Core Viewpoint - Rongchang Biopharma has signed an exclusive licensing agreement with AbbVie for RC148, granting AbbVie exclusive rights for development, production, and commercialization outside Greater China [1] Group 1: Financial Aspects - Upon the agreement's effectiveness, Rongchang Biopharma will receive an upfront payment of $650 million [1] - The company is eligible for up to $4.95 billion in milestone payments related to development, regulatory, and commercialization [1] - Additionally, the company will receive a tiered royalty on net sales outside Greater China [1] Group 2: Strategic Implications - This licensing deal is expected to accelerate the global development and commercialization of RC148 [1] - The agreement is anticipated to enhance the company's brand value and international influence [1] Group 3: Risks and Uncertainties - There is uncertainty regarding the final payment amounts due to the inherent risks associated with innovative pharmaceuticals [1]

Core Viewpoint - The collaboration between AbbVie and Rongchang Biologics marks a significant shift in the global oncology treatment landscape, highlighting the trend of Chinese innovative drug companies partnering with multinational giants for drug development and commercialization [1][2]. Group 1: Collaboration Details - AbbVie and Rongchang Biologics signed an exclusive licensing agreement for the development, production, and commercialization of RC148, a bispecific antibody targeting PD-1 and VEGF [1]. - Rongchang Biologics will receive an upfront payment of $650 million and is eligible for up to $4.95 billion in milestone payments, along with a tiered royalty on net sales outside Greater China [1][2]. Group 2: Market Implications - This deal exemplifies the "China innovation + global market" model, allowing Rongchang Biologics to secure cash flow and accelerate clinical trials for RC148 while focusing on the Chinese market [2]. - AbbVie aims to enhance its product portfolio in immuno-oncology, particularly in the emerging PD-1/VEGF bispecific antibody space, which could synergize with existing antibody-drug conjugates (ADCs) and immuno-oncology (IO) drugs [2]. Group 3: Competitive Landscape - The PD-1/VEGF bispecific antibody represents a new class of cancer therapies that may overcome tumor resistance mechanisms by simultaneously blocking PD-1 and VEGF [3][5]. - Chinese companies are leading in this field, with notable products like Ak112/Ivonescimab and SSGJ707 entering clinical trials, indicating a competitive landscape for PD-1/VEGF bispecific antibodies [3][4]. Group 4: Industry Trends - The surge in business development (BD) transactions in the PD-1/VEGF bispecific antibody sector reflects increasing interest from multinational pharmaceutical companies in Chinese innovative drug assets [6]. - In 2025, the total value of Chinese innovative drug licensing transactions exceeded $130 billion, surpassing the U.S. for the first time, indicating a significant shift in the global pharmaceutical landscape [7][8]. Group 5: Future Outlook - The increasing recognition of Chinese innovative drugs is attributed to their rapid development and the ability to meet unmet clinical needs, enhancing their bargaining power in international collaborations [8][9]. - The industry is witnessing a transition from following to leading in drug innovation, with a clear direction for the future of Chinese pharmaceutical development [10].

1月13日盘中科创板股荣昌生物涨停，截至11:26，股价报114.46元，成交16.92亿元，换手率9.43%，振 幅10.97%。 科创板个股中，截至发稿上涨的共有238只，涨幅在10%以上的共有11只，除荣昌生物之外，涨停的还 有光云科技、近岸蛋白等，下跌的有360只，跌幅较大的有国科军工、江航装备、禾信仪器，分别下跌 11.42%、11.07%、9.98%。 资金面上，荣昌生物上一交易日主力资金净流出851.19万元，近5日净流入8670.16万元。 融资融券数据显示，该股最新（1月12日）两融余额为7.58亿元，其中，融资余额为7.56亿元，较上一个 交易日增加146.99万元，增幅为0.19%；融券余额为196.12万元，较上一个交易日减少4.33万元，降幅为 2.16%。近10日两融余额合计减少4711.95万元，降幅为5.85%，其间融资余额下降6.02%，融券余额增长 195.64%。 （文章来源：证券时报网） ...

