Group 1 - UBS report indicates that the management of China Biopharmaceutical requires more time to finalize the guidance for its out-licensing (BD) business development this year [1] - Management is optimistic about the inclusion prospects of coagulation factor VIIa in the 2025 National Medical Insurance Drug List negotiations [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] Group 2 - UBS currently assigns a "Buy" rating to the company with a target price of HKD 12.2 [1]

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]

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]

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]

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]

Core Insights - Akeso, Inc. reported record commercial sales in China and significant global advancements in its oncology and autoimmune pipelines for the first half of 2025, driven by its "IO 2.0 + ADC 2.0" strategy [2][11][34] - The company has established itself as a leader in immuno-oncology bispecific antibodies, particularly with cadonilimab and ivonescimab, which are being evaluated in numerous global clinical trials [5][6][9][22] - Akeso's non-oncology portfolio is also expanding, with recent product launches and ongoing developments in autoimmune diseases, contributing to overall growth [10][31][36] Financial Performance - Total commercial sales increased by 49.20%, from RMB 939.4 million in the first half of 2024 to RMB 1,401.6 million in the first half of 2025, reflecting robust market penetration [11] - Research and development expenses for the same period were RMB 731.2 million, with total cash and equivalents amounting to RMB 7,138.4 million as of June 30, 2025 [12] Oncology Pipeline - Ivonescimab and cadonilimab are being evaluated in 23 registrational/Phase III trials and over 20 Phase II studies globally, with ivonescimab demonstrating statistically significant overall survival benefits in its trials [6][8][18] - Cadonilimab has received approvals for multiple indications, including first-line treatments for cervical and gastric cancers, addressing significant unmet needs in immunotherapy [22][23][25] Non-Oncology Pipeline - The company has launched ebdarokimab and ebronucimab, with upcoming launches for gumokimab and manfidokimab, enhancing its competitive position in the autoimmune sector [10][31][35] - Akeso's innovative candidates targeting neurological diseases and other chronic conditions are also progressing through development [32][36] Strategic Initiatives - Akeso is advancing a next-generation pipeline of bispecific ADCs and dual-payload ADCs, aiming to redefine the oncology treatment landscape [27][29] - The company is open to strategic collaborations to enhance its global reach and maximize therapeutic value [26]