{"id":2248,"date":"2023-05-07T09:01:38","date_gmt":"2023-05-07T09:01:38","guid":{"rendered":"https:\/\/www.junshipharma.com\/%e5%90%9b%e5%ae%9e%e7%94%9f%e7%89%a9%e5%ae%a3%e5%b8%83%e4%b8%8e%e7%91%9e%e8%bf%aa%e5%8d%9a%e5%a3%ab%e5%ae%9e%e9%aa%8c%e5%ae%a4%ef%bc%88dr-reddys%ef%bc%89%e8%be%be%e6%88%90%e5%90%88%e4%bd%9c\/"},"modified":"2023-05-09T09:07:44","modified_gmt":"2023-05-09T09:07:44","slug":"%e5%90%9b%e5%ae%9e%e7%94%9f%e7%89%a9%e5%ae%a3%e5%b8%83%e4%b8%8e%e7%91%9e%e8%bf%aa%e5%8d%9a%e5%a3%ab%e5%ae%9e%e9%aa%8c%e5%ae%a4%ef%bc%88dr-reddys%ef%bc%89%e8%be%be%e6%88%90%e5%90%88%e4%bd%9c","status":"publish","type":"post","link":"https:\/\/www.junshipharma.com\/en\/%e5%90%9b%e5%ae%9e%e7%94%9f%e7%89%a9%e5%ae%a3%e5%b8%83%e4%b8%8e%e7%91%9e%e8%bf%aa%e5%8d%9a%e5%a3%ab%e5%ae%9e%e9%aa%8c%e5%ae%a4%ef%bc%88dr-reddys%ef%bc%89%e8%be%be%e6%88%90%e5%90%88%e4%bd%9c\/","title":{"rendered":"Junshi Biosciences Announces Collaboration with Dr. Reddy\u2019s to Develop and Commercialize Toripalimab in 21 Countries"},"content":{"rendered":"\n
SHANGHAI, China, May 7, 2023 (GLOBE NEWSWIRE) — Shanghai Junshi Biosciences Co., Ltd (\u201cJunshi Biosciences\u201d, HKEX: 1877; SSE: 688180) announced a collaboration with Dr. Reddy\u2019s Laboratories Limited (\u201cDr. Reddy\u2019s\u201d) to develop and commercialize toripalimab, the anti-PD-1 monoclonal antibody in Latin America, India , South Africa, and at the election of Dr. Reddy\u2019s, also in Australia, New Zealand and other countries.<\/p>\n\n\n\n
\u201cWe are thrilled to have established a partnership with Dr. Reddy\u2019s while toripalimab\u2019s global commercial network has been steadily expanding, reaching more than 50 countries and advancing our mission of being \u2018In China, For Global.\u2019\u201d said Dr. Ning LI, Chief Executive Officer of Junshi Biosciences. \u201cDr. Reddy\u2019s is a well-respected global pharmaceutical company and extends its business over nearly 70 countries worldwide, achieving impressive commerical presence across the globe. We hope that in the near future, leveraging Dr. Reddy\u2019s partnership and strong presence, our innovative medicines can accelerate access to new geographies and deliver better and more affordable treatment options to even more patients.\u201d<\/p>\n\n\n\n
M.V. Ramana, CEO \u2013 Branded Markets (India & Emerging Markets), Dr. Reddy\u2019s said, \u201cWe are pleased to partner with Junshi Biosciences to take this important product to more patients. Oncology is a focus area for Dr. Reddy\u2019s. This partnership is a further step towards increasing our offerings to patients in oncology as we aim to build a robust and comprehensive portfolio in the segment. We are committed to facilitating access to innovative products as we pursue our goal of serving over 1.5 billion patients by 2030.\u201d<\/p>\n\n\n\n
Under the license and commercialization agreement, Junshi Biosciences will grant a licence to Dr. Reddy\u2019s to develop and exclusively commercialize toripalimab in Brazil, Mexico, Colombia, Argentina, Peru, Chile, Panama, Uruguay, India and South Africa[1]<\/a>. Dr. Reddy\u2019s may elect to expand the scope of the license to cover Australia, New Zealand and nine other countries[2]<\/a>.<\/p>\n\n\n\n Under the terms of the agreement, Junshi Biosciences also grants Dr. Reddy\u2019s the exclusive right of first negotiation for commercialization, in the event that Junshi Biosciences determines to grant any third party the rights to commercialize two other products as agreed in the agreement in one or more countries within the total 21 countries of Dr. Reddy\u2019s Territory[3]<\/a>.<\/p>\n\n\n\n Junshi Biosciences may receive up to an aggregate of US$728.3 million for upfront payment, potential expansion of Dr. Reddy\u2019s Territory and milestone payment, plus double-digit percentage of royalties on the net sales of products containing toripalimab.<\/p>\n\n\n\n <\/p>\n\n\n\n About Toripalimab<\/strong><\/p>\n\n\n\n Toripalimab is an anti-PD-1 monoclonal antibody developed for its ability to block PD-1 interactions with its ligands, PD-L1 and PD-L2, and for enhanced receptor internalization (endocytosis function). Blocking PD-1 interactions with PD-L1 and PD-L2 promotes the immune system\u2019s ability to attack and kill tumor cells.<\/p>\n\n\n\n More than forty company-sponsored toripalimab clinical studies covering more than fifteen indications have been conducted globally by Junshi Biosciences, including in China, the United States, Southeast Asia, and European countries. Ongoing or completed pivotal clinical trials evaluating the safety and efficacy of toripalimab cover a broad range of tumor types including cancers of the lung, nasopharynx, esophagus, stomach, bladder, breast, liver, kidney and skin.