2026 Yangzhou Biomedical Industry Innovation and Development Conference

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Yangzhou, a vibrant city that blends ancient heritage with modern vitality, is accelerating toward new heights of innovation-driven development with its biomedical industry as a key engine. Leveraging its profound cultural heritage and increasingly robust industrial ecosystem, Yangzhou has hosted the Biomedical Industry Innovation and Development Conference for consecutive years, serving as an important bridge connecting cutting-edge technology with regional economy.

 

On April 24, the "2026 Yangzhou Biomedical Industry Innovation and Development Conference" sets sail once again. This conference is hosted by the Yangzhou Municipal People's Government and organized by the Hanjiang District People's Government of Yangzhou, Yangzhou Municipal Science and Technology Bureau, and Yangzhou High-tech Industrial Development Zone, with professional planning by TONACEA. This marks the fifth consecutive time that TONACEA has served as the professional planner for the Yangzhou Biomedical Industry Innovation and Development Conference.

 

Under the theme "Deepening Win-Win Cooperation, Strengthening the Pharmaceutical Industry," the conference will feature four thematic sessions: Frontier Technologies & Innovative Drug/Device Development; Nucleic Acid Drug Industry Innovation & Development; New Opportunities for Antibody Drugs; and GLP-1 Drugs & AI-Driven Transformation. Numerous leaders and innovation pioneers from the pharmaceutical and healthcare industries have been invited to share insights, deeply explore the logic behind industry transformation, seize strategic opportunities brought by breakthroughs in innovative drugs/devices and AI technologies, promote enterprise win-win collaboration, and drive high-quality industry development.

 

 

 

 

 

TONACEA

01

Opening Ceremony

 

 

 

 

 

Zhang Xingang, Secretary of the Hanjiang District Committee of Yangzhou, presided over the opening ceremony.

 

 

 

 

Remarks by Leaders

 

 

 

Zhao Jianguo

Secretary of the Party Leadership Group of the Jiangsu Provincial Association for Science and Technology

 

As a key part of a major economic province, Yangzhou is developing new productive forces tailored to local conditions with an uplifting spirit of "leading the way and setting an example." After years of dedicated cultivation, the Yangzhou Bio-Health Industrial Park has maintained an annual growth rate of over 30% in industrial scale, rapidly establishing itself among the top tier of the national biomedical industry. The Provincial Association for Science and Technology will, as always, fully support Yangzhou's development, actively introducing high-level innovation resources and talent from both national and provincial levels, providing more solid technological and talent support for Yangzhou's high-quality development.

 

 

Chen Heping

Deputy Director of Jiangsu Provincial Medical Products Administration

 

Biomedicine is a key industry in Jiangsu Province, which has received strong attention from the Provincial Party Committee and Government. In 2025, Jiangsu saw 17 innovative drugs approved for market, accounting for 22.37% of the national total. The number of Class III and Class II medical devices also ranked among the top in the country. The Provincial Medical Products Administration has continuously deepened reforms and provided targeted services, supporting the establishment of an evaluation and inspection sub-center in Yangzhou, which has efficiently processed over a thousand applications. Going forward, we will strengthen policy support, decentralize resources, and innovate services to drive high-quality development of the biomedical industry in Yangzhou and across Jiangsu Province.

 

 

 

Zheng Haitao

Mayor of Yangzhou Municipal People's Government

 

The biomedical industry is the core sector of the life and health industry that Yangzhou prioritizes for cultivation. With Yangzhou High-tech Zone Bio-Health Industrial Park as our main base, we are making every effort to build four synergistic sectors: chemical drugs, biopharmaceuticals, medical devices, and professional services. We have cultivated listed companies such as Aidea and Lianhuan, with sustained innovation vitality and steadily improving industrial competitiveness.

 

The "Yangzhou Biomedical Industry Innovation and Development Conference" has been held for multiple consecutive years and has become an important window showcasing the development of our city's biomedical industry. We sincerely hope that all distinguished guests will exchange ideas, gather insights, build consensus through discussions, and deepen cooperation and achieve results through networking and negotiation. We truly welcome everyone to visit Yangzhou, learn more about Yangzhou, invest in Yangzhou, and become the "best partners" in the high-quality development of Yangzhou's biomedical industry.

 

 

 

 

 

签约仪式

 

 

 

 

 

 

 

 

At this conference, 10 key biomedical projects were signed, covering the entire chain of diagnostics, therapeutics, logistics, and high-end manufacturing, marking the acceleration of coordinated innovation in the regional biomedical industry into the implementation stage.

