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In China, For Global

An innovative and globally competitive

biopharmaceutical company with a whole-industry-chain layout.

In China, For Global

An innovative and globally competitive

biopharmaceutical company with a whole-industry-chain layout.

Original Innovation, Science Oriented

Globally-integrated R&D process

Technology system encompassing the entire lifecycle of antibodies

Innovation-driven Biopharma

China’s leading innovative biopharmaceutical company

Established in December, 2012

Therapeutic Area

  • Oncology

    Toripalimab (PD-1), Tifcemalimab (BTLA)…

  • Autoimmune

    Adalimumab (TNF-α), JS005 (IL-17A), UBP1213sc (BLyS)

  • Metabolic

    Ongericimab (PCSK9), JS103 (Uricase), JS401 (ANGPTL3)…

  • Neurological

    JS010 (CGRP)

  • Infectious

    Etesevimab (S protein), Deuremidevir Hydrobromide (RdRp)…

Therapeutic Area

  • Oncology
  • Autoimmune
  • Metabolic
  • Neurological
  • Infectious
Learn more

Our Milestones

News Center

  • Oct 20, 2023

    Junshi Biosciences Presents 11 Clinical Trials of Toripalimab at the ESMO Congress 2023

    >SHANGHAI, China, 27, 2023 (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, announced the presentation of new clinical trial results at the European Society of Oncologists (“ESMO”) Immuno-Oncology Congress 2023, an international conference held in Madrid, Spain, from October 20th to 24th.

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  • Jun 28, 2023

    Junshi Biosciences Announces Initiation of Phase 3 Study of Tifcemalimab plus Toripalimab for Treatment of Limited-stage Small Cell Lung Cancer

    >SHANGHAI, China, June 28, 2023 (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, announced that the U.S. Food and Drug Administration (“FDA”) has recently agreed a randomized, double-blind, placebo-controlled, multi-regional phase 3 clinical study of tifcemalimab (product code: TAB004/JS004), an anti-BTLA monoclonal antibody used in combination with toripalimab, an anti-PD-1 monoclonal antibody, as consolidation therapy for patients with limited-stage small cell lung cancer without disease progression following chemoradiotherapy may proceed. Junshi Biosciences will officially initiate the phase 3 clinical study in the near future.

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  • Apr 25, 2023

    Junshi Biosciences Announces Acceptance of the New Drug Application for JS002 (anti-PCSK9 mAb)

    >SHANGHAI, China, April 25, 2023 (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, today announced the acceptance of the new drug application for the company’s recombinant humanized anti-PCSK9 monoclonal antibody (product code: JS002) by the National Medical Products Administration (“NMPA”).

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  • Apr 21, 2023

    Junshi Biosciences Announces Toripalimab plus Chemotherapy Significantly Improved Event-free Survival (EFS) versus Chemotherapy as Perioperative Treatment for Resectable Stage III Non-small Cell Lung Cancer (NSCLC) in Phase 3 Neotorch Study

    >SHANGHAI, China, April 21, 2023 (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, today announced that positive interim event-free survival (EFS) results from the Neotorch study were presented at the ASCO April Plenary Series.

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