<\/p>\n\n\n\n In China, toripalimab was the first domestic anti-PD-1 monoclonal antibody approved for marketing (approved in China as TUOYI\u00ae). Currently, there are six approved indications for toripalimab in China:<\/p>\n\n\n\n <\/p>\n\n\n\n The first three indications have been included in the National Reimbursement Drug List (NRDL) (2022 Edition). Toripalimab is the only anti-PD-1 monoclonal antibody included in the NRDL for treatment of melanoma.<\/p>\n\n\n\n In the United States, the Biologics License Application (BLA) for toripalimab in combination with gemcitabine\/cisplatin, for the first-line treatment of patients with advanced recurrent or metastatic NPC and toripalimab monotherapy for the second-line or later treatment of recurrent or metastatic NPC after platinum-containing chemotherapy is under review by the U.S. Food and Drug Administration (FDA). The FDA has granted Breakthrough Therapy designations for toripalimab in combination with chemotherapy for the first-line treatment of recurrent or metastatic NPC as well as for toripalimab monotherapy in the second or third-line treatment of recurrent or metastatic NPC. Additionally, the FDA has granted Fast Track designation for toripalimab for the treatment of mucosal melanoma and Orphan Drug designations for the treatment of esophageal cancer, NPC, mucosal melanoma, soft tissue sarcoma, and small cell lung cancer (SCLC).<\/p>\n\n\n\n In Europe, marketing authorization applications (MAA) were accepted by the European Medicines Agency (EMA) and the United Kingdom\u2019s Medicines and Healthcare products Regulatory Agency (MHRA) for 1) toripalimab combined with cisplatin and gemcitabine for the first-line treatment of patients with locally recurrent or metastatic NPC and 2) toripalimab combined with paclitaxel and cisplatin for the first-line treatment of patients with unresectable locally advanced\/recurrent or metastatic ESCC, in December 2022 and February 2023.<\/p>\n\n\n\n <\/p>\n\n\n\n About Dr. Reddy\u2019s <\/strong><\/p>\n\n\n\n Dr. Reddy\u2019s is a global pharmaceutical company headquartered in Hyderabad, India and listed on the New York Stock Exchange (stock code: RDY), the National Stock Exchange of India (stock code: DRREDDY), and the Bombay Stock Exchange (stock code: 500124). Established in 1984, Dr. Reddy\u2019s is committed to providing access to affordable and innovative medicines. Driven by its purpose of \u2018Good Health Can\u2019t Wait\u2019, Dr. Reddy\u2019s offers a portfolio of products and services including APIs, generics, branded generics, biosimilars and OTC. Dr. Reddy\u2019s major therapeutic areas of focus are gastrointestinal, cardiovascular, diabetology, oncology, pain management and dermatology. Its major markets include \u2013 the United States, India, China, Brazil and Europe. As a company with a history of deep science that has led to several industry firsts, Dr. Reddy\u2019s continues to plan ahead and invest in businesses of the future. As an early adopter of sustainability and ESG actions, Dr. Reddy\u2019s released its first Sustainability Report in 2004. Its current ESG goals aim to set the bar high in environmental stewardship; access and affordability for patients; diversity; and governance. For more information, log on to: www.drreddys.com.<\/p>\n\n\n\n <\/p>\n\n\n","protected":false},"excerpt":{"rendered":" SHANGHAI, China, May 7, 2023 (GLOBE NEWSWIRE) — Shanghai Junshi Biosciences Co., Ltd (\u201cJunshi Biosciences\u201d, HKEX: 1877; SSE: 688180) announced a collaboration with Dr. Reddy\u2019s Laboratories Limited (\u201cDr. Reddy\u2019s\u201d) to develop and commercialize toripalimab, the anti-PD-1 monoclonal antibody in Latin America, India , South Africa, and at the election of Dr. Reddy\u2019s, also in Australia, New Zealand and other countries.<\/p>\n","protected":false},"author":3,"featured_media":1117,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[22],"tags":[],"class_list":["post-2248","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-uncategorized"],"yoast_head":"\n[1]<\/a> Collectively, \u201cDr. Reddy\u2019s Territory 1\u201d<\/h5>\n\n\n\n
[2]<\/a> Collectively, \u201cDr. Reddy\u2019s Territory 2\u201d<\/h5>\n\n\n\n
[3]<\/a> Both \u201cDr. Reddy\u2019s Territory 1\u201d and \u201cDr. Reddy\u2019s Territory 2\u201d are collectively known as \u201cDr. Reddy\u2019s Territory\u201d, totalling 21 countries.<\/h5>\n\n\n\n\n\n
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