格隆汇8月26日丨宜明昂科-B(01541.HK)公布中期业绩，截至2025年6月30日止六个月，收入为人民币 3800万元，较截至2024年6月30日止六个月的人民币10万元增加人民币3790万元，主要归因于根据公司 与Axion Bio, Inc.达成的授权及合作协议收取近期付款。 研发开支由截至2024年6月30日止六个月的人民币1.191亿元增加41.0%至截至2025年6月30日止六个月的 人民币1.68亿元，主要归因于(i)临床前及CMC开支增加人民币4340万元(主要由于临床试验使用的 IMM01、IMM2510及IMM0306的生产及CDMO开支增加)；(ii)临床试验开支增加人民币830万元(主要由 于IMM01及IMM2510的持续临床开发)；及(iii)薪金及相关福利费用因公司的临床团队不断扩大而增加 人民币490万元，与公司持续推进及扩大药物管线的研发工作相符合；部分被以股份为基础的付款减少 人民币670万元(由于截至2025年6月30日止六个月已归属的受限制股份数目减少)所抵销。 ...

公告称，收入增加主要归因于集团根据公司与Axion Bio,Inc.达成的授权及合作协议收取近期付款。 宜明昂科-B(01541)发布截至2025年6月30日止六个月中期业绩，收入3802.7万元(人民币，下同)，同比 增加49285.71%;研发开支1.68亿元，同比增加41.05%。 研发开支增加主要归因于(i)临床前及CMC开支增加4340万元(主要由于临床试验使用的IMM01、 IMM2510及IMM0306的生产及CDMO开支增加);(ii)临床试验开支增加830万元(主要由于IMM01及 IMM2510的持续临床开发);及(iii)薪金及相关福利费用因集团的临床团队不断扩大而增加490万元，与集 团持续推进及扩大药物管线的研发工作相符合;部分被以股份为基础的付款减少670万元(由于截至2025 年6月30日止六个月已归属的受限制股份数目减少)所抵销。 ...

研发开支增加主要归因于(i)临床前及CMC开支增加4340万元(主要由于临床试验使用的IMM01、 IMM2510及IMM0306的生产及CDMO开支增加);(ii)临床试验开支增加830万元(主要由于IMM01及 IMM2510的持续临床开发);及(iii)薪金及相关福利费用因集团的临床团队不断扩大而增加490万元，与集 团持续推进及扩大药物管线的研发工作相符合;部分被以股份为基础的付款减少670万元(由于截至2025 年6月30日止六个月已归属的受限制股份数目减少)所抵销。 智通财经APP讯，宜明昂科-B(01541)发布截至2025年6月30日止六个月中期业绩，收入3802.7万元(人民 币，下同)，同比增加49285.71%;研发开支1.68亿元，同比增加41.05%。 公告称，收入增加主要归因于集团根据公司与Axion Bio, Inc.达成的授权及合作协议收取近期付款。 ...

Investment Rating - The report rates the pharmaceutical and biotechnology industry as "stronger than the market" [1]. Core Insights - The pharmaceutical sector has outperformed the CSI 300 index, with a weekly increase of 2.95% compared to a decline of 1.75% for the index. The focus remains on innovative drugs, which continue to attract significant market interest [5][6]. - The SW Pharmaceutical Biotechnology Index has seen a cumulative increase of 22.96% year-to-date, while the Hang Seng Biotechnology Index has surged by 87.68% [2][13]. - The report highlights the ongoing trend of Chinese innovative drugs entering international markets, with significant upcoming scientific conferences expected to showcase new research and facilitate business development (BD) transactions [2][15]. Summary by Sections Market Review - The pharmaceutical sector has shown resilience, ranking first among 31 sectors during the week of July 28 to August 3, with notable performances from innovative drug companies [5][6]. - Key players like Hengrui and GSK have engaged in substantial collaborations, with a deal worth up to $12 billion [38][39]. Investment Strategy - The report suggests focusing on core sectors with potential for business development, particularly ADCs and PD-1 bispecific antibodies. Companies like Maiwei Biotech and Yiming Oncology are highlighted for their promising pipelines [15][17]. - The report emphasizes the importance of monitoring mid-year earnings reports from high-growth companies in the CXO and medical device sectors [15]. Company Highlights - **基石药业 (KeyStone Pharmaceuticals)**: Plans to present clinical data for its PD-1 tri-antibody CS2009 at the ESMO 2025 conference, which is expected to demonstrate superior efficacy compared to existing treatments [18][19]. - **维立志博 (Vilaizhibo)**: Successfully listed on the Hong Kong Stock Exchange, with its PD-L1/4-1BB bispecific antibody LBL-024 showing promising clinical results [26][30]. - **宜明昂科 (Yiming Oncology)**: Reported positive data for its PD-L1/VEGF bispecific antibody IMM2510 in treating non-small cell lung cancer, achieving an overall response rate of 62% [34][35]. - **中国生物制药 (China Biopharmaceutical)**: Anticipates receiving a $300 million milestone payment for its LM-299 project, indicating strong progress in its collaboration with Merck [36]. Industry Dynamics - The report notes that all sub-sectors within the pharmaceutical industry have outperformed the CSI 300 index, with chemical preparations and other biological products leading the gains [6]. - The innovative drug sector remains a focal point, with significant interest in the development of new therapies and collaborations with multinational corporations [2][40].