Group 1 - The A-share market experienced fluctuations with the Shanghai Composite Index showing volatility, while trading volume exceeded 1.8 trillion yuan, indicating sustained active trading [1] - The innovative drug sector saw significant strength, with the Science and Technology Innovation Drug ETF Huatai (589120) surging over 3% as funds continued to flow into it for two consecutive days, driven by optimism around "BD going global + AI healthcare + brain-computer interfaces" [1] - The top ten constituent stocks of the Huatai ETF include companies like BeiGene (688235) and Junshi Biosciences (688180), with Rongchang Biopharmaceuticals (688331) leading with a 17.29% increase [1][5] Group 2 - Rongchang Biopharmaceuticals announced a licensing agreement with AbbVie for RC148, which includes a $650 million upfront payment and potential milestone payments up to $4.95 billion, along with double-digit royalties on net sales outside Greater China [1][2] - The transaction size of the upfront payment ranks among the top ten for domestic innovative drug companies going global, indicating the potential of RC148 in the global market [2] - The trend in the industry is shifting from "early licensing" to "deep binding" partnerships, with companies like Hengrui Medicine and Qianxin Biopharmaceuticals actively engaging in new cooperative models that share risks and long-term benefits [4][6] Group 3 - The innovative drug sector is expected to enter a phase of significant growth, with a focus on the lifecycle of BD transactions, which includes achieving overseas clinical validation and profit-sharing from sales [3][4] - The market anticipates a busy period for BD transactions, with 49 deals totaling over $39 billion since October, as multinational corporations continue to expand in China [6] - The upcoming JPM conference in January 2026 is expected to catalyze further activity in the sector, coinciding with the annual report cycle, suggesting a peak in data disclosures and BD transactions [6]

Group 1 - The core viewpoint of the news is that the innovative drug sector is experiencing a strong surge, with several companies seeing significant stock price increases due to supportive regulatory measures from the National Medical Products Administration (NMPA) aimed at promoting innovative drug development [1] - The NMPA plans to implement precise policies by 2026, focusing on the establishment of a data protection system for drug trials and a market exclusivity system for pediatric and rare disease medications [1] - As of 2026, several new drugs have already been approved, including products from companies like Hengrui Medicine and Zai Lab, with expectations that around 20 major new drugs will receive approval in 2026, covering various therapeutic areas [1] Group 2 - According to Guojin Securities, since 2025, the heat of AI pharmaceutical technology has been rising, and the global innovative drug market remains robust, leading to increased attention in the domestic biopharmaceutical investment sector [2] - The investment strategy for the CXO industry in 2026 focuses on two main lines: prioritizing leading companies with technological advantages and high overseas business ratios to mitigate domestic market uncertainties [2] - The recovery in domestic biopharmaceutical investment is expected to benefit various CRO segments, indicating potential long-term investment value [2]

Core Viewpoint - Rongchang Biopharma announced a significant business development (BD) deal with AbbVie for the RC148 drug, with a total transaction value of up to $5.6 billion, marking a new high for the company in terms of upfront payments and potential total deal value [1][3][8] Group 1: Business Development Deal - The agreement with AbbVie includes an upfront payment of $650 million and potential milestone payments of up to $4.95 billion, along with tiered royalties on net sales outside Greater China [2][5][9] - This deal represents a shift in Rongchang Biopharma's BD strategy, moving from early reliance on multinational pharmaceutical companies to a more flexible collaboration model [1][4][6] Group 2: RC148 Drug Development - RC148 is a novel bispecific antibody targeting PD-1/VEGF, currently undergoing clinical trials for various advanced malignancies [4][9] - The drug has received FDA IND approval for a Phase II clinical trial in the U.S., indicating its entry into global clinical development [4][9] - Preliminary clinical data presented at the ESMO-IO conference showed promising efficacy for RC148 in treating non-small cell lung cancer [4][9] Group 3: Financial Performance - For the first three quarters of 2025, Rongchang Biopharma reported revenues of 1.72 billion yuan, a year-on-year increase of 42.27%, while net losses decreased significantly to 551 million yuan from 1.071 billion yuan in the same period last year [5][10]

