--- title: "XPOVIO®在韓國獲得了第二個多發性骨髓瘤適應症的報銷批准" type: "News" locale: "zh-HK" url: "https://longbridge.com/zh-HK/news/277380539.md" description: "XPOVIO® 已獲得韓國國家健康保險服務的報銷批准，用於治療成年多發性骨髓瘤（MM）的第二個適應症。該批准自 2026 年 3 月 1 日起生效，允許在接受過一次前期治療後，將 XPOVIO® 與硼替佐米和地塞米松聯合使用。開發公司安騰生物（Antengene Corporation）旨在提升患者在亞太地區對其療法的獲取，XPOVIO® 已在多發性骨髓瘤和瀰漫性大 B 細胞淋巴瘤（DLBCL）方面獲得多個適應症的批准" datetime: "2026-03-02T00:40:56.000Z" locales: - [zh-CN](https://longbridge.com/zh-CN/news/277380539.md) - [en](https://longbridge.com/en/news/277380539.md) - [zh-HK](https://longbridge.com/zh-HK/news/277380539.md) --- # XPOVIO®在韓國獲得了第二個多發性骨髓瘤適應症的報銷批准 _\- XPOVIO® is the first XPO1 inhibitor approved for reimbursement by South Korea's National Health Insurance Service (NHIS) for the treatment of adult patients with multiple myeloma (MM)._ _\- In South Korea, XPOVIO® has been approved for three indications across MM and diffuse large B-cell lymphoma (DLBCL), and two of these approved indications have been included in the national reimbursement scheme._ SHANGHAI and HONG KONG, March 1, 2026 /PRNewswire/ -- Antengene Corporation Limited (**"Antengene"**, SEHK: 6996.HK) , a leading innovative, commercial-stage global biotech company dedicated to discovering, developing and commercializing first-in-class and/or best-in-class medicines for autoimmune disease, solid tumors and hematological malignancies indications, announced that **South Korea's National Health Insurance Service (NHIS) has approved the reimbursement of XPOVIO® (selinexor) in combination with bortezomib and dexamethasone for the treatment of adult patients with multiple myeloma (MM) after one prior therapy. The reimbursement has taken effect on March 1, 2026. This marks the second XPOVIO® indication to be approved for reimbursement in South Korea.** As Antengene continues to expand its footprint across the Asia Pacific region, the Company remains committed to improving patient access to its innovative therapies. **To date, XPOVIO® has been approved in South Korea for three indications in MM and diffuse large B-cell lymphoma (DLBCL), both major hematological malignancies. Two of these indications have been approved for reimbursement**, including XPOVIO® in combination with dexamethasone for the treatment of adult patients with relapsed or refractory MM (R/R MM) who have received at least four prior therapies, as well as the newly reimbursed indication. With expanded reimbursement coverage, XPOVIO® is expected to benefit a broader patient population and further contribute to the management of hematological malignancies in South Korea. With a novel mechanism of action, XPOVIO® is the world's first approved orally-available, selective XPO1 inhibitor. XPOVIO® has already been approved in ten countries and regions in APAC, and has been included in the national insurance schemes in five of these markets (the mainland of China, Taiwan market, Australia, Singapore and South Korea). Moving forward, Antengene will continue to pursue broader access for XPOVIO® across APAC markets. **About Antengene** Antengene Corporation Limited (**"Antengene"**, SEHK: 6996.HK) is a global, R&D-driven, commercial-stage biotech company focused on developing first-in-class/best-in-class therapeutics for diseases with significant unmet medical needs. Its pipeline spans from preclinical to commercial stages and includes several in-house discovered programs, including ATG-022 (CLDN18.2 ADC), ATG-037 (oral CD73 inhibitor), ATG-101 (PD-L1 × 4-1BB bispecific antibody), and ATG-042 (oral PRMT5-MTA inhibitor). Antengene has also developed AnTenGager™, a proprietary T cell engager 2.0 platform featuring "2+1" bivalent binding for low expressing targets, steric hindrance masking, and proprietary CD3 sequences with fast on/off kinetics to minimize cytokine release syndrome (CRS) and enhance efficacy. These characteristics support the platform's broad applicability across autoimmune disease, solid tumors and hematological malignancies, with programs