Company Overview - Yiming Biopharmaceutical Technology (01541.HK) was established in 2015 and listed on the Hong Kong main board in September 2023, focusing on "immune system activation" to develop innovative drugs that help the body's immune cells attack cancer cells [2] - Key products include IMM01 (activates the immune system to engulf cancer cells) and IMM2510 (a globally pioneering bispecific antibody drug that simultaneously inhibits tumor angiogenesis and activates immunity) [2] Product Pipeline - Currently, there are 6 products in Phase III clinical trials [3] Management and Shareholders - The founder and Chief Scientific Officer, Dr. Tian Wenzhi, holds approximately 17% of the shares and has over 30 years of experience in the biopharmaceutical industry, overseeing the company's overall strategy and clinical progression [5] - Major shareholders include Shanghai Zhangke Leading Investment (approximately 9%) and LAV Asset Management (approximately 6.8%), both of which have a strong focus on early-stage biopharmaceutical investments [6] Financial Performance - The company reported revenues of RMB 538,000 in 2022, with a net loss of RMB 402.894 million, and in 2023, revenues decreased to RMB 386,000 with a net loss of RMB 379.459 million [8][9] - In 2024, revenues are projected to increase significantly to RMB 74.149 million, driven by a licensing agreement with Axion Bio, which contributed approximately RMB 71.342 million [11] - The company has maintained high R&D investment, with expenditures of RMB 320 million in 2024, which is 4.4 times its revenue [11] Product Advantages - IMM2510 employs a dual-pathway immune strategy, combining innate and adaptive immunity, and has completed Phase I dose exploration with promising early data [16] - IMM0306, a CD47×CD20 bispecific fusion protein, has a high effective relief rate of 91%, outperforming competitors [17] Industry Trends - The global immuno-oncology market is expected to grow from approximately USD 126.5 billion in 2024 to about USD 271.1 billion by 2033, with a CAGR of 8.6% to 10.65% [18] - The market is driven by rising cancer incidence rates, with an estimated 20 million new cases in 2022, projected to increase to 35 million by 2050 [18] Competitive Landscape - The company avoids the highly competitive single-pathway PD-1 market and focuses on combination therapies targeting CD47 and CD20, which may qualify for orphan drug status and expedited approval [21] Valuation and Market Performance - The company's stock price has increased by 178.6% year-to-date, driven by significant R&D progress and market interest in the biopharmaceutical sector [24] - Revenue projections for 2025-2027 are estimated at RMB 201 million, RMB 122 million, and RMB 312 million, respectively, with a target market value of HKD 8.915 billion [24]

