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Chongqing Genrix’s GR1803 Earns Breakthrough Therapy Designation in China for RRMM Treatment
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The Center for Drug Evaluation (CDE) of China has indicated that Chongqing Genrix Bio Pharmaceutical Co., Ltd (SHA: 688443) is on track to receive Breakthrough Therapy Designation (BTD) for its bispecific antibody GR1803. This designation is for the treatment of recurrent refractory multiple myeloma (RRMM) in patients who have previously…
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Genrix Bio and Chongqing Pharmaceutical Group Form Strategic Partnership to Boost Market Launch
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Chongqing Genrix Bio Pharmaceutical Co., Ltd (SHA: 688443), a biopharmaceutical company based in China, has entered into a partnership with fellow Chinese firm Chongqing Pharmaceutical (Group) Co., Ltd (CQP). Under this collaboration, Genrix Bio will utilize CQP’s extensive network and digital services to bolster the market launch of its innovative…
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Genrix Bio Pharmaceutical Partners with China Resource Medicine for Expanded Market Coverage
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Chongqing Genrix Bio Pharmaceutical Co., Ltd (SHA: 688443), a Chinese biopharmaceutical company, has entered into a strategic partnership with China Resource Medicine Commercial Holdings Ltd. The collaboration aims to enhance channel management and strengthen presence in the healthcare and retail markets. Financial details of the agreement were not disclosed. By…
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Chongqing Genrix Bio Pharmaceutical Gets NMPA Clearance for IL-4Rα mAb Candidate GR1802
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Chongqing Genrix Bio Pharmaceutical Co., Ltd (SHA: 688443), a Chinese biopharmaceutical company, has announced that it has received clinical trial clearance from the National Medical Products Administration (NMPA) for its investigational drug candidate GR1802, an interleukin-4 receptor α (IL-4Rα) monoclonal antibody (mAb). The drug is intended to be assessed as…
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Genrix Bio Seeks China Approval for New Xeligekimab Use in Axial Spondyloarthritis
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Chongqing Genrix Bio Pharmaceutical Co., Ltd. (SHA: 688443), a biopharmaceutical company based in China, has submitted a new indication filing for its innovative biologic product xeligekimab, which has now been accepted for review by the National Medical Products Administration (NMPA). This latest filing seeks approval for xeligekimab to treat radiologically…
