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Regulators in the US have finalised a rule that will reduce payments for drugs provided under the 340B programme and introduce site-neutral payments in 2027, according to BioPharma Dive. Hospitals have strongly criticised the decision, which could affect their revenue streams.

This matters for healthcare executives, as the rule changes payment structures and may influence hospital budgets and drug contracting. Leaders in regulated sectors should monitor implementation and prepare for altered reimbursement models.

US finalises Medicare cuts to 340B drug payments, plans site-neutral pricing

A US federal judge has ruled that Novo did not prove Lilly’s obesity drug ad campaign, which included claims of superiority, caused meaningful harm to Novo’s sales, according to BioPharma Dive. The decision means Novo’s request to block the ads was denied.

This case matters for pharma brand leaders as it shows the limits of legal action over competitor advertising. Courts may demand clear evidence of commercial harm before restricting rival marketing. Companies should assess how they substantiate claims of injury in future disputes.

US court rejects Novo's attempt to halt Lilly obesity drug ads

Ferring will acquire Gameto, an IVF technology startup, in a deal worth up to $1.4 billion, according to BioPharma Dive. The buyout gives Ferring access to a technology that could make the in vitro fertilisation process less complex and demanding for patients.

This deal is notable for its size and focus on innovation in a tightly regulated industry. Senior executives in pharma and biotech should watch how this acquisition may shift the competitive field in IVF and influence future technology investments.

Ferring buys IVF tech firm Gameto in deal worth up to $1.4B

BioPharma Dive reports that a patient who received Bristol Myers' zola-cel, an autoimmune CAR-T therapy, died 44 days after treatment. In a separate move, Gilead has acquired a company for nearly $1.3 billion to challenge Johnson & Johnson's new psoriasis drug.

These developments raise concerns for pharma executives about the safety profile of advanced therapies and the competitive pressures in immunology. The death linked to zola-cel may prompt closer regulatory scrutiny, while Gilead's acquisition signals ongoing competition in the autoimmune market.

Bristol Myers faces safety issue after patient death from autoimmune CAR-T therapy

A new analysis from the non-profit ICER found that net launch prices for new medicines spiked significantly between 2022 and 2025, with most prices well above its cost-effectiveness guidelines, according to BioPharma Dive.

This trend puts additional scrutiny on pharma pricing and could prompt stronger responses from payers or regulators. Senior leaders in pharma and healthcare should monitor how these findings may affect reimbursement, access, and pricing negotiations.

ICER says most new drug launch prices exceed cost-effectiveness limits