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  1. 2024年5月8日 · Bi104 granted orphan-drug designation by the U.S. Food and Drug Administration (FDA) for the treatment of Angelman syndrome (AS). Sarasota, Florida, May 08, 2024 (GLOBE NEWSWIRE) — BIOM Pharmaceutical Corporation is thrilled to announce that Bi104, its innovative drug product, has been granted orphan-drug designation by the U.S ...

  2. 2024年5月28日 · Acasti’s novel drug delivery technologies have the potential to improve the performance of currently marketed drugs by achieving faster onset of action, enhanced efficacy, reduced side effects, and more convenient drug delivery.

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  5. 6 天前 · BEERSE, BELGIUM, May 31, 2024 (GLOBE NEWSWIRE) — Janssen-Cilag International NV, a Johnson & Johnson company, announced today the submission of an application for the extension of the RYBREVANT ® (amivantamab) marketing authorisation (line extension) to the European Medicines Agency (EMA).

  6. 2024年5月28日 · The company expects to submit its New Drug Application in the third quarter. “The data from GRACE make a compelling case for the use of relacorilant in patients with endogenous hypercortisolism.

  7. 2024年5月23日 · Johnson & Johnson submits application to the European Medicines Agency seeking approval of subcutaneous formulation of RYBREVANT® (amivantamab) for the treatment of patients with EGFR-mutated non-small cell lung cancer

  8. 2024年5月3日 · Johnson & Johnson submits application to the European Medicines Agency seeking approval of subcutaneous formulation of RYBREVANT® (amivantamab) for the treatment of patients with EGFR-mutated non-small cell lung cancer