 

Signed Projects:

  • Nuoling Biotechnology and Northern Jiangsu People's Hospital: Joint Construction of Municipal Intensive Care Medicine Laboratory Project

  • Aidea Pharmaceuticals and Municipal CDC: Infectious Disease Pathogen Microbiology Laboratory Project

  • High-tech Zone: Biopharmaceutical CDMO Base Project

  • High-tech Zone: Super Laboratory and Medical Consumables Base Project

  • High-tech Zone: Shizhiyuan Project

  • Jiangdu District: Nationally Produced 64-slice CT R&D and Industrialization Project Based on AI Technology

  • High-tech Zone: Pharmaceutical Precision Logistics Project

  • High-tech Zone: Pet Multi-Valent Vaccine and Reagent Industrialization Project

  • Guangling District: Intravenous Blood Collection Needle and Nutrition Bag Project

  • Gaoyou City: Low-Temperature Autologous Bone Preservation Project

 

 

 

 

 

Riding the Spring Breeze of This Favorable Land, Embracing the Biomedical Engagement

 

 

 

Yin Gen

Deputy Secretary of the Party Leadership Group of Hanjiang District Government
Secretary of the Party Working Committee and Director of the Management Committee of Yangzhou High-tech Zone

 

Yangzhou High-tech Zone was established in 2001, originating from the Hanjiang Industrial Park. In 2015, it was upgraded to a national high-tech zone with the approval of the State Council. Among its key areas, the Yangzhou Bio-Health Industrial Park, construction of which began in 2015, is the only non-chemical industrial park in Jiangsu Province permitted to produce high-value-added active pharmaceutical ingredients (APIs). It focuses on the bio-health industry, with a primary emphasis on innovative drugs, high-end generic drugs, and high-end medical devices.

 

The park has added 1,200 mu (approximately 80 hectares) of industrial land to build the "Yangzhou Biomedical Innovation Port · Industry Empowerment Center." This center will establish GMP manufacturing facilities and shared R&D platforms, providing full-cycle empowerment services and connecting the critical chain from "pilot-scale testing to mid-scale trial to industrialization." This initiative aims to upgrade the park from a "production base" to an "R&D hub," fostering a biomedical innovation cluster in the Yangtze River Delta region.

 

Invitation Letter

 

🔔 Innovation Partners: You have an innovative drug in the pipeline and are seeking an accelerator for clinical trials and industrialization...

 

🔔 Industry Chain Partners: Trailblazers in medical devices, breakthrough players in high-end generic drugs, enablers of bioprocessing...

 

🔔 City Partners: You care not only about industry but also about quality of life — you want your team to put down roots, your family to thrive, and your career and personal life to flourish...

 

 

 

 

 

R&D Achievement Release

 

 

 

 

Fu Heliang

Chairman of Jiangsu Aidea Pharmaceuticals, a Yangzhou-based listed company

 

Aidea Pharmaceuticals focuses on innovative drugs for HIV treatment. The company has launched Ainuowei (Ainuovir) and its combination product Ainuomiti (Ainuomitin), both of which have been included in the national medical insurance catalog.

 

ACC017, a next-generation integrase inhibitor, demonstrates excellent antiviral activity, low systemic exposure, and favorable resistance profiles, with global patents filed. The single-tablet combination ADC118 has received clinical trial approval. ACC085, a long-acting capsid inhibitor administered once every six months, was granted clinical trial approval in April 2026 for pre-exposure prophylaxis (PrEP).

 

The company plans to raise RMB 1.28 billion through a private placement to advance global clinical development. Over the next five years, Aidea aims to launch seven HIV products.

 

 

 

 

 

TONACEA

02

Plenary Session

 

 

 

 

 

 

Keynote Report

 

 

 

Song Shuo

Chief Analyst of the Healthcare Industry Chain, Research Department, CITIC Securities

 

Innovation-Driven + Policy Optimization: Returning to the Long-Term Growth Trajectory

 

 

The pharmaceutical industry is currently entering a development phase characterized by "innovation-driven + policy optimization." The 2026 government work report designated biomedicine as an emerging pillar industry for the first time. Policies such as drug pricing mechanisms, national reimbursement negotiations, and the "anti-involution" initiative in centralized procurement continue to support genuine innovation.

 

Long-term care insurance is expected to become a nationwide trend, with future annual premiums potentially exceeding RMB 100 billion. Commercial health insurance is poised to unlock hundreds of billions of RMB in payments for innovative drugs and devices.

 

Innovative drugs, CXO, medical devices, and AI-powered healthcare are now entering a harvest period for innovation and global expansion.

