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中国生物制药(01177) - 公司秘书及授权代表之变更

2026-01-13 10:02
中國生物製藥有限公司(「本公司」)董事會(「董事會」)宣佈,自二零二六年一月十三日起: 陳先生確認與董事會並無分歧意見,亦無有關其辭任而須知會聯交所及本公司股東之事宜。 賴女士自二零二五年九月加入本公司,加入本公司之前,彼曾就職於普華永道中天會計師事務所、 里昂證券研究以及數家於聯交所上市之公司,在財務審計、資本市場、信息披露、企業管治及公司 秘書事務領域擁有逾十七年經驗。賴女士畢業於北京大學光華管理學院會計學專業,取得管理學學 士學位,並於香港大學取得工商管理碩士學位。彼為香港公司治理公會及英國特許公司治理公會特 許秘書、特許公司治理師以及會士。 1 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。 (於開曼群島註冊成立之有限公司) 網站:www.sinobiopharm.com (股份編號:1177) 公司秘書及授權代表之變更 謝其潤 香港,二零二六年一月十三日 於本公告日期,本公司董事會包括六位執行董事,即謝其潤女士、謝炳先生、鄭翔玲女士、謝承潤 ...
中国生物制药(01177) - 股份交易收购赫吉亚100%股权涉及根据一般授权发行代价股份

2026-01-13 09:40
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。 本公告僅供參考,並不構成收購、購買或認購本公司證券的邀請或要約,亦不在任何司法權區構成 任何投票或批准的招攬。 本公告並非旨在以直接或間接方式於或向美國或有關發佈、刊發或派發屬違法的司法權區派發。本 公告並不構成在美國或任何其他倘無根據當地證券法律登記或符合資格即屬違法的司法權區,要約 提呈出售任何證券或邀請作出購買任何證券的要約。倘無登記或獲適用豁免登記規定,證券不得在 美國提呈發售或出售。於美國公開發售任何證券將須以招股章程的方式進行,而招股章程須載有關 於提呈發售的公司、管理層以及財務報表的詳盡資料。本公司無意在美國公開發售證券。 (於開曼群島註冊成立之有限公司) 網站:www.sinobiopharm.com (股份編號:1177) 股份交易 收購赫吉亞100%股權 涉及根據一般授權發行代價股份 董事會欣然宣佈,於二零二六年一月十三日,本公司(透過買方)全資收購赫吉亞。買方(本公司一 間全資附屬 ...
瑞银:中国生物制药管理层对凝血因子VIIa入选国家医保目录感乐观 目标价12.2港元
Zhi Tong Cai Jing· 2026-01-13 09:23
Group 1 - UBS report indicates that China Biologic Products (01177) management requires more time to finalize guidance on the development of its out-licensing (BD) business for this year [1] - Expected data releases this year include Phase I clinical data for TQB3702 in blood cancer, Phase II clinical data for TQA3334, and Phase III clinical data for lanifibranor targeting metabolic-associated fatty liver disease [1] - The firm maintains a "Buy" rating on the company with a target price of HKD 12.2 [1] Group 2 - Management expresses optimism regarding the inclusion prospects of VIIa in the 2025 National Medical Insurance Drug List negotiations, as only three companies were selected [1] - Penpulimab has successfully entered the medical insurance directory for the first time; anlotinib has been approved for expansion to first-line treatment of soft tissue sarcoma without any price reduction, while Yilishu benefits from an expanded reimbursement scope [1]
瑞银:中国生物制药(01177)管理层对凝血因子VIIa入选国家医保目录感乐观 目标价12.2港元
智通财经网· 2026-01-13 09:19
Group 1 - UBS reports that China Biologic Products (01177) management indicates that more time is needed to determine the guidance for the external authorization (BD) business development this year [1] - The expected data results to be announced this year include Phase I clinical data for TQB3702 in blood cancer, Phase II clinical data for TQA3334, and Phase III clinical data for lanifibranor targeting metabolic-associated fatty liver disease [1] - UBS maintains a "Buy" rating for the company with a target price of HKD 12.2 [1] Group 2 - Regarding the 2025 National Medical Insurance Drug List negotiation results, management is optimistic about the inclusion prospects for VIIa, as only three companies were selected [1] - Penpulimab has successfully entered the medical insurance directory for the first time; Anlotinib has been approved for expansion to first-line treatment of soft tissue sarcoma without any price reduction, while Yilishu benefits from an expanded reimbursement scope [1]
港股中国生物制药一度涨超4%

