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Celltrion Healthcare: Celltrion announces positive results for its cocktail therapy candidates including neutralisation data against Omicron variant

CT-P63 demonstrated a well- established safety profile in the global Phase I trial CT-P63 maintained strong neutralising ability against the Omicron variant (B.1.1.529) based on structural

Kostenloser wertpapierhandelDonna curranNational institutes of healthEuropean medicines agencyCelltrion groupCommittee for medicinal products human useMarketing division at celltrion healthcareNational institutesHoung kimMarketing divisionMedicinal productsHuman useCelltrion healthcare

Celltrion announces positive results for its cocktail therapy candidates including neutralisation data against Omicron variant

Celltrion Group announced today results for its cocktail therapy candidates including neutralisation data against the Omicron variant (B.1.1.529). The Phase I clinical trial is a randomised, double- blind and placebo- controlled trial designed to evaluate the safety, tolerability and pharmacokinetics of CT-P63 in 24 healthy subjects in Poland.1 The study met its primary objectives with data showing CT-P63 to be safe and well tolerated, with no significant drug- related adverse events (AEs).

South koreaInch on gwangyoksiDonna curranNational institutes of healthEuropean medicines agencyCelltrion groupCommittee for medicinal products human useMarketing division at celltrion healthcareNational institutesHoung kimMarketing divisionMedicinal productsHuman useCelltrion healthcareMedia contactR houng kim

Celltrion announces positive results for its cocktail therapy candidates including neutralisation data against Omicron variant

Celltrion Group announced today results for its cocktail therapy candidates including neutralisation data against the Omicron variant (B.1.1.529). The Phase .

Donna curranNational institutes of healthEuropean medicines agencyCelltrion groupCommittee for medicinal products human useMarketing division at celltrion healthcareBusiness wireNational institutesHoung kimMarketing divisionCelltrion healthcareMedicinal productsHuman use

Celltrion s monoclonal antibody treatment for COVID-19, regdanvimab (CT-P59) becomes the first authorized COVID-19 treatment approved from the Korean Ministry of Food and Drug Safety (MFDS)

Celltrion s monoclonal antibody treatment for COVID-19, regdanvimab (CT-P59) becomes the first authorized COVID-19 treatment approved from the Korean Ministry of Food and Drug Safety (MFDS)
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United kingdomInch on gwangyoksiSouth koreaRepublic of koreaDonna curranKorean ministry of foodCelltrion groupMarketing division at celltrion healthcareKorean ministryDrug safetyBusiness wireConditional marketing authorisationHoung kimMarketing divisionCelltrion healthcareஒன்றுபட்டது கிஂக்டம்

El tratamiento con anticuerpos monoclonales de Celltrion para la COVID-19, regdanvimab (CT-P59), se convierte en el primer tratamiento autorizado para la COVID-19 aprobado por el Ministerio de Seguridad Alimentaria y de Medicamentos (MFDS) de

El tratamiento con anticuerpos monoclonales de Celltrion para la COVID-19, regdanvimab (CT-P59), se convierte en el primer tratamiento autorizado para la COVID-19 aprobado por el Ministerio de Seguridad Alimentaria y de Medicamentos (MFDS) de
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Inch on gwangyoksiSouth koreaUnited statesUnited kingdomRepublic of koreaSouth koreansDonna curranFidel deltaGroup celltrionMinistry of foodSouth korea the group celltrionMfds koreans southHoung kimsDivision of medicalUntil septemberEnd notes