One for the ADVFN brigade6 Jul 2024 15:55
How is Sareums SDC not comparable with Deucravacitinib?
Was it over priced in the deal?
Why did it fail in Ulcerative Colitus?
How much was paid for it?
How good was the phase 2b Pasi score?
Why are other companies creating inhibitors that they believe can out perform?
Why would SDC1802 not prove significantly better efficacy as dual inhibition over allosteric Tyk2 and the factual scientific rationale supporting this?
Why do the fools on ADVN choose to copy and paste garbage from here over on ADVN?
They know who they are.
If you think you are that clever, wolf of wolf Street sonny boy, then copy and paste this over on ADVN.
Regards
You are out of your league to answer the questions but you can at least copy and paste sonny.
Below from 2022 the deal to which our SDC1801 is in the same arena?
Under the terms of the agreement, Takeda will pay Nimbus Therapeutics $4 billion upfront, and sales-based milestone payments up to $2 billion. The transaction is expected to be finalized in the first half of 2023. Closing of the transaction is contingent on completion of review under antitrust laws, including the Hart-Scott-Rodino (HSR) Antitrust Improvements Act of 1976. Nimbus Therapeutics will retain ownership of its other research and development subsidiaries. Takeda will be solely responsible for future development and commercialization of NDI-034858 and other TYK2 inhibitors.
Regards