|
|
|
|
|
|
|
M T Wed Th F |
|
28 January, 2026 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
The next 15 drugs subject to IRA negotiations are out, and several of the drugmakers were not involved in previous rounds. We’ll keep an eye out for any new challenges to the program. |
|
|
|
Alexis Kramer |
Editor, Endpoints News
|
|
|
|
|
|
|
by Nicole DeFeudis
|
Drugmakers will likely be able to handle the impacts of the third round of Medicare negotiations, analysts say, even as the biopharma industry continues to criticize the Biden-era program. On Tuesday, CMS unveiled the next 15 drugs up for negotiation, which include AbbVie’s Botox, Eli Lilly’s diabetes drug Trulicity, and Gilead’s HIV treatment Biktarvy. Analysts said some of the drugs were widely anticipated to make the list. They cited past negotiations, upcoming patent losses and new drug development as some reasons why the potential impacts may be modest. “With prior rounds of pricing negotiations reasonable, and several of these medicines set to lose
exclusivity in the near-term, we continue to expect that the impacts will be manageable,” BMO Capital Markets analyst Evan Seigerman said in a note to investors. | |
|
|
|
|
|
|
by Max Bayer
|
The Trump administration is asking a federal court to halt a case over the abortion pill mifepristone while the FDA undertakes a review of the drug’s safety protocols. An ongoing mifepristone review could result in superseding guidance that renders the case moot, government lawyers wrote in a memo on Tuesday. Louisiana is suing to overturn changes made to the pill's Risk Evaluation and Mitigation Strategy (REMS) in 2023, which removed an in-person dispensing requirement. Citing an updated FDA webpage on mifepristone, lawyers said the agency is working to collect more data ahead of a
"well-controlled study with adequate statistical power." Despite saying that work like this often takes "approximately a year or more to conduct," the FDA says it's hoping to complete it quicker. | |
|
|
|
|
|
|
by Ayisha Sharma
|
Teva says its latest earnings show it has officially transformed from a pure-play generics manufacturer into a biopharma company. “The hard clinical fact is we are not 'trying' to do it, but we’ve done it,” CEO Richard Francis told Endpoints News in an interview after the company’s earnings call. Although Teva expects
to lose about $1.1 billion in revenue this year for its generic version of Bristol Myers Squibb’s Revlimid, Francis emphasized that its gross margin, free cash flow and EBITDA are all growing. “How can any company lose that much revenue yet still grow those parts of the P&L? The primary way we’ve been able to do it is by having innovative products on the market — Austedo, Ajovy and Uzedy — that continue to drive growth at very strong rates,” Francis said. | |
|
|
|
|
|
|
by Anna Brown
|
More than a year after Lonza announced it will sell its capsules and health business, the Swiss CDMO said it has yet to finalize the deal with a buyer. A spokesperson said it has multiple potential bidders, but declined to add further details on who they were, how many there are, and when it hopes to close a transaction. Lonza first announced the divestiture of its CHI business back in December 2024. “Lonza continues to advance the CHI carve‑out and exit process as planned,” the spokesperson added. To potentially help it secure a buyer, Lonza said on Wednesday its CHI business saw a return to growth in 2025. Sales
rose 3.9% for the year after they declined multiple times throughout 2024. | |
|
|
|
|
|