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AHA Seeks Antitrust Probe of Drugmakers’ 340B Rebate Plans

The hospital lobby argues post-sale rebates replace upfront discounts, threatening safety-net providers’ finances.

Overview

  • The American Hospital Association asked the FTC and DOJ to investigate Johnson & Johnson, Eli Lilly, Bristol Myers Squibb, Sanofi and Novartis for potential collusion in rolling out 340B rebate models.
  • The request points to rapid, overlapping announcements starting with Johnson & Johnson in August 2024 and followed by the others through January, which the AHA says indicates parallel conduct.
  • Under the proposed models, providers would pay full price at purchase and seek rebates later, a shift the AHA says restricts access to discounts and effectively forces interest-free loans to manufacturers.
  • Drugmakers contend rebates help verify eligibility and reduce fraud, while a federal judge in May paused unilateral rebate rollouts but did not foreclose such models entirely.
  • HRSA launched a limited rebate pilot in August, drawing objections from hospital groups that urged extended deadlines and warned of administrative and cash-flow strain in a program that tallied $66.3 billion in 2023 purchases.