Group 1 - Rongchang Biologics announced a collaboration with AbbVie for overseas rights to RC148 (PD1/VEGF dual antibody), receiving an upfront payment of $650 million, up to $4.95 billion in milestone payments, and a double-digit revenue share, indicating strong market potential for PD-1/VEGF dual antibodies [1][3] - The total transaction value for the RC148 licensing agreement is $5.6 billion, which includes the upfront payment and potential milestone payments, exceeding market expectations [3] - The innovative drug ETF, Guotai (517110), rose over 3% following the announcement, reflecting positive market sentiment [1] Group 2 - Kangfang Biologics' partner, Summit Therapeutics, submitted a BLA to the FDA for AK112 (Ivosidenib) to treat EGFR mutation non-small cell lung cancer patients after disease progression on EGFR TKI therapy, with a decision expected by Q4 2026 [3] - Three Life Pharmaceuticals' partner, Pfizer, announced at the 44th J.P. Morgan Healthcare Conference that the PD-1/VEGF dual antibody PF-08634404 (SSGJ-707) will initiate five global Phase III clinical trials for non-small cell lung cancer and other tumor types in 2026 [3] Group 3 - The innovative drug sector is expected to see multiple catalysts entering Q1 2026, with recent developments in small nucleic acids and JPM contributing to positive sentiment in the sector [4] - The domestic CRO (Contract Research Organization) sector is showing signs of recovery, with a significant increase in new orders, indicating a rebound in performance expected in 2026 [4] - The CDMO (Contract Development and Manufacturing Organization) sector continues to show strong demand, with geopolitical risks gradually being resolved [4] Group 4 - Chinese innovative drugs have established significant competitive advantages, including differentiated drug development, high cost-effectiveness, and global compliance capabilities [7][8] - The cost of developing similar targeted drugs in China is approximately one-third of international levels, supported by a large clinical resource base and ongoing "engineer dividend" in the biopharmaceutical sector [7] - Chinese pharmaceutical companies have progressed from "me-too" to "first-in-class" drug development, focusing on unique challenges in hematological and solid tumors, demonstrating the value of differentiated research strategies [7][8]

Group 1 - AbbVie has secured a licensing agreement with Rongchang Biopharma worth up to $5.6 billion, which includes an upfront payment of $650 million and potential milestone payments of up to $4.95 billion [1] - The agreement grants AbbVie exclusive rights to develop, manufacture, and commercialize RC148, a bispecific antibody targeting PD-1 and VEGF, outside of Greater China [1] - RC148 is designed to enhance anti-tumor immune responses while inhibiting tumor-driven angiogenesis, and is currently undergoing clinical trials in China for various advanced malignancies [1] Group 2 - The PD-1/VEGF dual antibody market has seen increased interest, especially after Kangfang Biopharma's dual antibody demonstrated potential superiority over Merck's Keytruda in clinical trials [3] - Major pharmaceutical companies are investing in PD-1/VEGF dual antibodies, with significant licensing deals such as the $6.06 billion agreement between 3SBio and Pfizer, and the $11.1 billion collaboration between Bristol-Myers Squibb and BioNTech [3] - However, following disappointing overall survival data from Kangfang Biopharma's dual antibody, market enthusiasm for PD-1/VEGF dual antibodies has cooled, raising questions about the future potential of this therapeutic class [4] Group 3 - The recent licensing deal between Rongchang Biopharma and AbbVie may indicate a resurgence in interest in the PD-1/VEGF dual antibody space [4] - Kangfang Biopharma's partner, Summit, has submitted a new drug application to the FDA for its PD-1/VEGF dual antibody, targeting specific lung cancer patients, which could further influence market dynamics [4]

北京商报讯（记者 丁宁）1月13日，荣昌生物（688331）高开15.33%，开盘价为110元/股。 消息面上，荣昌生物发布公告称，公司与艾伯维集团控股公司（以下简称"艾伯维"）就RC148签署独家 授权许可协议。艾伯维将获得RC148在大中华区以外地区的开发、生产和商业化的独家权利。协议经相 关监管批准生效后，荣昌生物将收到6.5亿美元的首付款，并有资格获得最高达49.5亿美元的开发、监管 和商业化里程碑付款，以及在大中华区以外地区净销售额的两位数分级特许权使用费。 ...

Core Viewpoint - Rongchang Biologics (09995) experienced a significant stock increase of nearly 9%, closing at 101 HKD, following the announcement of an exclusive licensing agreement with AbbVie for its novel PD-1/VEGF bispecific antibody drug RC148 [1] Group 1: Licensing Agreement Details - On January 12, Rongchang Biologics announced an exclusive licensing agreement with AbbVie for RC148, granting AbbVie exclusive rights for development, production, and commercialization outside Greater China [1] - Rongchang Biologics will receive an upfront payment of 650 million USD and is eligible for up to 4.95 billion USD in milestone payments related to development, regulatory, and commercialization achievements, along with double-digit royalties on net sales outside Greater China [1] - The milestone payments are contingent upon certain conditions, indicating uncertainty regarding the total achievable milestone payment amount [1] Group 2: Product Information - RC148 is a novel bispecific antibody designed to target PD-1 and VEGF pathways, aiming to activate anti-tumor immune responses while inhibiting tumor-driven angiogenesis [1] - The drug is currently undergoing clinical studies in China for treating various advanced malignant solid tumors, both as a monotherapy and in combination therapies [1]