Junshi Biosciences Announces Positive Opinion from the European Medicines Agency’s CHMP For Toripalimab
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5h ago
SHANGHAI, July 26, 2024 (GLOBE NEWSWIRE) -- Shanghai Junshi Biosciences Co., Ltd (Junshi Biosciences, HKEX: 1877; SSE: 688180), a leading innovation-driven biopharmaceutical company dedicated to the discovery, development, and commercialization of novel therapies, and its wholly-owned subsidiary TopAlliance Biosciences Inc. (TopAlliance Biosciences), announce that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has given a positive opinion for the marketing authorization application (MAA) for toripalimab (European trade name: LOQTORZI®). The CHM ..read more
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Krystal Biotech to Report Second Quarter 2024 Financial Results on August 5, 2024
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7h ago
PITTSBURGH, July 26, 2024 (GLOBE NEWSWIRE) -- Krystal Biotech, Inc. (the “Company”) (NASDAQ: KRYS), a commercial-stage biotechnology company, today announced that it will report its second quarter 2024 financial results on Monday, August 5, 2024, prior to the open of U.S. markets. The post Krystal Biotech to Report Second Quarter 2024 Financial Results on August 5, 2024 appeared first on Bio Tech Winners ..read more
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GENFIT: Positive Opinion from EMA Committee for Ipsen’s Iqirvo® (elafibranor) in Primary Biliary Cholangitis
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7h ago
Lille (France), Cambridge (Massachusetts, United States), Zurich (Switzerland), July 26, 2024 - GENFIT (Nasdaq and Euronext: GNFT), a late-stage biopharmaceutical company dedicated to improving the lives of patients with rare and life-threatening liver diseases, today announced the positive opinion issued by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency's (EMA) for Ipsen’s Iqirvo® (elafibranor) for the treatment of Primary Biliary Cholangitis (PBC) in combination with ursodeoxycholic acid (UDCA) in adults with an inadequate response to UDCA or as a ..read more
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GENFIT : Avis positif du Comité des médicaments à usage humain (CHMP) pour l’Iqirvo® (élafibranor) d’Ipsen dans la Cholangite Biliaire Primitive
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7h ago
Lille (France), Cambridge (Massachusetts, États-Unis), Zurich (Suisse), 26 juillet 2024 - GENFIT (Nasdaq et Euronext : GNFT), une société biopharmaceutique de stade clinique avancé engagée dans l’amélioration de la vie des patients atteints de maladies rares du foie pouvant engager le pronostic vital, a annoncé aujourd'hui l'avis positif émis par le Comité des médicaments à usage humain (CHMP) de l'Agence Européenne des Médicaments (EMA) pour Iqirvo® (élafibranor) d'Ipsen dans le traitement de la cholangite biliaire primitive (CBP) en association avec l'acide ursodésoxycholique (UDCA) chez les ..read more
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Update on Regulatory Review of Lecanemab for Early Alzheimer’s Disease in the European Union
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7h ago
TOKYO and CAMBRIDGE, Mass., July 26, 2024 (GLOBE NEWSWIRE) -- Eisai Co., Ltd. (Headquarters: Tokyo, CEO: Haruo Naito, “Eisai”) and Biogen Inc. (Nasdaq: BIIB, Corporate headquarters: Cambridge, Massachusetts, CEO: Christopher A. Viehbacher, “Biogen”) announced today that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has adopted a negative opinion on the Marketing Authorization Approval (MAA) for the humanized anti-soluble aggregated amyloid-beta (Aβ) monoclonal antibody lecanemab as treatment for early AD (mild cognitive impairment due to Alzhe ..read more
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Legend Biotech Announces Preliminary Results for the Six-Months Ended June 30, 2024
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7h ago
SOMERSET, N.J., July 26, 2024 (GLOBE NEWSWIRE) -- Legend Biotech Corporation (NASDAQ: LEGN) (Legend Biotech), a global leader in cell therapy, today announced preliminary, unaudited financial results for the six-months ended June 30, 2024. The post Legend Biotech Announces Preliminary Results for the Six-Months Ended June 30, 2024 appeared first on Bio Tech Winners ..read more
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Psyence Biomed Announces Export of Nature-Derived Psilocybin to Australia and Provides Update on Upcoming Phase IIb Trial
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2d ago
Trial projected to be initiated shortly following receipt of drug product by trial sites The post Psyence Biomed Announces Export of Nature-Derived Psilocybin to Australia and Provides Update on Upcoming Phase IIb Trial appeared first on Bio Tech Winners ..read more
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TransCode Therapeutics, Inc. Announces Closing of Public Offering
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2d ago
Boston, MA — July 24, 2024 — TransCode Therapeutics, Inc. (Nasdaq: RNAZ) (“TransCode” or the “Company”), a clinical-stage RNA oncology company committed to The post TransCode Therapeutics, Inc. Announces Closing of Public Offering appeared first on Bio Tech Winners ..read more
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Intellia Therapeutics Reports Inducement Grants under Nasdaq Listing Rule 5635(c)(4)
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2d ago
CAMBRIDGE, Mass., July 24, 2024 (GLOBE NEWSWIRE) -- Intellia Therapeutics, Inc. (NASDAQ:NTLA), a leading clinical-stage gene editing company focused on revolutionizing medicine with CRISPR-based therapies, today announced that it awarded inducement grants on July 22, 2024 to its Executive Vice President and Chief Financial Officer, Edward Dulac, under Intellia’s 2024 Inducement Plan as a material inducement to employment. The post Intellia Therapeutics Reports Inducement Grants under Nasdaq Listing Rule 5635(c)(4) appeared first on Bio Tech Winners ..read more
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Oxurion Announces Results on the Extraordinary General Meeting (EGM) of 24 July 2024
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2d ago
Oxurion Announces Results on the Extraordinary General Meeting (EGM) of 24 July 2024 The post Oxurion Announces Results on the Extraordinary General Meeting (EGM) of 24 July 2024 appeared first on Bio Tech Winners ..read more
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