Innovent and Lilly Expand Collaboration Through Agreement on Commercialization Rights for Jaypirca (Pirtobrutinib) in Mainland China
Innovent and Lilly Expand Collaboration Through Agreement on Commercialization Rights for Jaypirca (Pirtobrutinib) in Mainland China
SAN FRANCISCO and SUZHOU, China, Dec. 15, 2024 /PRNewswire/ -- Innovent Biologics, Inc. ("Innovent") (HKEX: 01801), a world-class biopharmaceutical company that develops, manufactures and commercializes high-quality medicines for the treatment of oncology, autoimmune, cardiovascular and metabolic, ophthalmology and other major diseases, and Eli Lilly and Company (NYSE: LLY) today jointly announced a Distribution and Promotion Agreement in Mainland China regarding Lilly's non-covalent (reversible) Bruton's tyrosine kinase (BTK) inhibitor, Jaypirca (pirtobrutinib, 100 mg & 50 mg tablets). The agreement highlights the following aspects:
SAN FRANCISCO and SUZHOU, China, Dec. 15, 2024 /PRNewswire/ -- Innovent Biologics, Inc. ("Innovent") (HKEX: 01801), a world-class biopharmaceutical company that develops, manufactures and commercializes high-quality medicines for the treatment of oncology, autoimmune, cardiovascular and metabolic, ophthalmology and other major diseases, and Eli Lilly and Company (NYSE: LLY) today jointly announced a Distribution and Promotion Agreement in Mainland China regarding Lilly's non-covalent (reversible) Bruton's tyrosine kinase (BTK) inhibitor, Jaypirca (pirtobrutinib, 100 mg & 50 mg tablets). The agreement highlights the following aspects:
- Innovent will be responsible for the importation, marketing, distribution and promotion of Jaypirca;
- Lilly will be responsible for the R&D and post-market medical affairs of Jaypirca.
- Innovent will be responsible for the importation, marketing, distribution and promotion of Jaypirca;
- Lilly will be responsible for the R&D and post-market medical affairs of Jaypirca.
Jaypirca, a highly selective kinase inhibitor, utilizes a novel non-covalent binding mechanism to re-establish BTK inhibition in mantle cell lymphoma (MCL) patients previously treated with a covalent BTK inhibitor (approved including ibrutinib, acalabrutinib, zanubrutinib, or orelabrutinib) and extend the benefit of targeting the BTK pathway, thus effectively addressing the unmet clinical needs for these patients. Approved by the U.S. FDA in January 2023, Jaypirca (pirtobrutinib) became the first and only approved non-covalent (reversible) BTK inhibitor. In October 2024, Jaypirca (pirtobrutinib) received approval from China's National Medical Products Administration (NMPA) as monotherapy for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (MCL) after at least two types of systemic therapy, including a Bruton's tyrosine kinase (BTK) inhibitor (Link).
Jaypirca, a highly selective kinase inhibitor, utilizes a novel non-covalent binding mechanism to re-establish BTk inhibition in mantle cell lymphoma (MCL) patients previously treated with a covalent BTk inhibitor (approved including ibrutinib, acalabrutinib, zanubrutinib, or orelabrutinib) and extend the benefit of targeting the BTk pathway, thus effectively addressing the unmet clinical needs for these patients. Approved by the U.S. FDA in January 2023, Jaypirca (pirtobrutinib) became the first and only approved non-covalent (reversible) BTk inhibitor. In October 2024, Jaypirca (pirtobrutinib) received approval from China's National Medical Products Administration (NMPA) as monotherapy for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (MCL) after at least two types of systemic therapy, including a Bruton's tyrosine kinase (BTK) inhibitor (Link).
Lilly is conducting comprehensive global Phase 3 development programs (including in China), in first-line and relapse or refractory patients with chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL), and BTK inhibitor-naïve relapse or refractory MCL, to explore monotherapy or combination therapy.
Lilly is conducting comprehensive global Phase 3 development programs (including in China), in first-line and relapse or refractory patients with chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL), and BTk inhibitor-naïve relapse or refractory MCL, to explore monotherapy or combination therapy.
Under the agreement, Innovent holds the sole commercialization rights for Jaypirca in Mainland China, overseeing importation, marketing, distribution and promotion. Lilly will be responsible for R&D and post-market medical affairs. Leveraging Innovent's established hematology oncology commercial team and Lilly's deep expertise in drug development and scientific insights in the therapeutic area, the partnership is committed to broadening access to innovative treatments and improving outcomes for cancer patients in Mainland China.
