Merck’s $4 Billion Daiichi ADC Pact Takes Its Third FDA Setback in Three Years
The $4bn deal’s first return keeps slipping toward 2028, the year Keytruda begins to lose protection.
The $4bn deal’s first return keeps slipping toward 2028, the year Keytruda begins to lose protection.
The molecule that failed on long intervals in 2022 now holds vision with most patients on six-month dosing.
The cost gap rests on drug prices that have already moved, in a study whose funder sells surgical systems.
In Brazil the constraint on Prestige’s Herceptin biosimilar was not the dossier. It was the factory inspection.
Merck is buying into KRAS G12D at the start line, well behind the company it reportedly tried to buy in January.
Bahrain is small. The move matters as evidence of the global rollout Lilly argued a small-molecule GLP-1 would allow.
Three drugs now divide an ultra-rare disease by mechanism, route and age, and the newest competes on convenience and safety.
Constitutional challenges to Medicare negotiation have failed repeatedly. AbbVie is now betting on the definition of its product.
A drug the EMA refused two years ago is now approved, on a narrow label and under exceptional circumstances, with Europe first.
The one clean upfront among this week’s discovery deals, and Earendil keeps more of the early clinical risk than most.