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The ADC Asia Congress 2026 will gather 300+ industry leaders in Singapore to explore the latest innovations in ADC development.

The ADC Asia Congress 2026 emerges as a pivotal gathering in the rapidly evolving Antibody Drug Conjugate industry, where Asia is establishing itself as the epicenter of next-generation ADC development. The congress will unite 40+ industry experts and 300+ attendees from Singapore, China, Japan, South Korea, Australia, and the broader Asia-Pacific region to explore technological innovations, clinical developments, and strategic collaborations in ADC advancement. The event, co-located with several other prestigious biologics conferences, will address critical industry challenges including high development costs and manufacturing complexities, while showcasing breakthrough technologies, real-world applications, and poster presentations highlighting the latest R&D developments. This comprehensive platform reflects the industry's response to increasing global cancer rates and the growing demand for advanced therapeutic options, supported by rising investments and FDA approvals.


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ADC Asia Congress 2026
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Our selected experts will share insights on the latest trends, challenges, and developments in this dynamic field. Engage in unique discussions, learn about cutting-edge scientific discoveries, and explore the future of biopharmaceuticals with these influential thought leaders.


Dr. Paul Song has nearly 30 years of expertise in biotherapeutics drug discovery and development, specializing in immunology and oncology. He is currently the Chief Scientific Officer at GeneQuantum Healthcare in Suzhou, China, where he leads R&D, including new ADC target discovery and the advancement of an innovative bioconjugate pipelines. Dr. Song has been instrumental in establishing GeneQuantum as a global leader in ADCs through cutting-edge technologies.
Previously, he co-founded Curon Bio in Shanghai, China, a biotech venture focused on next-generation immuno-oncology therapeutics, and served as its CSO, laying a strong foundation for the company's rapid growth. He also served as Vice President at Samsung Bioepis in Seoul, Korea, playing a pivotal role in establishing the company as a global leader in biosimilars. Earlier, he was a Principal Research Scientist at Lilly Research Laboratories in Indianapolis, USA. Dr. Song holds a Ph.D. in Biology from Purdue University, USA.


Dr. Heidi Wang is an experienced global drug development and regulatory expert with more than 30 years of Pharmaceutical Industry and Biotech experience. With expertise in oncology, virology, immunology and other therapeutic areas, Heidi led and contributed to shaping strategy and delivering approvals for Bristol Myers Squibb Company (BMS) and now, for OBI and OBIGEN.
Importantly, Heidi’s positive leadership style and inclusive mindset helped to transform company’s culture and processes to optimise their portfolio acceleration and to bring people together. Leveraging her strengths in problem solving, risk mitigation and asking the right questions, coupled with a deep expertise in drug development, Heidi is now guiding OBI, OBIGEN and as a Board member of a Taiwan-based company and her alma mater, Fu-Jen University. She also volunteers as an advisor and mentor to individuals and multiple organisations in the US, Europe and Taiwan.


John Flygare is currently Head of the ADC and Large Molecule Innovation Group at Eli Lilly. John has over 25 years of experience in the biotech and pharmaceutical industry. Most recently, John was Chief Scientific Offiicer of Firefly Biologics, a company he co-founded to focus on Degrader-Antibody Conjugates. Prior to FFB, John held leadership roles at Merck and Genentech. John has also lectured extensively at Stanford University where he has taught >30 undergraduate and graduate courses in organic and medicinal chemistry. John has authored or co-authored >100 publications and is an inventor on >50 issued US Patents


Dr. Chuang received his PhD degree in Medicinal Chemistry from National Tsing Hua University. As a principal investigator in Development Center for Biotechnology (DCB), he led several drug discovery projects especially on oncology field. These topics include Top1 inhibitor, Nek2/Hec1 inhibitor, antibody-drug conjugates (ADC) and proteolysis targeting chimera (PROTAC). After more than 15 years, he left DCB and joined OBI Pharma as the director of Medicinal Chemistry and focusing on developing anti-Trop2 ADC. In 2022, Dr. Chuang co-founded HoneyBear Biosciences, and serve as the CEO.