 

 

 

Ren Feng

Co-CEO and Chief Scientific Officer, Insilico Medicine

 

 

From Technological Breakthrough to Clinical Validation: The Second Half of the AI-Powered Drug Development Race

 

 

 

Insilico Medicine leverages generative AI platforms (PandaOmics, Chemistry42, etc.) to conduct end-to-end drug R&D from target discovery to clinical validation. Its lead pipeline asset, INS018_055 (a TNIK inhibitor), is the world's first anti-idiopathic pulmonary fibrosis (IPF) drug discovered by AI—from novel target identification to molecule generation. It has completed Phase IIA clinical trials in China and is expected to enter Phase III this year.

 

The company has built a proprietary pipeline of approximately 30 assets, with total external collaboration contract value exceeding US$7.5 billion. By 2025, Insilico had achieved over US$205 million in revenue, validating the commercial value and clinical translational capability of AI-powered drug development.

 

 

Wu Yongqian

Chairman, TransThera Sciences (Nanjing)

 

Lineage Plasticity and Tumor Drug Resistance

 

 

Tumor cell lineage plasticity is a key mechanism driving drug resistance. The company's core product, Tinengotinib, inhibits both the FGFR and JAK pathways, reversing lineage plasticity and restoring sensitivity to hormonal therapies. In prostate and breast cancers, Tinengotinib as monotherapy or in combination with novel endocrine therapies has demonstrated significant efficacy in reversing drug resistance.

 

For cholangiocarcinoma (bile duct cancer), Tinengotinib is the world's first and only next-generation FGFR inhibitor currently in registrational clinical trials, effectively overcoming acquired resistance to existing FGFR inhibitors. Its New Drug Application (NDA) in China has been accepted for review.

 

 

Pan Hai

Chairman, Sciwind Biosciences (Hangzhou)

 

Development Journey of Ecnoglutide: The World's First Approved cAMP-Biased GLP-1 Analog

 

 

Ecnoglutide, developed by Sciwind Biosciences, is the world's first approved cAMP-biased GLP-1 receptor agonist. Leveraging a GPCR-biased signaling mechanism, it selectively activates the cAMP pathway while reducing β-arrestin recruitment, thereby decreasing receptor desensitization and internalization. This results in enhanced weight loss and blood glucose reduction efficacy, while minimizing gastrointestinal adverse effects.

 

Phase III clinical data have demonstrated that Ecnoglutide outperforms semaglutide in weight loss efficacy. In 2026, its weight management indication received approval in China, and the company has entered into commercial partnerships, including with Pfizer.

 

 

Zhao Min

Head of R&D Strategy Asia Pacific, Bayer

 

From Science to Collaboration: How Biotechs Can Select Strategic Partners Among MNCs

 

 

For biotechs seeking partnership with MNCs, a five-step approach is recommended: conduct a thorough self-assessment; study MNC strategies and their patent cliffs; screen target partners; build scientific trust through academic conferences and other channels; and ultimately achieve win-win collaboration.

 

MNCs are strategically focusing on areas such as oncology, metabolism, immunology, neuroscience, and CGT. The core of successful collaboration lies in precise alignment with pipeline gaps, supported by robust data. Biotechs should engage early with global decision-making teams, carefully manage IP and rights balance, and leverage professional advisors to maximize global value.

 

 

 

Liu Shihao

Chairman, HanBio Technology

 

Engineering of SIRP-alfa through AI-assisted Structural Design for Enhanced Safety and Efficacy

 

 

HanBio Technology utilizes AI-assisted structural engineering to design a differentiated SIRPα-Fc fusion protein, HCB101. Through molecular modification, this candidate achieves tumor selectivity: it binds with high affinity to CD47 on tumor cells while avoiding binding to normal cells such as red blood cells, thereby enhancing efficacy and ensuring safety.

 

In Phase I monotherapy study, HCB101 was well tolerated at doses up to 36 mg/kg, with partial responses observed in head and neck cancer and non-Hodgkin lymphoma. In combination therapy, the objective response rate (ORR) reached 80% in second-line gastric cancer, with significant tumor reduction.

 

 

 

 

 

Roundtable Dialogue

 

 

 

 

Roundtable Dialogue

Moderator:

  • Huang Xueying – Chairman, Suzhou Sepax Technologies

Participants:

  • Zhang Jiangli – Chairman, Jiangsu New Horizon Health

  • Niu Ben – General Manager, Jiangsu Lianhuan Pharmaceutical

  • Wang Guoping – General Manager, Yangzhou Oruite Pharmaceutical

  • Mo Qiang – General Manager, Jiangsu Kelun Pharmaceutical

Pharmaceutical Enterprise Innovation in Yangzhou

 

 

 

 

Yangzhou's biomedical industry has developed a significant innovation ecosystem supported by strong policy backing. The government provides dedicated "task force" and "concierge-style" services, enabling rapid approvals and outstanding efficiency in enterprise establishment. Large-scale population screening projects not only serve public health but also help companies accumulate high-quality data, supporting the development of national expert consensus and publications in core journals.