根據協議,君實生物在中國大陸擁有Jaypirca的獨家商業化權利,負責進口、市場營銷、分銷和推廣。禮來則負責研發和市場後醫療事務。通過利用君實生物的建立的血液腫瘤商業團隊以及禮來在藥物開發和治療領域深厚的專業知識,該合作伙伴關係致力於拓寬創新治療的獲得途徑,並改善中國大陸癌症患者的治療效果。
Dr. Michael Yu, Founder, Chairman and CEO of Innovent, stated: "Building on our long-term strategic collaboration with Lilly, we are proud to expand our collaboration through this agreement. Jaypirca, the world's first and only approved non-covalent (reversible) BTK inhibitor, represents a breakthrough treatment option for patients who have previously received BTK inhibitors. Innovent has built a robust and leading portfolio in the hematological malignancy field, consisting of TYVYT (sintilimab injection), HALPRYZA (rituximab injection), olverembatinib, FUCASO (Equecabtagene Autoleucel Injection), and Jaypirca. By fully leveraging our commercialization capabilities and extensive coverage in this field, we aim to bring forward innovative medicines to benefit cancer patients and further enhance our leading position in oncology. We remain steadfast in our commitment to advancing the biopharmaceutical industry through collaborative efforts so that first-rate pharmaceutical drugs can become widely accessible."
君實生物創始人、董事長兼CEO於明介紹說:"基於我們與禮來的長期戰略合作關係,我們很自豪能夠通過這項協議擴大我們的合作。Jaypirca是全球首個也是唯一獲批的非共價(可逆)BTk抑制劑,代表了對曾經接受BTk抑制劑患者的突破性治療選擇。君實生物在血液惡性腫瘤領域建立了強大而領先的產品組合,包括TYVYt(信迪利單抗注射液)、HALPRYZA(利妥昔單抗注射液)、olverembatinib、FUCASO(Equecabtagene Autoleucel注射液)及Jaypirca。通過充分利用我們的商業化能力及該領域的廣泛覆蓋,我們旨在推出創新藥物以惠及癌症患者,並進一步提升我們在腫瘤學領域的領導地位。我們堅定致力於通過協作努力推動生物製藥行業的發展,以便一流的藥品能廣泛可得。"
Huzur Devletsah, President and General Manager of Lilly China, states, "Lilly is thrilled to appoint Innovent for the distribution and promotion of Jaypirca marking a pivotal moment in hematologic cancer treatment for Lilly. This agreement allows to rapidly increase patient access in Mainland China by drawing on Innovent's robust market presence and our extensive R&D expertise. Together, we are poised to deliver innovative therapies and support the 'Healthy China 2030' initiative, continuing our commitment: 'In China, For China."
禮來中國總裁兼總經理Huzur Devletsah表示:"禮來非常高興任命君實生物負責Jaypirca的分銷和推廣,這標誌着禮來在血液癌症治療方面的重要時刻。這項協議使我們能夠通過藉助君實生物強大的市場影響力和我們豐富的研發專業知識,迅速增加中國大陸患者的獲得途徑。我們共同準備提供創新療法,並支持「健康中國2030」倡議,繼續我們的承諾:'在中國,爲中國。'
About Jaypirca (pirtobrutinib)
關於Jaypirca(pirtobrutinib)
Jaypirca (pirtobrutinib, formerly known as LOXO-305) is a highly selective (300 times more selective for BTK versus 98% of other kinases tested in preclinical studies), non-covalent (reversible) inhibitor of the enzyme BTK.[i] BTK is a validated molecular target found across numerous B-cell leukemias and lymphomas including mantle cell lymphoma.[ii],[iii]
Jaypirca(pirtobrutinib,前稱LOXO-305)是一種高度選擇性的(在前期臨床研究中針對BTk的選擇性是其他98%激酶的300倍),非共價(可逆)酶BTk抑制劑。[i] BTk是一個經過驗證的分子靶點,存在於包括外套細胞淋巴瘤在內的多種b細胞白血病和淋巴瘤中。[ii],[iii]
About Innovent's strategic cooperation with Lilly
關於Innovent與Lilly的戰略合作
Innovent and Lilly have established a comprehensive level of cooperation, setting an example of partnership between a Chinese innovative pharmaceutical company and a global leading medicine company in the field of R&D, CMC, clinical development and commercialization, aiming to accelerate the access of innovative medicines to benefit more patients worldwide.
Innovent與Lilly已建立全面合作,成爲中國創新藥品公司與全球領先製藥公司在研發、CMC、臨床開發和商業化領域合作的典範,旨在加速創新藥品的可及性,使更多患者受益於全球。
In March 2015, Innovent entered into a strategic partnership with Lilly focused on biological medicine. Under the initial agreement, Lilly and Innovent co-developed and co-commercialized oncology medicines, including Tyvyt (sintilimab injection) in China. In October 2015, the two parties announced the extension of collaboration to include the co-development of three additional antibodies in oncology. In August 2019, the cooperation extended with a licensing agreement for the development and commercialization of a potentially global best-in-class investigational GCG/GLP-1 medicine in China. In August 2020, Innovent and Lilly announced a global expansion of their strategic alliance for sintilimab. In March 2022, Lilly and Innovent deepened their engagement in oncology, granting Innovent sole commercialization rights for Cyramza (ramucirumab) and Retsevmo (selpercatinib), and a right of first negotiation for potential future commercialization of Jaypirca (pirtobrutinib) in Mainland China. In December 2024, the agreement of the commercialization of Jaypirca (pirtobrutinib) in Mainland China officially achieved.
