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Around the Districts: Clonroche-Poulpeasty to Fethard

CLONROCHE-POULPEASTY

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Junshi Biosciences and Coherus Announce Positive Final Overall Survival Results of JUPITER-02, a Phase 3 Clinical Trial Evaluating Toripalimab as Treatment for Recurrent or Metastatic Nasopharyngeal Carcinoma

- Final overall survival analysis of the JUPITER-02 trial shows first-line treatment with toripalimab plus chemotherapy significantly prolongs survival in patients with advanced NPC - SHANGHAI, China

United statesDennis riedlPatricia keeganJunshi bioscienceJunshi topalliance biosciencesMarek ciszewskiRosh diasJodi sieversJunshi biosciencesCoherus biosciencesZhi liExchange commission onIr teamCoherus biosciences incExchange commissionVp corporate communications

Coherus (CHRS) and Junshi Report Positive Final Overall Survival Results of JUPITER-02

Coherus (CHRS) and Junshi Report Positive Final Overall Survival Results of JUPITER-02
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United statesSan franciscoPatricia keeganJunshi bioscienceJunshi topalliance biosciencesMarek ciszewskiRosh diasJodi sieversJunshi biosciencesCoherus biosciencesZhi liExchange commission onIr teamCoherus biosciences incShanghai junshi biosciences co ltdExchange commission

Junshi Biosciences seeks UK s marketing authorisation for toripalimab

Shanghai Junshi Biosciences has submitted a marketing authorization application (MAA) for its toripalimab to the MHRA of the UK.

United kingdomPatricia keeganJunshi biosciencesJunshi topalliance biosciencesChina national medical products administrationEuropean medicines agencyDrug administrationTopalliance biosciencesBreakthrough therapy designationsOrphan drug designation

Investegate |Junshi Biosciences Announcements | Junshi Biosciences: Junshi Biosciences Announces Submission of a Marketing Authorization Application for Toripalimab to the UK Medicines and Healthcare Products Regulatory Agency

Investegate announcements from Junshi Biosciences, Junshi Biosciences Announces Submission of a Marketing Authorization Application for Toripalimab to the UK Medicines and Healthcare Products Regulatory Agency

United statesUnited kingdomSan franciscoPatricia keeganJunshi bioscienceJunshi biosciencesZhi liJunshi topalliance biosciencesAmerican society of clinical oncologyIr teamWorld health organizationRegulatory agencyNational reimbursement drug listEu european commissionEuropean medicines agencyPr team

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