Core Viewpoint - Fosun Pharma's subsidiary has received acceptance for a drug registration application for the treatment of Langerhans cell histiocytosis (LCH) in children aged 2 and above, which has been included in the priority review process by the National Medical Products Administration (NMPA) [1] Group 1: Drug Development and Approval - The drug, Rumaine (generic name: Luwomeitini tablets), is already approved in China for two indications: treatment of LCH in adults and treatment of symptomatic, inoperable plexiform neurofibromas in children and adolescents with Neurofibromatosis Type 1 (NF1) [1] - The drug is currently in Phase III clinical trials for the treatment of adult NF1 and low-grade gliomas in children, and in Phase II clinical trials for the treatment of extra-cranial arteriovenous malformations [1] - The NMPA has included the drug for the treatment of inoperable or residual/recurrent NF1-related plexiform neurofibromas in adults in its breakthrough therapy program [1] Group 2: Financial Investment and Market Potential - As of October 2025, the cumulative R&D investment for the drug is approximately RMB 638 million (unaudited) [2] - According to IQVIA MIDAS™ data, the global sales for MEK1/2 selective inhibitors are projected to be approximately USD 2.068 billion in 2024 [2]

Core Viewpoint - Fosun Pharma's subsidiary has received acceptance for a drug registration application for Rumaine (generic name: Luwomeitini tablets) to treat children aged 2 and above with Langerhans cell histiocytosis (LCH), which is now included in the priority review process by the National Medical Products Administration (NMPA) [1] Group 1: Drug Development and Approval - The drug has already been approved in China for two indications: treatment of LCH and adult patients with tissue cell tumors, and treatment of symptomatic, inoperable plexiform neurofibromas (PN) in children and adolescents with Neurofibromatosis type 1 (NF1) [1] - The drug is currently in Phase III clinical trials for treating adult NF1 and low-grade gliomas in children, and in Phase II clinical trials for treating extra-cranial arteriovenous malformations [1] - The drug for treating inoperable or residual/recurrent NF1-related plexiform neurofibromas in adult patients has been included in the breakthrough therapy program by the NMPA [1] Group 2: Financial Investment and Market Potential - As of October 2025, the cumulative R&D investment for this drug is approximately RMB 638 million (unaudited) [2] - According to IQVIA MIDAS™ data, the global sales of MEK1/2 selective inhibitors are projected to be approximately USD 2.068 billion in 2024 [2]

Core Viewpoint - Fosun Pharma's subsidiary has received acceptance for a drug registration application for Rumaine (generic name: Lenvatinib) to treat children aged 2 and above with Langerhans Cell Histiocytosis (LCH), which has been included in the priority review process by the National Medical Products Administration [1] Group 1: Drug Information - Rumaine is a selective MEK1/2 inhibitor [1] - The drug has already been approved for two indications in China: treatment of LCH in adult patients and treatment of symptomatic, inoperable plexiform neurofibromas (PN) in children and adolescents aged 2 and above with Neurofibromatosis Type 1 (NF1) [1]

Core Viewpoint - The article emphasizes the journey and vision of Fosun Pharma under the leadership of Chairman Chen Yuqing, focusing on innovation, global expansion, and the integration of AI in drug development and operations [3][10][20]. Group 1: Company Background and Leadership - Chen Yuqing transitioned from academia to the corporate world 26 years ago, eventually becoming the Chairman of Fosun Pharma in April 2025 [1][3]. - Under his leadership, Fosun Pharma has grown into a nearly 100 billion yuan global innovative pharmaceutical company, with a strong emphasis on corporate culture that fosters innovation and talent development [3][4]. Group 2: Innovation and Product Development - Fosun Pharma has consistently prioritized innovation, launching 12 innovative drugs since 2019, including the first CAR-T product in China and the first PD-1 monoclonal antibody approved for small cell lung cancer [4][6]. - The company’s innovative drug revenue exceeded 4.3 billion yuan in the first half of 2025, accounting for 31% of its pharmaceutical business revenue, with a year-on-year growth of 14.26% [8][10]. Group 3: Globalization Strategy - Fosun Pharma's globalization strategy focuses on building local capabilities rather than merely exporting products, with over 1,000 personnel in its overseas commercialization team and a marketing network covering over 110 countries [10][12]. - The company has established regional distribution centers in emerging markets and has supplied over 420 million doses of anti-malarial products globally, significantly impacting public health [13][20]. Group 4: AI Integration in Operations - Fosun Pharma is actively integrating AI into its operations, utilizing the PharmAID decision-making platform to enhance drug development efficiency, reducing target validation time by over 60% [14][15]. - The company emphasizes that while AI is a powerful tool for enhancing efficiency, it cannot replace the intrinsic value of human expertise and understanding of patient needs [16][17]. Group 5: Future Vision and Commitment - The company aims to become a global "Big Pharma" over the next decade, focusing on innovation, deep internationalization, and comprehensive AI adoption as its core strategies [19][20]. - Fosun Pharma's mission remains to ensure every family enjoys health, reflecting its commitment to addressing clinical needs through continuous innovation [20].

