FDA approves Sanofi and Regeneron’s Dupixent for bullous pemphigoid
Dupixent's approval was based on findings from the ADEPT Phase II/III trial.
25 June 2025
25 June 2025
Dupixent's approval was based on findings from the ADEPT Phase II/III trial.
Royalty's commitment involves tiered royalties for 15 years on global net sales of daraxonrasib.
The FDA label update boosts GE HealthCare’s Vizamyl to a market advantage despite the emergence of blood-based tests.
The total deal value of innovator drug acquisitions rose 780% between 2022 and 2024.
The drug's launch into the Chinese market follows Phase I and Phase III studies.
The collaboration will use Novoheart's mini-Heart Platform, which includes 3D bioengineered cardiac tissues.
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