 

On the funding front, patient capital and translational funds have effectively alleviated the pressure of the long and capital-intensive R&D cycle for innovative drugs. Talent recruitment has yielded notable results, with more than half of the PhDs recruited by one company having purchased homes and settled in the city, forming stable teams. On the industrial ecosystem front, leading enterprises, universities, and hospital technology transfer centers are increasingly connecting, creating a synergistic force from R&D to application. Differentiated competition and intelligent manufacturing are also being gradually implemented, driving the industry's continuous upgrade from "1 to N."

 

 

 

 

TONACEA

03

Parallel Sessions

 

 

 

 

Session 1
Frontier Technologies & Innovative Drug/Device Development

 

The integration of next-generation information technology and intelligent manufacturing is driving the transformation of traditional industries. Health service models are shifting from "disease-centered" to "health-centered," with intelligent population health management emerging as a new trend. Significant progress has been made in the R&D of targeted conjugated drugs, in situ neural regeneration for brain repair, scar repair, and other innovative therapeutics, offering new hope for difficult-to-treat diseases.

 

On the technology platform front, gene data-driven precision drug R&D, new drug screening models combining organoids and AI, and globalization pathways for life science tools have become key areas of focus. During the roundtable dialogue, participants engaged in in-depth discussions on the opportunities and challenges for drug and device innovation amidst the wave of frontier technology. There was broad consensus that cross-sector collaboration and industrial AI deployment will accelerate industry transformation.

Group Photo of Some Conference Guests

 

 

 

 

Session 2
Nucleic Acid Drug Industry Innovation and Development

Co-Organizer: Tianjin Quanhecheng Technology Co., Ltd.

 

 

The session was hosted by Zhou Jingjing, R&D Head of Quanhecheng.

 

Broad attention was given to novel lipid nanoparticle nucleic acid delivery systems, chimeric nucleic acid drugs for targeted protein degradation, and non-clinical study strategies for antibody nucleic acid conjugates. Significant progress has been made in the clinical translation of siRNA drugs. Breakthroughs in extrahepatic delivery platform technologies are expanding the application space of oligonucleotide drugs in the treatment of chronic diseases.

 

In addition, areas such as LNP-mRNA-mediated in vivo CAR-T technology, key considerations in nucleic acid vaccine development, and lipid nanoparticle targeted delivery systems have also demonstrated strong R&D vitality.

 

The session focused on the next-generation technology landscape for oligonucleotide drugs, emphasizing that delivery, stability, and targeting are the core bottlenecks to industrialization. Multiple speakers noted that efforts must be made across fundamental research, process development, and capital collaboration to build a self-controlled industrial chain system.

 

 

 

Group Photo of Some Conference Guests

 

 

Session 3
New Opportunities for Antibody Drugs

Organizer: Sepax Technologies

 

(Scroll up/down to view more)

▲ Venue Live Photo

 

The "Antibody Drugs: New Opportunities Forum" invited Dr. Kan Ziyi, CEO of Shanghai Auscan Biopharmaceuticals, to serve as the moderator. Dr. Kan has over 20 years of experience in biopharmaceutical development and industrialization. Prior to joining Auscan, Dr. Kan worked at Pfizer's Global Biologics Center, Allergan, and Ionis Pharmaceuticals, serving as Principal Scientist and Head of CMC Quality Analysis, among other roles. He also served as Vice President of Livzon Mabpharm and Chief Technology Officer of Genor Biopharma, where he was responsible for large-molecule biologics development and regulatory filing, as well as CMC activities related to process, manufacturing, and quality for product industrialization.

 

▲ Kan Ziyi, CEO of Shanghai Auscan Biopharmaceuticals

 

 

First Half

Innovation Landscape of Antibody Drugs in China

 

 

Liu Shihao

Chairman, HanBio Technology

Dr. Liu Shihao has over 30 years of experience in corporate operations and regulatory affairs. His team focuses on tumor immunology. The lead product from their proprietary FBDB platform, HCB101, has shown significant tumor shrinkage in Phase I clinical trials. Dr. Liu previously served as a Global Partner at Fosun and as Co-founder and CEO of Henlius, where he led the development of more than 30 programs and successfully launched over 5 monoclonal antibody drugs in China and Europe.