Group 1 - Shanghai Fosun Pharmaceutical Group Co., Ltd. successfully issued the first private pharmaceutical industry medium to long-term technology innovation bond in China, with a scale of 1 billion RMB and a maturity of 2 years at a coupon rate of 2.70% [2] - The bond received enthusiastic subscriptions from various financial institutions, including bank wealth management, insurance, foreign banks, public funds, and securities firms [2] - The successful issuance of the technology innovation bond further consolidates Fosun Pharma's leading position among domestic innovative pharmaceutical companies and supports the company's high-quality development [3] Group 2 - Fosun Pharma has been driven by innovation for over 30 years, having approved 12 self-developed and licensed innovative drugs and biosimilars since 2019 [3] - The company has secured commercial rights for 8 innovative drugs in China, covering key treatment areas such as solid tumors, hematological tumors, and immune inflammation [3] - Fosun Pharma aims to deepen its innovation transformation and provide better and more accessible products and services for patients and clients, while creating sustainable value returns for shareholders [3]

Group 1 - Recently, Fosun Pharma successfully issued the first long-term technology innovation bond in the private pharmaceutical sector in China, with a scale of 1 billion RMB, a term of 2 years, and a coupon rate of 2.70% [1] - The bond received enthusiastic subscriptions from various financial institutions, including bank wealth management, insurance, foreign banks, public funds, and securities firms, indicating strong market support [1][2] - The funds raised will provide strong financial support for Fosun Pharma's layout in key technology innovation areas, accelerating the transformation and implementation of innovative results [1] Group 2 - The issuance of this technology innovation bond aligns with the central government's policies to support the healthy and high-quality development of the private economy, as emphasized in recent meetings and action plans [1][2] - Fosun Pharma has been focusing on innovation as its core development driver for over 30 years, having received approvals for 12 self-developed and licensed innovative drugs since 2019, covering critical treatment areas [3] - The company aims to deepen its innovation transformation and provide high-quality, accessible products and services to patients and customers, while creating sustainable value returns for shareholders [3]

Overview - Shanghai Fosun Pharmaceutical (Group) Co., Ltd. has initiated a Phase III clinical trial for its self-developed drug, Rumaine (generic name: Luwomeitini tablets), aimed at treating pediatric low-grade glioma in mainland China [1][2]. Drug Information and Research Status - Rumaine is an innovative small molecule chemical drug that acts as a selective inhibitor of MEK1/2 [1]. - As of July 9, 2025, the drug is in Phase III clinical trials for treating pediatric low-grade glioma and is also in Phase II trials for treating extra-cranial arteriovenous malformations and pediatric Langerhans cell histiocytosis in mainland China [2]. - The drug has been included in the breakthrough therapy program by the National Medical Products Administration for two indications: inoperable or residual/recurrent NF1-related plexiform neurofibromas in adult patients and pediatric Langerhans cell histiocytosis [2]. - Cumulative R&D investment in the drug reached approximately RMB 607 million (unaudited) as of May 2025 [2]. - According to IQVIA MIDAS™, global sales of MEK1/2 selective inhibitors are projected to be approximately USD 2.068 billion in 2024 [2].