格隆汇8月11日丨云顶新耀(01952.HK)公布，谨定于2025年8月28日(星期四)举行董事会会议，以考虑及 通过集团截至2025年6月30日止六个月的中期业绩，以及处理其他事项。 ...

於本公告日期，董事會包括主席兼執行董事傅唯先生，執行董事羅永慶先生及何穎先生，非執行 董事曹基哲先生及馮洪剛先生，以及獨立非執行董事徐海音女士、李軼梵先生及蔣世東先生。 （於開曼群島註冊成立的有限公司） （股份代號：1952） Everest Medicines Limited 雲 頂 新 耀 有 限 公 司 董事會會議召開日期 雲頂新耀有限公司（「本公司」及其附屬公司「本集團」）董事會（「董事會」）茲通告謹 定於2025年8月28日（ 星期四 ）舉行董事會會議，以考慮及通過本集團截至2025年 6月30日止六個月的中期業績，以及處理其他事項。 承董事會命 雲頂新耀有限公司 主席兼執行董事 傅唯 香港，2025年8月11日 香港交易及結算所有限公司及香港聯合交易所有限公司對本公告的內容概不負責，對其準確性或 完整性亦不發表任何聲明，並明確表示，概不對因本公告全部或任何部份內容而產生或因倚賴該 等內容而引致的任何損失承擔任何責任。 ...

Group 1 - The core point of the article highlights the performance of Ping An Medical Health Mixed C Fund, which has a latest net value of 2.7815 yuan and has experienced a weekly return of -3.05%, a three-month return of 37.06%, and a year-to-date return of 79.66% [1] - The fund was established on November 28, 2023, and as of June 30, 2025, it has a total scale of 1.216 billion yuan [1] - The top ten stock holdings of the fund include companies such as CloudTop New Medicine, Innovent Biologics, and BeiGene, with the top ten holdings accounting for a total of 75.91% of the portfolio [1]

Core Viewpoint - The recent pullback in the innovative drug sector does not indicate a peak, as the underlying logic differs from previous market cycles, particularly the 2021 bubble [2][3]. Group 1: Current Market Conditions - The current rise in innovative drugs is supported by strong fundamentals, contrasting with the previous bubble driven by capital [4][5]. - Key drivers include the ability to generate revenue from overseas markets, gradual improvement in domestic drug consumption capacity, favorable policy changes, and advancements in technology [5][6][7]. - The Chinese market is expected to see a significant increase in the approval speed for innovative drugs, with the average approval time reduced from 24 months to 12 months [6]. Group 2: Investment Opportunities - The innovative drug market is likely to experience a long-term trend supported by various factors, including engineering talent, policy benefits, technological breakthroughs, and capital support [7]. - Companies in the sector face challenges in realizing their pipeline values, necessitating careful evaluation of current market valuations against potential future values [8][11]. - The market has shifted from negative expectations to normal expectations, leading to substantial price increases for many companies that were previously undervalued [9][10]. Group 3: Specific Company Analysis - For instance, He Yu Pharmaceutical has a market cap of approximately 70 billion HKD, with cash reserves of 23 billion RMB and pipeline values potentially exceeding 40 billion RMB [12][14]. - The company's lead pipeline candidate, Pimicotinib, has high market expectations, with projected peak sales exceeding 2 billion USD [12][14]. - Other companies in the sector exhibit similar characteristics, where short-term price increases may obscure the true intrinsic value of their businesses [17]. Group 4: Future Trends and Strategies - The market is expected to transition from a broad-based rally to a more differentiated performance, emphasizing the importance of identifying companies with strong fundamentals [18]. - Business Development (BD) will continue to be a critical factor, with companies focusing on reliable technologies and partnerships to drive growth [18][19]. - Pre-commercial companies are also seen as attractive investments, as their valuations can significantly increase upon achieving commercialization milestones [23][24]. Group 5: Industry Outlook - The Chinese innovative drug industry is undergoing a critical transformation, with improved R&D capabilities and capital efficiency, comparable to strong sectors like photovoltaics and new energy [25].