Core Insights - The PD-1/VEGF dual antibody is currently a hot topic in innovative drug development, with significant collaborations and financial transactions highlighting its potential [1][2][3] Group 1: Industry Dynamics - Chinese biotech companies are emerging as key players in the global PD-(L)1/VEGF dual antibody development race, demonstrating advanced research progress and achieving international recognition through high-value business development (BD) deals [2][3] - Major collaborations include 12.5 billion USD upfront payment and 60.5 billion USD total deal value between 3SBio and Pfizer for SSGJ-707, and BioNTech's 15 billion USD upfront payment for BNT327 licensed to BMS, totaling over 90 billion USD [1][2] Group 2: Clinical Developments - The PD-(L)1/VEGF target gained traction after Kangfang Biotech's AK112 outperformed the benchmark drug, Pembrolizumab (K drug), in head-to-head trials, leading to increased interest from multinational corporations (MNCs) [3][4] - AK112 demonstrated a higher objective response rate (ORR) of 50% compared to K drug's 38.5% and a disease control rate (DCR) of 89.9% versus 70.5% in late-stage non-small cell lung cancer (NSCLC) trials [4][6] Group 3: Competitive Landscape - The success of AK112 has intensified competition among MNCs, with companies eager to capitalize on the potential of PD-(L)1/VEGF dual antibodies, as evidenced by Pfizer's strategic investments [9][10] - As of May 2025, there are 14 PD-(L)1/VEGF dual antibodies in clinical stages globally, with half originating from Chinese biotech firms, indicating a robust pipeline and potential for further BD opportunities [15][24] Group 4: Future Prospects - Companies like Junshi Biosciences, I-Mab, and Hualan Biological Engineering are actively pursuing PD-(L)1/VEGF dual antibodies, with significant investments and clinical trials underway [15][20][22] - The shift from merely imitating existing drugs to innovating new targets and technologies marks a significant evolution in the Chinese pharmaceutical industry, enhancing its international competitiveness [24][25]

Investment Rating - The report maintains an "Overweight" rating for the pharmaceutical and biotechnology sector [5]. Core Insights - The PD-1 (PD-L1)/VEGF dual antibody concept is gaining significant attention, with Chinese innovative pharmaceutical companies leading the research and development efforts [2][20]. - The global market for dual antibodies is projected to exceed $80 billion by 2030, with PD-1 (PD-L1)/VEGF drugs expected to challenge the traditional PD-1/PD-L1 drugs in cancer treatment [20][21]. - The report highlights the importance of clinical data barriers and international expansion for companies in this sector, suggesting that these factors will create differentiated investment opportunities [3][26]. Summary by Sections Market Review - The pharmaceutical and biotechnology index rose by 2.21%, outperforming the CSI 300 index by 3.30 percentage points and the ChiNext index by 2.00 percentage points, ranking second among 31 sub-industries [11][12]. Clinical Progress - Notable advancements include the IND applications for BG-60366 by BeiGene and RFUS-949 by Renfu Pharmaceutical, as well as ongoing clinical trials for various drugs by companies like Hengrui Medicine and Stone Pharmaceutical [29][30]. Key Developments - The report notes that 14 PD-1 (PD-L1)/VEGF products are currently in clinical stages, all associated with Chinese companies, with the fastest progress seen in Ivonescimab by Kangfang Biotech, which has been approved in China [21][22]. Investment Strategy - The report emphasizes a structural selection of investment opportunities based on payment willingness and ability, focusing on three payment channels: hospital payments, out-of-pocket payments, and overseas payments [4][26]. - Recommended companies include Hengrui Medicine, Mindray Medical, United Imaging Healthcare, and Yuyue Medical [4]. Company Announcements - Recent announcements include various companies receiving approvals for new drugs and medical devices, indicating ongoing innovation and regulatory progress within the sector [28][29].