Mei Ri Jing Ji Xin Wen· 2026-01-13 03:37
(文章来源:每日经济新闻) 每经AI快讯,中国生物制药(01177.HK)一度涨超4%,截至发稿涨3.5%,报7.09港元,成交额4.31亿港 元。 ...
中国生物制药午前涨近4% 美银证券重申“买入”评级
Xin Lang Cai Jing· 2026-01-13 03:33
中国生物制药(01177)盘中涨超4%,截至发稿,股价上涨3.50%,现报7.09港元,成交额4.39亿港元。 基于销售数据,美银证券微调其2026及2027年收入预测,目标价从9.4港元下调至8.3港元。此外,石药 集团因重点药品销售低迷,被维持"跑输大市"评级。 来源:新浪港股 报告显示,医院渠道销售额按年转降3.3%,零售渠道基本持平。中国生物制药产品表现分化,部分核 心产品销售额增长,但另一些显著下滑。 近日,美银证券发布报告指出,10月中国内地医药行业药品销售额按年下降3%,增速较9月大幅回落, 并重申对中国生物制药的"买入"评级。 ...
港股异动 | 中国生物制药(01177)涨超4% 管理层对VIIa入保前景表示乐观 药品为旗下正大天晴开发
智通财经网· 2026-01-13 03:24
Core Viewpoint - China Biologic Products (01177) has seen a stock increase of over 4%, currently trading at 7.09 HKD with a transaction volume of 431 million HKD, as reported by UBS [1] Group 1: Business Development - The management of China Biologic Products indicated that more time is needed to finalize the guidance for its out-licensing (BD) business for this year [1] - Key data results expected this year include Phase I clinical data for TQB3702 in blood cancer, Phase II clinical data for TQA3334, and Phase III clinical data for lanifibranor targeting metabolic-associated fatty liver disease [1] Group 2: Market Outlook - The management is optimistic about the inclusion prospects of VIIa in the 2025 National Medical Insurance Drug List negotiations, as only three companies are selected for inclusion [1] - Penpulimab has successfully entered the medical insurance list for the first time, while anlotinib has been approved for expansion to first-line treatment of soft tissue sarcoma without any price reduction [1] - Yilishu benefits from an expanded reimbursement scope [1] Group 3: Product Information - The VIIa product is the recombinant human coagulation factor VIIa N01 (brand name: Anqixin) developed by China Biologic Products' subsidiary, which received NMPA approval for market entry on July 3, 2025 [1] - This product is the first domestically produced recombinant human coagulation factor VIIa biological product, breaking the long-standing monopoly of imported products, improving drug accessibility for hemophilia patients, and reducing treatment costs [1]
中国生物制药涨超4% 管理层对VIIa入保前景表示乐观 药品为旗下正大天晴开发
Zhi Tong Cai Jing· 2026-01-13 03:24
Core Viewpoint - China Biologic Products (01177) has seen a stock increase of over 4%, currently trading at 7.09 HKD with a transaction volume of 431 million HKD. UBS reports that the management requires more time to finalize the guidance for the business development of external authorization (BD) this year [1] Group 1: Clinical Data and Product Development - The company is expected to announce clinical data results this year, including Phase I clinical data for TQB3702 in blood cancer, Phase II clinical data for TQA3334, and Phase III clinical data for lanifibranor targeting metabolic-associated fatty liver disease [1] - Management is optimistic about the inclusion prospects of VIIa in the 2025 National Medical Insurance Drug List negotiations, as only three companies have been selected for inclusion [1] Group 2: Recent Approvals and Market Impact - Penpulimab has successfully entered the medical insurance catalog for the first time, while anlotinib has been approved for expansion to first-line treatment of soft tissue sarcoma without any price reduction [1] - Yilishu benefits from an expanded reimbursement scope, enhancing its market accessibility [1] Group 3: Product Significance - The VIIa product, developed by the company's subsidiary, is the first domestically produced recombinant human coagulation factor VIIa (brand name: Anqixin), which received NMPA approval on July 3, 2025 [1] - This product breaks the long-standing monopoly of imported products, improving medication accessibility for hemophilia patients and reducing treatment costs [1]
中国生物制药高管连续增持,创新药接连报捷
Zheng Quan Shi Bao Wang· 2026-01-04 03:57
Group 1 - The core point of the news is that China Biologic Products (01177.HK) has seen significant insider buying from its executive director, demonstrating confidence in the company's long-term development [1] - Executive Vice President Xie Xin purchased 1 million shares at an average price of HKD 6.4068 per share, totaling approximately HKD 6.4068 million, increasing his holdings to 361 million shares, representing 1.92% of the company [1] - This marks Xie Xin's third purchase since July 2025, with previous purchases made at average prices of HKD 6.47 and HKD 7.36, indicating a total investment of over HKD 20 million in the past six months [1] Group 2 - The mid-year report for 2025 indicates that China Biologic Products' innovative transformation is showing significant results, with expectations that revenue from innovative products will exceed 50% of total revenue [2] - The company has achieved several milestones since December last year, including the approval of the breast cancer innovative drug Kemosil capsules, which is the world's first CDK2/4/6 inhibitor [2] - Other notable advancements include the clinical application approvals for the oral GLP-1 receptor agonist TQF3250 for weight loss by both the NMPA and FDA, and positive progress in the phase II clinical trial of the TYK2/JAK1 inhibitor TQH3906 for plaque psoriasis [2]
中国生物制药(01177) - 截至二零二五年十二月三十一日止月份的股份发行人的证券变动月报表

2026-01-02 02:09
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 截至月份: 2025年12月31日 狀態: 新提交 致:香港交易及結算所有限公司 公司名稱: 中國生物製藥有限公司 呈交日期: 2026年1月2日 I. 法定/註冊股本變動 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) | 01177 | 說明 | - | | | | | | | | | 法定/註冊股份數目 | | | 面值 | | 法定/註冊股本 | | | 上月底結存 | | 30,000,000,000 | | HKD | | 0.025 HKD | | 750,000,000 | | 增加 / 減少 (-) | | | 0 | | | HKD | | 0 | | 本月底結存 | | | 30,000,000,000 | HKD | | 0.025 HKD | | 750, ...