2015年3月,Innovent與Lilly簽署了戰略合作協議,專注於生物藥品。在初步協議下,Lilly與Innovent共同開發和商業化包括在中國的Tyvyt(sintilimab注射液)在內的腫瘤藥物。2015年10月,雙方宣佈將合作擴展至共同開發三種額外的腫瘤抗體。2019年8月,合作通過一項授權協議進一步擴展,用於在中國開發和商業化一種潛在的全球最佳藥品GCG/GLP-1。2020年8月,Innovent與Lilly宣佈其戰略聯盟在sintilimab領域的全球擴展。2022年3月,Lilly與Innovent加深了在腫瘤領域的合作,授予Innovent獨家商業化Cyramza(ramucirumab)和Retsevmo(selpercatinib)的權利,並對未來在中國大陸的Jaypirca(pirtobrutinib)潛在商業化進行優先協商的權利。2024年12月,Jaypirca(pirtobrutinib)在中國大陸的商業化協議正式達成。
About Innovent Biologics
關於Innovent生物技術
Innovent is a leading biopharmaceutical company founded in 2011 with the mission to empower patients worldwide with affordable, high-quality biopharmaceuticals. The company discovers, develops, manufactures and commercializes innovative medicines that target some of the most intractable diseases. Its pioneering therapies treat cancer, cardiovascular and metabolic, autoimmune and eye diseases. Innovent has launched 12 products in the market. It has 5 new drug applications under regulatory review, 3 assets in Phase III or pivotal clinical trials and 17 more molecules in early clinical stage. Innovent partners with over 30 global healthcare companies, including Eli Lilly, Sanofi, Incyte, Adimab, LG Chem and MD Anderson Cancer Center.
Innovent是一家成立於2011年的領先生物製藥公司,使命是爲全球患者提供負擔得起的高質量生物製藥。該公司發現、開發、生產及商業化針對一些最棘手疾病的創新藥物。其開創性療法用於治療癌症、心血管和代謝、自身免疫以及眼科疾病。Innovent已經推出12種產品。它有5項新藥申請正在接受監管審查,3項資產處於III期或關鍵臨床試驗中,另外還有17種分子處於早期臨床階段。Innovent與超過30家全球醫療保健公司合作,包括禮來、賽諾菲安萬特、因塞特、Adimab、LG Chem和MD安德森癌症中心。
Guided by the motto, "Start with Integrity, Succeed through Action," Innovent maintains the highest standard of industry practices and works collaboratively to advance the biopharmaceutical industry so that first-rate pharmaceutical drugs can become widely accessible. For more information, visit , or follow Innovent on Facebook and LinkedIn.
在「以誠信爲起點,通過行動獲得成功」的座右銘指引下,創新藥業保持行業最佳實踐的最高標準,並共同努力推動生物製藥行業,以便一流的藥品能夠廣泛獲得。欲了解更多信息,請訪問,或在Facebook和LinkedIn上關注創新藥業。
Statement:
(1)Innovent does not recommend the use of any unapproved drug (s)/indication (s).
(2)Ramucirumab (Cyramza), Selpercatinib (Retsevmo) and Pirtobrutinib (Jaypirca) were developed by Eli Lilly and Company.
聲明:
(1)創新藥業不推薦使用任何未經批准的藥物/適應症。
(2)Ramucirumab (Cyramza)、Selpercatinib (Retsevmo)和Pirtobrutinib (Jaypirca)由禮來公司開發。
About Eli Lilly and Company
關於禮來公司
Lilly is a medicine company turning science into healing to make life better for people around the world. We've been pioneering life-changing discoveries for nearly 150 years, and today our medicines help tens of millions of people across the globe. Harnessing the power of biotechnology, chemistry and genetic medicine, our scientists are urgently advancing new discoveries to solve some of the world's most significant health challenges: redefining diabetes care; treating obesity and curtailing its most devastating long-term effects; advancing the fight against Alzheimer's disease; providing solutions to some of the most debilitating immune system disorders; and transforming the most difficult-to-treat cancers into manageable diseases. With each step toward a healthier world, we're motivated by one thing: making life better for millions more people. That includes delivering innovative clinical trials that reflect the diversity of our world and working to ensure our medicines are accessible and affordable. To learn more, visit .