Core Insights - The article highlights the significant progress made by the Hong Kong-based innovative pharmaceutical company, YunTing New Medicine, with its drug, Naisufang® (Budesonide Enteric-Coated Capsules), which is the first and only fully approved treatment for IgA nephropathy [1][6] - The drug has received approval for a new indication in Taiwan, allowing it to be used for all adult patients at risk of disease progression, thus expanding its patient base and market potential [1][5] Group 1: Market Potential and Demand - IgA nephropathy is the most common primary glomerular disease globally, with a notably higher prevalence in Asian populations, where the risk of progression to end-stage renal disease is 56% higher compared to other populations [2] - In China, there are over 5 million patients with IgA nephropathy, with more than 100,000 new diagnoses each year, indicating a substantial market demand for effective treatments [2] - The approval of Naisufang® is expected to generate sales of 1 billion yuan in its first full year post-launch, reflecting its strong market potential [1][6] Group 2: Clinical and Regulatory Advancements - Naisufang® has been recognized as a breakthrough therapy by the Chinese National Medical Products Administration (NMPA), filling a significant gap in the treatment of IgA nephropathy [2][4] - The drug's unique mechanism of action, which targets gut mucosal immunity and reduces the production of pathogenic IgA1, has been validated through clinical studies, demonstrating a 50% reduction in kidney function decline [4] - The drug has received dual recommendations from both domestic and international guidelines, solidifying its position as a first-line treatment for IgA nephropathy [4] Group 3: Supply and Production Capacity - The approval for the expansion of Naisufang® production capacity was granted in August, addressing the urgent need to meet the growing market demand [3] - The expansion will ensure a steady supply of the drug across China and the broader Asian region, alleviating the unmet clinical needs for IgA nephropathy treatments [3] Group 4: Commercialization and Market Strategy - YunTing New Medicine has established an efficient commercialization framework, covering over 80% of potential hospitals in mainland China, benefiting more than 20,000 patients [6] - The drug's comprehensive approval across multiple regulatory bodies, including the NMPA, FDA, and EMA, enhances its market accessibility and patient coverage in Asia [6] - Analysts predict that Naisufang® could reach peak sales of 5 billion yuan, indicating its potential as a blockbuster product in the nephrology market [6]

股份發行人及根據《上市規則》第十九B章上市的香港預託證券發行人的證券變動月報表 | | | 致：香港交易及結算所有限公司 公司名稱: 雲頂新耀有限公司 呈交日期: 2025年8月6日 FF301 II. 已發行股份及/或庫存股份變動 | 1. 股份分類 | 普通股 | 股份類別 | 不適用 | | 於香港聯交所上市 (註1) | 是 | | | --- | --- | --- | --- | --- | --- | --- | --- | | 證券代號 (如上市) | 01952 | 說明 | 普通股 | | | | | | | | 已發行股份（不包括庫存股份）數目 | | 庫存股份數目 | | 已發行股份總數 | | | 上月底結存 | | | 327,713,384 | | 0 | | 327,713,384 | | 增加 / 減少 (-) | | | 645,659 | | 0 | | | | 本月底結存 | | | 328,359,043 | | 0 | | 328,359,043 | 第 2 頁 共 10 頁 v 1.1.1 I. 法定/註冊股本變動 | 1. 股份分類 | 普通股 | 股份類別 | ...

Core Insights - Yunding Xinyao's core product, Nefikang, has received full approval from Taiwan's drug regulatory authority, removing previous conditions related to clinical efficacy, thus solidifying its position as a first-line treatment for IgA nephropathy in Asia [1][2] - The expansion application for Nefikang's production capacity has been approved by China's National Medical Products Administration (NMPA), enabling the company to meet the growing clinical demand in China and Asia more efficiently [1][3] - Nefikang is the first non-oncology drug in China to be included in the breakthrough therapy category, filling a significant treatment gap for IgA nephropathy [2][3] Market Demand and Clinical Need - IgA nephropathy is the most common primary glomerular disease globally, with a higher progression risk to end-stage renal disease in Asian populations, which is 56% higher than other groups [2] - There are over 5 million patients in China with more than 100,000 new diagnoses annually, highlighting the urgent need for effective treatment options [2] - Nefikang's unique mechanism targets the underlying cause of IgA nephropathy, making it the only drug recommended by both international and domestic guidelines for this condition [2][3] Commercialization and Market Penetration - The company has established an efficient commercialization system, covering over 80% of potential hospitals in mainland China, benefiting more than 20,000 patients [4] - Sales projections for Nefikang suggest a peak potential of 5 billion yuan, indicating its potential as a significant product in the nephrology market [4] - The approval and market entry of Nefikang are expected to drive long-term growth for Yunding Xinyao, enhancing patient accessibility and coverage in key Asian markets [3][4]