Core Insights - Bristol-Myers Squibb (BMS) acquired BioNTech's PD-L1/VEGF dual antibody BNT327 for $9 billion, highlighting the increasing interest in Chinese biotech firms and their innovative drug pipelines [1][2] - The rapid financial success of BioNTech, which earned over $8 billion from the initial $55 million licensing deal with Chinese firm Pumice Biologics, raises questions about the pricing strategies of Chinese pharmaceutical companies in the global market [1][2][3] - The trend of multinational corporations (MNCs) aggressively acquiring Chinese dual antibodies is reshaping the global landscape of innovative drugs, with significant deals such as the $6.05 billion agreement between 3SBio and Pfizer [1][4] Group 1: Major Transactions - BMS's deal with BioNTech includes a $1.5 billion upfront payment, a record for oncology licensing agreements, along with additional milestone payments totaling $76 billion [2] - 3SBio's licensing of its PD-1/VEGF dual antibody SSGJ-707 to Pfizer for $6.05 billion, with an upfront payment of $1.25 billion, sets a new record for domestic innovative drug licensing [4][5] - Other notable transactions include Merck's $3.3 billion investment in LianBio and the anticipated $5 billion deal involving Shijiazhuang Yiling Pharmaceutical [5][6] Group 2: Market Dynamics - The surge in MNCs acquiring Chinese dual antibodies is driven by the expiration of patents for existing blockbuster drugs and the need for new products [6][7] - Chinese innovative drug companies benefit from lower development costs and a large patient pool, making them attractive targets for MNCs seeking to enhance their product pipelines [6][7] - The total value of outbound licensing deals for Chinese innovative drugs reached $45.5 billion since early 2025, with 42% of high-value projects coming from China [5][6] Group 3: Future Outlook - The ongoing trend of MNCs partnering with Chinese biotech firms is expected to bolster the confidence of domestic companies in pursuing research and development [7][8] - The ability of Chinese innovative drug companies to negotiate higher prices in licensing deals will depend on their negotiation skills and market positioning [8] - The need for a "pricing power revolution" in the Chinese pharmaceutical industry is emphasized, as companies face challenges from rising R&D costs and stringent domestic pricing policies [9]

Core Insights - Chinese biotechnology companies are leading the development of PD-L1/VEGF bispecific antibody drugs, with BMS partnering with BioNTech to commercialize a next-generation cancer immunotherapy [1][5] - BioNTech acquired the drug BNT327 from a Chinese company for less than $1 billion, and within six months, it was sold for over $11 billion [1][3] Group 1: Company Developments - BMS plans to invest up to $11.1 billion in collaboration with BioNTech to develop and commercialize BNT327, a bispecific antibody targeting PD-L1 and VEGF-A for various solid tumors [1][4] - BNT327 is currently undergoing clinical trials as a first-line treatment for extensive-stage small cell lung cancer and non-small cell lung cancer, with over 1,000 patients treated so far [4] Group 2: Market Impact - The announcement of the BMS and BioNTech deal led to a more than 20% increase in BioNTech's stock price and a nearly 30% rise in Instil Bio's stock price, indicating strong market interest in PD-L1/VEGF bispecific antibodies [5] - PD-L1/VEGF bispecific antibodies are becoming a hot research area in the pharmaceutical industry, with potential to replace Merck's Keytruda, which is projected to generate $29.5 billion in sales for the fiscal year 2024 [5] Group 3: Clinical Data and Collaborations - Recent clinical trial results from Kangfang Biotech and Summit Therapeutics showed that their PD-1/VEGF bispecific antibody, ivonescimab, reduced the risk of disease progression or death by 48% in previously treated patients with EGFR-mutant non-squamous non-small cell lung cancer [5] - Pfizer announced a collaboration with China's 3SBio for the PD-1/VEGF bispecific antibody SSGJ-707, with an upfront payment of $1.25 billion and potential milestone payments of up to $4.8 billion [6]

Group 1 - The stock of I-Mab (01541) increased by over 10%, reaching HKD 7.66 with a trading volume of HKD 40.02 million [1] - I-Mab announced the approval of its clinical trial application for Tazlestobart (IMM27M) in combination with Osimertinib for EGFR-mutant locally advanced or metastatic non-squamous non-small cell lung cancer by the National Medical Products Administration (NMPA) [1] - The company received a second payment of USD 5 million from Axion Bio, bringing the total amount received for the collaboration on IMM2510 and IMM27M to USD 20 million [1] Group 2 - Guoyuan International highlighted I-Mab as a research-driven biotechnology company capable of systematically utilizing both innate and adaptive immunity [2] - I-Mab is developing two CD47×CD20 bispecific antibodies/fusion proteins, with IMM0306 being the first to enter clinical trials, showing an overall response rate (ORR) of 90.9% and a complete response (CR) of 27.3% in an Ib trial with 11 patients [2] - Clinical trials for autoimmune diseases are currently in the Ib phase, with the SLE trial enrolling six patients in the second dose group, showing promising response rates, and data is expected to be released mid-year [2]