 

Dr. Liu presented the entire journey of trifunctional ligand fusion proteins from discovery to IND filing in immuno-oncology innovation. He began by addressing the limitations of currently available monospecific antibodies, introduced the functional advantages and application prospects of trifunctional ligands, and highlighted both the challenges and unique benefits of developing trifunctional proteins. He concluded by discussing HanBio's current progress in trifunctional protein pharmacodynamics and CMC case studies.

 

 

Wang Kaixuan

Chief Analyst, Pharmaceutical Industry Chain, CITIC Securities

Wang Kaixuan is currently Vice President at CITIC Securities and Head of the Pharmaceutical Industry Chain Group. His coverage includes multiple sub-sectors such as upstream life science services, CXO, APIs, and generic drugs. He has also supported the investment banking team in IPO offerings for several pharmaceutical companies.

Wang Kaixuan shared insights on the AI-powered drug development industry. He began with an industry overview, introducing progress and cutting-edge cases of supply chain collaboration and multi-technology integration accelerating preclinical R&D. He noted that AI-driven drug pipelines are growing steadily, with higher early-stage clinical success rates. Globally, AI is driving a paradigm shift in pharmaceutical development, with the first profitable company emerging in the space. In China, high-quality AI pharma companies are successively listing on Hong Kong's stock exchanges, and leading CROs have begun their AI transformation journeys.

 

 

Wang Zaiqi

Chairman and CEO, InxMed

Dr. Wang Zaiqi has extensive experience in the innovative drug R&D industry. He has served as a resident physician in internal medicine at Memorial Hospital in the U.S., Director of Clinical Research and Experimental Medicine at Schering-Plough, Clinical Research Director at Merck's Translational Medicine Center (Singapore), and Head of Roche Innovation Center Shanghai. In 2018, he founded InxMed, focusing on drug resistance and metastasis in solid tumors, committed to developing personalized therapies with global impact.

Dr. Wang addressed drug resistance and the tumor microenvironment in cancer treatment. He began by examining cure rates and challenges in cancer patient treatment, highlighting resistance as a core challenge. He then explained how the tumor microenvironment compounds treatment difficulties and promotes resistance. He proposed a multi-strategy combination approach that targets both tumor cells and their supporting microenvironment, achieving synergistic killing effects, effectively overcoming resistance, and ultimately delivering more durable and significant clinical benefits to patients.

 

 

Sun Jian

Director of Formulation Development, TOT Biopharma

Mr. Sun Jian has 15 years of experience in the biopharmaceutical field, with a long-term focus on purification, formulation development, process characterization, and commercial manufacturing facility construction for antibodies and antibody-drug conjugates (ADCs). He possesses full-chain technical capability from laboratory R&D, pilot scale-up, to industrial implementation. With outstanding team management skills, he has led process development and technology transfer for multiple blockbuster biologics, efficiently delivered CDMO projects, and continuously empowered innovative drug R&D and industrialization.

 

Mr. Sun shared insights on the R&D, manufacturing, and development trends of ADCs. He began by analyzing the global ADC market dynamics and evolving landscape, then focused on key CMC challenges throughout the entire process from target discovery to market. Finally, leveraging TOT Biopharma's partnership-driven model, he demonstrated how to support client ADC project success. The presentation progressed systematically from macro industry trends to technical pain points and finally to their own solutions, offering valuable takeaways.

 

 

Second Half

Globalization Opportunities for Biosimilars

 

 

Li Yang

Vice President of CMC Development, CBP (a subsidiary of Innovent Biologics)

Mr. Li Yang has over 10 years of industry experience in biopharmaceutical and vaccine product process, manufacturing, and regulatory filings. He has participated in the launch of five large-molecule products and led or completed process development and IND filings for more than 30 projects across regions including China, the United States, Europe, South America, and Southeast Asia.

 

Mr. Li Yang provided a detailed account of CBP-Innovent's 20,000-liter scale-up manufacturing. On the upstream side, he discussed the construction of high-expressing cell lines and the dual optimization of culture media and processes, achieving both cost reduction and performance improvement. On the downstream side, he compared the process characteristics of membrane chromatography and column chromatography. He also covered formulation and drug delivery system optimization, noting that optimizing delivery systems for high-concentration formulations improves patient convenience. He concluded by summarizing the upstream and downstream scale-up strategies and commercial outcomes achieved at the 20,000-liter scale.

 

 

He Shehui

Senior Director of the Business Development Center, Sinovac Biotech

Mr. He Shehui has 30 years of experience in biopharmaceutical manufacturing, R&D, regulatory affairs, project management, and business development. Since 2020, he has actively advanced internationalization strategies, securing overseas commercialization rights for multiple biosimilars and complex formulations from Chinese pharmaceutical companies. Seizing the opportunity of Phase III clinical trial waivers for biosimilars in Europe and the U.S., since 2025 he has commissioned leading domestic CDMOs to develop seven biosimilars for filing in Europe and the U.S., actively promoting the internationalization of Chinese pharmaceutical companies and their upstream and downstream supply chains.

