel handed Moderna a unanimous 9-0 endorsement for its mRNA flu vaccine — reversing the agency’s earlier refusal to review it — as AbbVie closed in on an $11 billion takeover of Apogee Therapeutics and Washington opened a trade probe into German drug pricing.

Today’s top developments:

  • Moderna’s mRNA flu vaccine mRNA-1010 (mFlusiva) won unanimous (9-0) FDA advisory committee backing in adults 50 and older (BioPharma Dive)
  • AbbVie neared a roughly $11 billion all-cash acquisition of Apogee Therapeutics (Reuters)
  • The US opened a Section 301 probe into German “underpayment” for medicines (pharmaphorum)
  • MSD won FDA approval to expand its Capvaxive pneumococcal vaccine to children aged 2 to 17 (pharmaphorum)
  • Eli Lilly began eliminating 340B discounts to hospitals over data compliance (STAT)
  • Denali Therapeutics sold an FDA priority review voucher for $195 million (BioSpace)
  • Experts urged the FDA to pause its Commissioner’s National Priority Review Voucher program (BioSpace)

What to Watch

  • Moderna mRNA-1010 FDA Decision: With the advisory panel’s unanimous backing, attention turns to the FDA’s action date of August 5, 2026 — and whether the 65-and-older indication clears as an accelerated approval tied to the planned confirmatory trial.
  • AbbVie–Apogee Announcement: A formal deal could land as early as Monday, June 22, 2026; watch for confirmed terms, the immunology assets gained, and any rival bid given the reported ~60% premium.
  • German Drug-Pricing Probe: The Section 301 comment window runs June 25 to August 10, 2026, with a September 22, 2026 hearing — escalation could test the 15% pharma tariff cap in the US-EU trade deal.
  • 340B Program Tensions: Lilly’s discount eliminations may embolden other manufacturers to impose similar data requirements, potentially reshaping the 340B landscape and triggering legislative or regulatory responses.
  • FDA Voucher Program Reevaluation: Calls to pause the Commissioner’s National Priority Review Voucher program could prompt added transparency requirements or a rethink of how expedited-review candidates are selected.

This brief highlights the edition’s top stories. Read the latest edition → for all stories and analysis.

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