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Celltrion Confirms Neutralising Potency Against Emerging SARS-CoV-2 Variants With Anti-COVID-19 Monoclonal Antibody Treatment regdanvimab (CT-P59)

Celltrion Confirms Neutralising Potency Against Emerging SARS-CoV-2 Variants With Anti-COVID-19 Monoclonal Antibody Treatment regdanvimab (CT-P59)
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Celltrion Confirms Neutralising Potency Against Emerging SARS-CoV-2 Variants With Anti-COVID-19 Monoclonal Antibody Treatment regdanvimab (CT-P59)

Celltrion Confirms Neutralising Potency Against Emerging SARS-CoV-2 Variants With Anti-COVID-19 Monoclonal Antibody Treatment regdanvimab (CT-P59) CT-P59 demonstrated neutralising capability against key emerging mutations, including SARS-CoV-2 variants first identified in New York (B.1.526), Nigeria (B.1.525) and India (B.1.617) 1 2  is ongoing; data expected in the coming months Celltrion is committed to assess the therapeutic neutralising antibodies against a wide array of emerging variants to end the pandemic May 17 2021, INCHEON, SOUTH KOREA - Celltrion Group today announced that CT-P59, an anti-COVID-19 monoclonal antibody treatment candidate, has confirmed neutralising potency against emerging variants first identified in New York (B.1.526), Nigeria (B.1.525) and India (B.1.617).

Celltrion Group: Regdanvimab (CT-P59), Celltrions monoklonaler Antikörper gegen COVID-19, zeigt neutralisierende Wirkung gegen die südafrikanische Virusvariante (B 1 351)

Celltrion Group: Regdanvimab (CT-P59), Celltrions monoklonaler Antikörper gegen COVID-19, zeigt neutralisierende Wirkung gegen die südafrikanische Virusvariante (B 1 351)
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EU authorises Celltrion s adalimumab biosimilar Yuflyma

EU authorises Celltrion’s adalimumab biosimilar Yuflyma 16th February 2021 The European Commission has approved Celltrion Healthcare’s Yuflyma, a biosimilar to adalimumab – marketed by AbbVie as Humira. The EC has granted the marketing authorisation for Yuflyma across all 13 indications for the treatment of a range of chronic inflammatory diseases, including rheumatoid arthritis, ulcerative colitis and psoriasis. The marketing authorisation is based on analytical, preclinical and clinical studies which demonstrated that Yuflyma is comparable to the reference product adalimumab, including in terms of efficacy and safety. Yuflyma is the first adalimumab biosimilar approved in the EU with a high concentration, low-volume and citrate-free formulation, Celltrion said in a statement.

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