Mr. He Shehui shared insights into global biopharmaceutical innovation directions, R&D progress, and market landscapes. He discussed key considerations in biosimilar policy, R&D, and commercialization, as well as models for cross-border expansion, technical collaboration, and upstream-downstream supply chain integration. Drawing on successful cases and recent developments, he provided clear strategies and practical references for R&D portfolio planning, market expansion, and win-win cooperation in the biopharmaceutical field.

 

 

Li Jingrong

CTO, GenFleet Therapeutics

Professor Li Jingrong is a specially invited expert at the Senior Training Academy of the National Medical Products Administration (NMPA), an industry professor at China Pharmaceutical University, a visiting professor at the Xi'an Jiaotong-Liverpool University Huihu Lake School of Pharmacy, and a researcher in the Jiangsu Provincial Natural Science Series. Professor Li has over 20 years of experience in pharmaceuticals, particularly in R&D and commercial manufacturing, including pharmaceutical process development, quality control method development, process scale-up, large-scale manufacturing, and upstream/downstream core technologies. His major achievements include three launched biologics, four launched small-molecule drugs, and five launched diagnostic reagent products.

 

Professor Li discussed key aspects of CMC quality control. He began by addressing market and regulatory changes in the industry, elaborating on global market and filing trends. He shared the core of CMC quality control for biosimilars: similarity as the lifeline. He then detailed the critical characterization of biologics, glycan control, and the impact of glycans on drug activity and immunogenicity. Based on glycan considerations, he further elaborated on the risks of innovator drug quality drift for biosimilar quality standards, concluding with key points covering the entire R&D to commercialization process.

 

 

Dou Changlin

CEO & CSO, Anke Biotechnology

Dr. Dou Changlin has held key R&D management positions at the Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Regeneron (U.S.), Genentech (U.S.), A-BIO (Singapore), and Shandong Bo'an Biotechnology. He has over 20 years of experience in the biopharmaceutical field, and multiple of his scientific achievements and patents have been widely applied in the production of several biologics launched globally.

 

Dr. Dou focused his presentation on the waiver of comparative efficacy studies (CES) for biosimilars. He first analyzed the background and significance of regulatory reforms for biosimilars, reviewed international regulatory trends and policy breakthroughs, and interpreted the framework and progress of the ICH M18 guideline. He then elaborated on the scientific basis for waiving CES, analyzed its implementation through international case studies, explored the policy's impact on the biosimilar industry, and ultimately provided recommendations for the development of biosimilars in China, comprehensively presenting the core logic of biosimilar regulatory policy and industry development.

 

 

Session 4
GLP-1 Drugs and AI-Driven Transformation

Organizer: Sepax Technologies

 

(Scroll up/down to view more)

▲ Venue Live Photo

 

Dr. Qin Gang has over 20 years of experience in biologics R&D and management at leading institutions in China and abroad. He has worked at the Max Planck Institute of Biochemistry in Germany and the Chinese Academy of Sciences. He has published numerous original research papers in top-tier international journals and, as a key inventor, has filed over 250 patents both domestically and internationally. Dr. Qin leads a multidisciplinary team that has successfully developed a proprietary, world-leading site-specific enzymatic conjugation technology, as well as the iDiscovery high-throughput intelligent discovery system for XDC drugs and the iConjugation intelligent continuous conjugation manufacturing platform, providing end-to-end solutions for XDC drug development.

 

▲ Qin Gang, Founder & Chairman, Qide Pharmaceuticals

 

 

First Half

GLP-1 Drug Innovation and Commercialization

 

 

Wu Yunfei

Chief Pharmaceutical Analyst, Orient Securities

Dr. Wu Yunfei is deeply engaged in sell-side research in the secondary market of the biopharmaceutical sector. He focuses on research across the entire pharmaceutical industry chain, with emphasis on innovative drug companies, contract research and manufacturing organizations (CXO), and upstream API companies. He has extensive research experience and accumulated achievements in sub-sectors including blood products, IVD, and their upstream supply chains.

 

Dr. Wu focused on the R&D status and trends of GLP-1 drugs, sharing insights from four perspectives: industry transactions, market landscape, domestic deployment, and risks. He pointed out that while the GLP-1 track remains highly active, R&D priorities are quietly shifting. The landscape for multinational pharmaceutical companies is clearly defined, yet gaps remain in oral and ultra-long-acting formulations. He analyzed the current situation of domestic enterprises, noting that while leading companies are well positioned, high-quality targets are relatively scarce. He concluded by highlighting potential industry risks, providing a comprehensive overview of opportunities and challenges in this field.