targeting CD19 x CD3 (ATG-201 for B cell-related autoimmune diseases), CDH6 x CD3 (ATG-106 for ovarian cancer and kidney cancer), ALPPL2 x CD3 (ATG-112 for gynecologic tumors and non-small cell lung cancer), LY6G6D x CD3 (ATG-110 for microsatellite-stable colorectal cancer), GPRC5D x CD3 (ATG-021 for multiple myeloma), LILRB4 x CD3 (ATG-102 for acute myeloid leukemia and chronic myelomonocytic leukemia) and FLT3 x CD3 (ATG-107 for acute myeloid leukemia). To date, Antengene has obtained 32 investigational new drug (IND) approvals in the U.S. and Asia, and obtained new drug application (NDA) approvals in 10 Asia Pacific markets. Its lead commercial asset, XPOVIO® (selinexor), is approved in the Mainland of China, Taiwan China, Hong Kong China, Macau China, South Korea, Singapore, Malaysia, Thailand, Indonesia and Australia, and has been included in the national insurance schemes in five of these markets (Mainland of China, Taiwan China, Australia, South Korea and Singapore). **Forward-looking statements** The forward-looking statements made in this article relate only to the events or information as of the date on which the statements are made in this article. Except as required by law, we undertake no obligation to update or revise publicly any forward-looking statements, whether as a result of new information, future events or otherwise, after the date on which the statements are made or to reflect the occurrence of unanticipated events. You should read this article completely and with the understanding that our actual future results or performance may be materially different from what we expect. In this article, statements of, or references to, our intentions or those of any of our Directors or our Company are made as of the date of this article. Any of these intentions may alter in light of future development. For a further discussion of these and other factors that could cause future results to differ materially from any forward-looking statement, please see the other risks and uncertainties described in the Company's Annual Report for the year ended December 31, 2024, and the documents subsequently submitted to the Hong Kong Stock Exchange. For more information, please contact: Investor Contacts: Donald Lung E-mail: donald.lung@antengene.com BD Contacts: Ariel Guo E-mail: ariel.guo@antengene.com View original content to download multimedia:https://www.prnewswire.com/news-releases/xpovio-receives-reimbursement-approval-in-south-korea-for-a-second-multiple-myeloma-indication-302700200.html SOURCE Antengene Corporation Limited ### 相關股票 - [512290.CN](https://longbridge.com/zh-HK/quote/512290.CN.md) - [516820.CN](https://longbridge.com/zh-HK/quote/516820.CN.md) - [516500.CN](https://longbridge.com/zh-HK/quote/516500.CN.md) - [159859.CN](https://longbridge.com/zh-HK/quote/159859.CN.md) - [560600.CN](https://longbridge.com/zh-HK/quote/560600.CN.md) - [06996.HK](https://longbridge.com/zh-HK/quote/06996.HK.md) - [512010.CN](https://longbridge.com/zh-HK/quote/512010.CN.md) - [516930.CN](https://longbridge.com/zh-HK/quote/516930.CN.md) - [159837.CN](https://longbridge.com/zh-HK/quote/159837.CN.md) - [159849.CN](https://longbridge.com/zh-HK/quote/159849.CN.md) - [159992.CN](https://longbridge.com/zh-HK/quote/159992.CN.md) - [588130.CN](https://longbridge.com/zh-HK/quote/588130.CN.md) - [588250.CN](https://longbridge.com/zh-HK/quote/588250.CN.md) - [510660.CN](https://longbridge.com/zh-HK/quote/510660.CN.md) - [588860.CN](https://longbridge.com/zh-HK/quote/588860.CN.md) ## 相關資訊與研究 - [軒竹生物安奈拉唑鈉藥新療法獲批開展 III 期臨牀，拓幽門螺桿菌治療](https://longbridge.com/zh-HK/news/282756607.md) - [映恩生物成人乳腺癌的新藥上市申請 獲得國家藥品監督管理局受理 推動在內地、香港及澳門商業化](https://longbridge.com/zh-HK/news/282618607.md) - [生華科獲國際資本青睞 與 GEM 簽署 MOU 獲 5 億元額度支持新藥研發](https://longbridge.com/zh-HK/news/282645308.md) - [金斯瑞生物科技發佈 2025 年 ESG 報告，以系統化管治與創新實踐引領可持續增長](https://longbridge.com/zh-HK/news/282738104.md) - [軒竹生物-B：安奈拉唑鈉新適應症獲批開展 III 期臨牀試驗](https://longbridge.com/zh-HK/news/282751635.md)