Core Viewpoint - Genting Yongying (01952) has seen a stock price increase of over 3%, currently trading at 72.05 HKD with a transaction volume of 231 million HKD, following its strategic investment in Tianjing Bio [1] Group 1: Strategic Investment - Genting Yongying participated in Tianjing Bio's capital increase, acquiring new shares at a price of 1.95 USD per ADS, totaling approximately 30.9 million USD, making it the largest single shareholder of Tianjing Bio [1] - This strategic investment allows Genting Yongying to leverage Tianjing Bio's differentiated 4-1BB platform, dual antibody pipeline, and overseas clinical translation capabilities, creating synergies with its existing mRNA tumor vaccine portfolio [1] Group 2: Tianjing Bio's Pipeline - Tianjing Bio has a differentiated pipeline for tumor-targeted/immunotherapy, including Givastomig (Claudin18.2/4-1BB dual antibody) and Ragistomig (PD-L1/4-1BB dual antibody) [1] - Givastomig is currently being explored in first-line gastric cancer treatment in combination with O drug and chemotherapy, showing data superior to current first-line gastric cancer standard therapies in a Phase Ib study in the U.S. [1] - Ragistomig features a unique molecular design that binds PD-L1 only in the tumor microenvironment and activates 4-1BB, with Phase I data indicating an overall response rate (ORR) and disease control rate (DCR) superior to competing products targeting the same pathway [1]

Core Viewpoint - CloudTop New Horizon (01952) has increased by over 3%, currently trading at 72.05 HKD with a transaction volume of 231 million HKD, following its strategic investment in Tianjing Bio [1] Group 1: Strategic Investment - CloudTop New Horizon has participated in Tianjing Bio's capital increase, acquiring new shares at a price of 1.95 USD per ADS, totaling approximately 30.9 million USD, making it the largest single shareholder of Tianjing Bio [1] - The investment is expected to leverage Tianjing's differentiated 4-1BB platform, dual antibody pipeline, and overseas clinical translation capabilities, creating synergies with CloudTop's existing mRNA tumor vaccine portfolio [1] Group 2: Product Pipeline - Tianjing Bio possesses a differentiated pipeline of tumor-targeted/immunotherapies, including Givastomig (Claudin18.2/4-1BB dual antibody) and Ragistomig (PD-L1/4-1BB dual antibody) [1] - Givastomig is currently being explored in first-line gastric cancer treatment in combination with O drug and chemotherapy, showing superior data compared to current standard therapies in the U.S. Phase Ib study [1] - Ragistomig features a unique molecular design that binds PD-L1 only in the tumor microenvironment and activates 4-1BB, with Phase I data indicating better ORR and DCR compared to competing products targeting the same pathway [1]

Core Viewpoint - CloudTop New Horizon (01952) has seen a stock increase of over 3%, currently trading at 72.05 HKD with a transaction volume of 231 million HKD, following its strategic investment in Tianjing Bio [1] Group 1: Strategic Investment - CloudTop New Horizon has participated in Tianjing Bio's capital increase, acquiring new shares at a price of 1.95 USD per ADS, totaling approximately 30.9 million USD, making it the largest single shareholder [1] - This strategic investment allows CloudTop New Horizon to leverage Tianjing's differentiated 4-1BB platform, dual antibody pipeline, and overseas clinical translation capabilities, creating synergies with its existing mRNA tumor vaccine portfolio [1] Group 2: Tianjing Bio's Pipeline - Tianjing Bio possesses a differentiated pipeline of tumor-targeted/immunotherapies, including Givastomig (Claudin18.2/4-1BB dual antibody) and Ragistomig (PD-L1/4-1BB dual antibody) [1] - Givastomig is currently being explored in first-line gastric cancer treatment in combination with O drug and chemotherapy, showing superior data compared to current standard therapies in the U.S. Phase Ib study [1] - Ragistomig features a unique molecular design that selectively binds to PD-L1 in the tumor microenvironment and activates 4-1BB, with Phase I data indicating better overall response rate (ORR) and disease control rate (DCR) compared to competing products targeting the same pathway [1]