 

 

Wang Qinghua

Chairman, Yinuo Pharmaceuticals

Professor Wang Qinghua is a nationally appointed expert, a Distinguished Professor at Fudan University, and Deputy Director of the Institute of Endocrinology and Diabetes at Fudan University. He has led major national science and technology innovation projects for new drug development during the 12th and 13th Five-Year Plans. He has received scholarly honors from the Canada Foundation for Innovation (CFI) and the Canadian Diabetes Association (CDA), and serves as a review expert for the CDE drug evaluation center, major national projects, and the National Natural Science Foundation of China (NSFC). His team focuses on translational medicine research in diabetes and metabolic diseases and is responsible for the invention of a series of innovative drugs including Eisupegulutide (Yinuoqing).

 

Professor Wang, drawing on the development journey of Yinuoqing (Eisupegulutide), reviewed the evolution of new drug development in China from generics to original innovation. There is substantial clinical demand for metabolic diseases, and GLP-1 is a scarce, high-quality target. This drug has achieved full-chain independent R&D, with a half-life of up to 204 hours, excellent glucose-lowering and weight-loss efficacy, mild side effects, and the ability to enhance the muscle-to-fat ratio. The product has been successfully commercialized, included in the national medical insurance catalog, and is being deployed both domestically and internationally. The team continues to focus on the metabolic field, with plans to advance multiple original drugs.

 

 

Zhao Chengqing

Director of the Lianyungang Peptide Drug Research Institute, Nuotai Bio

Mr. Zhao Chengqing has 17 years of experience in peptide drug R&D, covering APIs, formulations, pharmaceutical research, clinical project management, and regulatory filings. He has led the completion of clinical trial approvals for over 10 peptide drugs, with 5 varieties approved for market in China (API and formulation). Several peptide APIs have passed regulatory reviews in both China and the U.S. Additional varieties, including tirzepatide, are under development or have been filed. As the lead inventor, he has published and been granted more than ten patents.

 

From a research-to-implementation perspective, Mr. Zhao noted that while the number of peptide drug varieties is small, the individual market value of each variety is extremely high. He deeply analyzed the differences in drug registration classifications and filing pathways for peptide generics in China, the U.S., and Europe. He focused on key pharmaceutical CMC considerations, including starting material selection, process control, and quality control, emphasizing the critical importance of similarity studies, aggregate detection, and impurity control. He also highlighted R&D pitfalls to avoid, providing clear strategies and scientific guidance for global registration of peptide drugs.

 

 

Wu Dongfan

Director, DrugR&D Intelligence

Ms. Wu Dongfan has 12 years of experience across the healthcare industry value chain, including 7 years in medical equity investment and post-investment operations, and over 5 years in BD and alliance management for innovative drugs and cell and gene therapies. She has participated in the management of billion-yuan-level clinical projects, overseen the out-licensing of 4 pipelines and 2 platforms, and been responsible for over 30 R&D collaborations. She previously served as an executive at Fosun Group, focusing on AI-empowered drug R&D.

 

Ms. Wu Dongfan has long focused on AI-empowered drug R&D and is familiar with the collaboration logic and value assessment systems from early discovery to clinical stages. She shared insights and experiences regarding China's first AI-designed GLP-1 small molecule to enter Phase III clinical trials. This small molecule took only four and a half years to reach Phase III, demonstrating significant weight-loss efficacy, a low incidence of side effects, low synthesis costs, and substantial production capacity. It has been granted patents in China, the U.S., and through the PCT system. Leveraging the company's six advanced AI drug discovery platforms, R&D cycles can be significantly shortened, and costs reduced.

 

 

Second Half

The AI + Biologics Innovation Path

 

 

Xu Jinbo

Founder, MoleculeMind

Professor Xu Jinbo is a Fellow of the International Society for Computational Biology (ISCB Fellow) and is widely recognized as a pioneer of AI-driven protein folding. In 2016, he developed the RaptorX-Contact method, which for the first time demonstrated that AI could significantly improve the accuracy of protein structure prediction, inspiring DeepMind to develop AlphaFold. He previously served as a senior researcher at Illumina, and his RAPTOR and RaptorX software are widely used by companies including Merck and Genentech. In 2022, he was the only representative from mainland China invited to participate in the Nobel Foundation Symposium.

