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创新转型获认可 复星医药成功发行10亿元中长期科技创新债券
Zheng Quan Ri Bao· 2025-08-15 05:13
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]
复星医药: 复星医药关于控股子公司药品临床试验进展的公告
Zheng Quan Zhi Xing· 2025-07-09 09:15
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].