PD1/VEGF双抗

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创新药行业专题研究报告:创新突破,出海拓疆
Soochow Securities· 2025-06-05 01:16
Investment Rating - The report rates the innovative drug industry positively, indicating a significant growth potential and favorable market conditions for investment. Core Insights - The year 2025 is projected to be the starting point for at least three years of favorable market conditions for innovative drugs, driven by several key factors including high upfront payments for collaborations and improved domestic clinical environments [4]. - The Chinese innovative drug market is expected to experience rapid growth, with a projected market size of nearly 550 billion RMB in 2024 and an estimated CAGR of 24.1%, potentially exceeding 20 trillion RMB by 2030 [4][10]. - The research and development capabilities of Chinese companies have significantly improved, with a notable increase in the number of original FIC innovative drugs, positioning China as a global leader in certain therapeutic areas [4][27]. - The number and value of license-out transactions for Chinese innovative drugs have reached new highs, with 94 transactions in 2024 totaling 51.9 billion USD, reflecting a 26% year-on-year increase [4][46]. - The overall revenue of innovative drug companies is steadily increasing, with A-share companies projected to grow from 30.07 billion RMB in 2018 to 62.8 billion RMB in 2024, indicating a transition from high investment phases to profitability [4][18]. Summary by Sections 1. Market Outlook - The innovative drug market in China is set for explosive growth, with a total market size projected to reach 20 trillion RMB by 2030, representing a 264% increase from 2024 [10][4]. - The domestic innovative drug market is currently only 3% of the global market, indicating substantial growth potential [10]. 2. R&D Strength - Chinese companies have made significant advancements in R&D, with 41% of global innovative drug targets covered by domestic firms [27]. - The number of original FIC innovative drugs from Chinese companies surpassed that of Europe in 2021, ranking second globally [27]. 3. License-Out Transactions - The license-out transactions for Chinese innovative drugs have seen a remarkable increase, with 94 transactions in 2024 and a total transaction value of 51.9 billion USD [46][41]. - The trend of license-out transactions is expected to continue growing, with a projected total of 2.659 billion USD by 2030 [10]. 4. Revenue Growth - A-share innovative drug companies are expected to see their revenues grow significantly, with a projected increase to 62.8 billion RMB by 2024 [18]. - The overall profitability of innovative drug companies is improving, with several companies expected to turn profitable by 2025 and 2026 [4]. 5. Technological Advancements - The report highlights the emergence of advanced therapies such as ADCs and dual-target antibodies, suggesting a focus on high-tech innovations in the industry [4]. - The ASCO conference showcased a record number of presentations from Chinese companies, indicating the growing influence of Chinese innovations in global markets [4].
PD-1/VEGF的大额对外授权对FIC药企的影响
青侨阳光投资交流· 2025-05-20 07:37
Group 1 - The core viewpoint of the article emphasizes the significant potential of China's innovative drug industry, particularly highlighted by the recent large-scale licensing deal involving innovative drugs [1] - The innovative drug sector is characterized by a "bet first, collapse later" nature, making it suitable to view through a "cycle" perspective, where the most attractive aspect is the value escalation cycle of a technology or product transitioning from obscurity to a major market player [1][2] - The value escalation cycle for PD1/CTLA4 and PD1/VEGF dual antibodies began around 2020/2021, with expectations that this cycle will continue at least until 2027/2028, barring any major setbacks [2] Group 2 - The comparison between Sanofi's 707 and Ivosidenib indicates that while there may be some local improvements, it does not significantly differentiate itself enough to disrupt the value escalation cycle of Ivosidenib [4] - The introduction of Sanofi's 707 may have short-term negative impacts on the original drug companies in Hong Kong, as it reduces the potential acquisition interest from partners like SUMMIT, but long-term effects may be limited [5][6] Group 3 - The original drug companies in Hong Kong are expected to see value escalation primarily through three phases, with the current phase being the second stage that has been active for 4-5 years and is projected to continue for another 2-3 years [7][8] - The market's perception of the potential value of Ivosidenib in various cancers appears to be underappreciated, with estimates suggesting that its overseas licensing could support a market value of approximately 320-480 billion HKD for the licensing party [8][9] Group 4 - The future value expansion for companies hinges on their ability to ignite the "third stage rocket," which involves developing universally applicable therapies that can enhance the efficacy of PD1 dual antibodies [10][11] - Companies are already pursuing clinical trials for TROP2*NECTIN4 dual antibody ADCs and mRNA tumor vaccines, indicating a proactive approach to maintaining value escalation in the face of potential market shifts [11][13]