 

Professor Xu noted that generative AI is driving biopharmaceuticals into a new era driven by computational design, enabling a paradigm shift from "discovery" to "creation." He introduced MoleculeMind's proprietary multimodal AI protein large model and the MoleculeOS platform, and demonstrated, using multiple experimental data points and case studies, the technological breakthroughs and industrial value of AI-empowered biologics design, outlining the next-generation, computation-driven paradigm for drug development.

 

 

Kang Yun

Founder, Mojing Biotech

Dr. Kang Yun has over 25 years of full-chain experience at leading biopharmaceutical companies including Pfizer, Eli Lilly, Innovent, and GenSci. He has participated in or led the launch of more than 20 products, generating billions of dollars in annual sales. He has led numerous globally pioneering successful cases of AI applications in biopharmaceuticals, covering molecular design, process development, and formulation, significantly shortening timelines and reducing costs, while achieving commercial production line implementation (a world first). He has published 20 papers and holds over 20 patents or patent applications.

 

Dr. Kang's presentation focused on the application of AI in biopharmaceutical CMC and manufacturing, illustrated with real-world examples of commercial production line deployment. He proposed that companies integrate machine learning black-box models with mechanism-based models to create hybrid AI agents, enabling compliant optimization of process parameters. This approach can significantly increase production capacity yields, reduce impurities and production costs, while maintaining product quality. It also enables traceability of production deviations and continuous process iteration, laying the foundation for improving quality and efficiency in pharmaceutical manufacturing and for the development of future smart factories.

 

 

Guo Hongbo

Executive Director, Institute for General Artificial Intelligence Research

Mr. Guo Hongbo has previously worked at Alibaba, Baidu, and Huawei, with extensive experience in large-team management, AI productization, commercial applications, and industrial deployment. In 2025, he led the establishment of the Institute for General Artificial Intelligence Research and serves as its Executive Director. The institute was jointly established by the Changzhou Municipal Government and the Yangtze River Delta National Center for Technology Innovation, focusing on reinforcement learning and decision-making intelligence, combining large model technologies to promote continuous learning applications in digital and physical agents across scientific and industrial directions.

 

Mr. Guo Hongbo shared insights on AI-driven automated scientific experimentation, noting that AI is driving research toward a new paradigm of self-evolution. He reviewed key technological breakthroughs from neural networks to reinforcement learning and AlphaFold, introducing the Memento and AgentFly frameworks, based on memory and reflection mechanisms, which enable large-model agents to engage in continuous self-learning. Using the HEBO Bayesian optimization system, he demonstrated AI-driven automation applications in fields such as materials, drug discovery, and physics experiments, achieving full-process autonomous iteration and significantly improving efficiency, outlining a future research landscape driven by intelligent agents.

 

 

 

 

 

TONACEA

04

"Yangzhou Biopharma Professionals" Networking and Matchmaking Exchange

 

 

 

 

On the eve of the conference, the "High-Level Collaboration: University-Enterprise Two-Way Engagement" Yangzhou Biopharma Professionals Exchange and Jiangsu Education-Industry Dialogue & Matchmaking Event was successfully held at the Hehuachi Campus of Yangzhou University. The event was hosted by Yangzhou University and Yangzhou High-tech Industrial Development Zone, with co-organizers including the School of Chemistry and Materials, the School of Veterinary Medicine, the School of Biological Science and Technology, the Faculty of Medicine of Yangzhou University, and TONACEA.

 

Under the theme "Gathering Wisdom in Yangzhou, Innovating for the Future," the event aimed to showcase the research and talent resources of Yangzhou University in the biopharmaceutical field, build precise bridges for university-enterprise collaboration, and facilitate the translation of scientific and technological achievements into industrial demand-driven applications.

 

 

 

Zhao Wenming, Vice President of Yangzhou University; Zhang Chuanbo, Deputy Director of the Management Committee of Yangzhou High-tech Zone; and Ge Haiyan, Fourth-Level Researcher of Jiangsu Provincial Department of Education, delivered speeches, interpreting industrial policies and the local business environment. The Faculty of Medicine, School of Biological Science and Technology, School of Veterinary Medicine, and School of Chemistry and Materials of Yangzhou University shared academic resources in clinical translation, biopharmaceuticals, veterinary medicine, and chemical pharmaceuticals. During the roundtable dialogue, representatives from enterprises and universities exchanged insights on technical challenges and talent collaboration needs, while industry associations and investment institutions shared trends and directions for capital support, aiming to deepen university-local government and university-enterprise cooperation.

 

 

 

 

 

 

 

TONACEA

05

Conference Highlights

 

 

 

 

 

 

 

 

 

 

 

部分与会嘉宾合影

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

展商风采

 

 

同写意执行团队部分成员

 

 

 

 

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