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BD新玩法?百济神州9.5亿美元“变现”塔拉妥单抗海外收益
2 1 Shi Ji Jing Ji Bao Dao· 2025-08-26 11:00
根据协议条款,百济神州将获得8.85亿美元的首付款,并有权在12个月内出售剩余的收取特许权使用费 的权利,由此最高可获得6500万美元的额外付款。此外,百济神州将根据特许权使用费所占比例,享有 该产品年销售额超15亿美元的部分收入。 8月25日晚间,百济神州(纳斯达克代码:ONC;香港联交所代码:06160.HK;上交所代码: 688235.SH)公告与Royalty Pharma达成协议,向其出售就安进公司授权合作产品塔拉妥单抗(英文商品 名:IMDELLTRA ;通用名:tarlatamab)在中国以外的全球销售额收取特许权使用费的权利,交易金 额最高达9.5亿美元。 21世纪经济报道记者 韩利明 谈及此次交易模式,百济神州在公告中强调"不涉及任何知识产权权属的转让"。对此,不少业内观点解 读为是创新药企业BD(商务拓展)的"新路径",即此次合作并非将药物"全盘出售",而是通过"出 租"药物的商业化分红权益实现资金回笼。 高特佳投资集团副总经理王海蛟向21世纪经济报道分析指出,"这是企业获取现金流、补充流动性的一 种方式。当前中国创新药企的融资工具愈发多元化,已不仅限于股权融资与传统BD交易,还可通过分 ...
信达生物(01801):IO及ADC在研管线具备较大潜力,期待玛仕度肽上量
CSC SECURITIES (HK) LTD· 2025-07-24 08:28
Investment Rating - The report assigns a "Buy" rating for the company, indicating a potential upside in the stock price [7]. Core Insights - The company aims to become a leading international biopharmaceutical firm, with significant achievements in commercialization and a robust pipeline in oncology and other therapeutic areas [7]. - The company has 16 products approved for sale, with projected sales revenue of RMB 8.2 billion in 2024, reflecting a year-over-year growth of 44% [7]. - The company has achieved positive Non-IFRS profit and EBITDA for the first time, with figures of RMB 330 million and RMB 410 million respectively for 2024 [7]. - The company expects to maintain positive EBITDA in 2025 and aims to launch 20 commercialized products by 2027, targeting revenue of RMB 20 billion [7]. Summary by Sections Company Overview - The company operates in the pharmaceutical and biotechnology sector, with a current H-share price of HKD 88.00 and a target price of HKD 107 [4]. - The company has a market capitalization of RMB 65.35 billion and a price-to-book ratio of 10.99 [4]. Product Portfolio - The revenue breakdown shows that 87% comes from drug sales, 12% from licensed products, and 1% from R&D income [5]. Financial Projections - The company is projected to achieve net profits of RMB 373 million, RMB 1.43 billion, and RMB 2.40 billion for the years 2025, 2026, and 2027 respectively, with year-over-year growth rates of 282% and 68.4% [9]. - The earnings per share (EPS) are expected to be RMB 0.22, RMB 0.84, and RMB 1.41 for the same years [9]. Market Position and Competitive Advantage - The company is recognized for its innovative drug pipeline, particularly in immune-oncology (IO) and antibody-drug conjugates (ADC), with promising clinical results for its PD-1/IL-2 dual-target drug [7]. - The recent launch of the weight-loss drug, Ma Shidu Peptide, is expected to significantly contribute to revenue growth, showing a weight loss of 18.6% over 48 weeks, outperforming existing competitors [7].
Innovent Biologics Showcases "Dual Innovations" at Oncology R&D Day, Pioneering the Future of Cancer Treatment with Next-Generation IO and ADC Platforms
Prnewswire· 2025-06-30 04:04
Core Insights - Innovent is positioned as a leader in China's biopharmaceutical sector, particularly in oncology, with over 3 million cancer patients treated using its therapies [1] - The company is focusing on global innovation through a robust pipeline, aiming to advance at least five pipeline assets into MRCT Phase 3 trials by 2030 [1][5] - Innovent's strategy emphasizes dual innovation in next-generation immunotherapy (IO) and antibody-drug conjugates (ADC), targeting significant challenges in cancer treatment [2][3] R&D Strategy - Innovent's oncology pipeline includes nearly 10 next-generation molecules in global development, with multi-regional trials in the U.S., EU, and Asia [4] - The company is investing in R&D infrastructure, with hubs in Shanghai and San Francisco, and manufacturing capacity exceeding 140,000L [4] - Innovent Academy serves as the discovery engine, aiming to generate 6–8 novel molecules per year, focusing on next-gen IO and ADC [9] Pipeline Highlights - Key candidates include IBI363, a first-in-class PD-1/IL-2α-bias fusion protein, and IBI343, an innovative CLDN18.2 ADC, both showing significant survival benefits in clinical trials [5][6] - IBI363 has received two Breakthrough Therapy Designations from the NMPA CDE and two Fast Track Designations from the FDA, indicating its rapid advancement toward registrational development [7] - The pipeline also features IBI3001, IBI3003, and IBI3020, targeting various solid tumors with innovative mechanisms [6][13] Global Innovation and Market Position - Innovent is expanding its global footprint, with a vision to influence global oncology standards through its innovative therapies [10][11] - The company is recognized for its potential to lead in the next global oncology paradigm, driven by advancements in translational capabilities and patient-centric trial execution [11] - Innovent's commitment to high-quality, accessible cancer treatments positions it as a premier biopharmaceutical leader [15]