禮來是一家制藥公司,將科學轉化爲治癒,以改善全球人們的生活。我們已經在改變生命的發現方面開拓了近150年的歷史,如今我們的藥物幫助了全球數千萬的人。利用生物技術、化學和基因醫學的力量,我們的科學家們緊急推動新發現,以解決世界上一些最重要的健康挑戰:重新定義糖尿病護理;治療肥胖並減少其最具破壞性的長期影響;推進阿爾茨海默病的鬥爭;爲一些最嚴重的免疫系統疾病提供解決方案;並將最難治療的癌症轉變爲可管理的疾病。在邁向更健康的世界的每一步中,我們的動力源於一個目標:讓數百萬人的生活變得更好。這包括提供反映我們世界多樣性的創新臨床試驗,以及確保我們的藥物可獲得且負擔得起。欲了解更多信息,請訪問。
Forward-Looking Statements of Innovent Biologics
創新藥業生物製品的前瞻性聲明
This news release may contain certain forward-looking statements that are, by their nature, subject to significant risks and uncertainties. The words "anticipate", "believe", "estimate", "expect", "intend" and similar expressions, as they relate to Innovent Biologics, Inc. ("Innovent" or "Company"), are intended to identify certain of such forward-looking statements. The Company does not intend to update these forward-looking statements regularly.
本新聞稿可能包含某些前瞻性聲明,這些聲明本質上受到重大風險和不確定性的限制。"預期"、"相信"、"估計"、"期待"、"打算"和類似表達方式,均與創新藥業股份有限公司("創新藥業"或"公司")有關,意在識別某些此類前瞻性聲明。公司不打算定期更新這些前瞻性聲明。
These forward-looking statements are based on the existing beliefs, assumptions, expectations, estimates, projections and understandings of the management of the Company with respect to future events at the time these statements are made. These statements are not a guarantee of future developments and are subject to risks, uncertainties and other factors, some of which are beyond the Company's control and are difficult to predict. Consequently, actual results may differ materially from information contained in the forward-looking statements as a result of future changes or developments in our business, the Company's competitive environment and political, economic, legal and social conditions.
這些前瞻性聲明是基於公司管理層在做出這些聲明時對未來事件的現有信念、假設、期望、估計、預測和理解。這些聲明並不是對未來發展的保證,並且受到風險、不確定性和其他一些超出公司控制範圍的因素的影響,因此很難預測。因此,由於我們業務、公司競爭環境以及政治、經濟、法律和社會條件的未來變化或發展,實際結果可能與前瞻性聲明中包含的信息有實質性差異。
The Company, the Directors and the employees of the Company assume (a) no obligation to correct or update the forward-looking statements contained in this site; and (b) no liability in the event that any of the forward-looking statements does not materialize or turn out to be incorrect.
公司、董事和公司員工假設(a) 不承擔糾正或更新本網站中包含的前瞻性聲明的任何義務;以及(b) 如果任何前瞻性聲明未能實現或被證明是不正確的,則不承擔任何責任。
References
參考文獻
[i] Mato AR, Shah NN, Jurczak W, et al. Pirtobrutinib in relapsed or refractory B-cell malignancies (BRUIN): a phase 1/2 study. Lancet. 2021;397(10277):892-901. doi:10.1016/S0140-6736(21)00224-5 |
[ii] Hanel W, Epperla N. Emerging therapies in mantle cell lymphoma. J Hematol Oncol. 2020;13(1):79. Published 2020 Jun 17. doi:10.1186/s13045-020-00914-1 |
[iii] Gu D, Tang H, Wu J, Li J, Miao Y. Targeting Bruton tyrosine kinase using non-covalent inhibitors in B cell malignancies. J Hematol Oncol. 2021;14(1):40. Published 2021 Mar 6. doi:10.1186/s13045-021-01049-7 |
[i] Mato AR, Shah NN, Jurczak W等。Pirtobrutinib在復發或難治性B細胞惡性腫瘤中的應用(BRUIN):一項1/2期研究。柳葉刀。2021;397(10277):892-901. doi:10.1016/S0140-6736(21)00224-5 |
[ii] Hanel W, Epperla N。外套細胞淋巴瘤的新興治療。血液學與腫瘤學雜誌。2020;13(1):79. 發佈於2020年6月17日。doi:10.1186/s13045-020-00914-1 |
[iii] Gu D, Tang H, Wu J, Li J, Miao Y。使用非共價抑制劑靶向Bruton酪氨酸激酶用於B細胞惡性腫瘤。血液學與腫瘤學雜誌。2021;14(1):40. 發佈於2021年3月6日。doi:10.1186/s13045-021-01049-7 |
SOURCE Innovent Biologics
來源:信達生物製品