Ben is the Vice President of Antibody-Drug Conjugates at Hummingbird Bioscience. With more than 16 years’ experience in the biopharma sector, Ben leads the strategy and development of the Antibody-Drug Conjugates platform and programs at Hummingbird Bioscience. Ben also held strategy and preclinical roles since joining Hummingbird Bioscience in 2020.
Prior to joining Hummingbird Bioscience, Ben advised companies on commercial strategy in APAC at ZS Associates, a healthcare-focused management consulting firm. Ben has accumulated a decade of experience in medicinal chemistry research in a wide range of therapeutic areas including oncology, tropical disease, diabetes, cystic fibrosis, and lysosomal storage diseases at Novartis, the Institute of Cancer Research, and the University of Oxford.
Ben holds a M.Chem. in Chemistry and a D.Phil in Organic Chemistry from the University of Oxford.
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Zou Bin is a seasoned executive and has helmed many leadership positions. He is currently an Adjunct Associate Professor at National University of Singapore. Previously, he served as Managing Director at Trinity Innovation Bioventure Singapore (TIBS) and was the CEO of Shanghai Blueray Biopharma where he successfully led the team to develop several candidates into clinic stage. Prior to his venture, Dr. Zou was a Principal Scientist at Novartis Institute for Tropical Disease where he spearheaded the team to the discovery of Phase II clinical trials drug NITD609. He is the author to more than 25 peer reviewed publications.


David Teng-Yi Huang, Ph.D., is Senior Director of ADC Enabling Technologies at OBI Pharma. With expertise in carbohydrate chemistry and glycoengineering, he leads the development of OBI’s proprietary ADC platforms, including GlycOBI®, ThiOBI®, EndoSymeOBI®, and HYPrOBI™. His research focuses on site-specific conjugation, homogeneous ADCs, and novel linker-payload strategies to enhance stability, therapeutic index, and manufacturability. Dr. Huang has advanced multiple clinical and preclinical ADC programs, including dual-payload and bispecific formats, while contributing to OBI’s intellectual property portfolio and business development partnerships. He earned his Ph.D. in Chemistry from National Tsing Hua University and trained at Academia Sinica in glycoscience.


Dr. Moore joined Zymeworks in July 2022 serving as Chief Scientific Officer and heading early stage RnD efforts focused on the development of next generation ADCs and multispecifics, with multiple new therapeutics entered or on track to enter clinical development. Paul has over 25 years of US-based experience in biologics drug discovery and development in biotechnology research, with his career efforts leading to the discovery and development of a range of FDA-approved and clinical-stage biologics for patients. Before joining Zymeworks, Paul served as Vice President, Cell Biology, and Immunology at MacroGenics, where he worked on the development of numerous clinical stage compounds and scientific collaborations with a range of pharmaceutical partners, including Pfizer, Servier, Gilead, Takeda, Janssen, Roche and Zai Labs. He began his biotech career at Human Genome Sciences (HGS), holding several titles within research culminating in Director of Lead Product Development, where he managed various genomic-based target discovery programs including efforts that led to the discovery, development, approval, and commercialization of Benlysta (belimumab) for the treatment of systemic lupus erythematosus. Dr. Moore received a PhD in molecular genetics from the University of Glasgow, performed post-doctoral work at the Roche Institute of Molecular Biology in Nutley, New Jersey, and also holds a degree in Biotechnology from the University of Strathclyde. He has an extensive research record co-authoring over 80 peer-reviewed manuscripts and is a named co-inventor on over 50 issued US patents.


An experienced and versatile Ph.D. pharmaceutical R&D/Scientific Affairs professional with about 15 years of experience including 8 years as Founder and CEO of Pinotbio, Inc. Experience in drug discovery programs in the areas of oncology – 2 INDs and many on-going pre-clinical programs. Formerly patent examiner in Korea Intellectual Property Office (KIPO) and possesses extensive knowledge about patents and related matters. Has led many scientific evaluations and due diligence of licensing/partnership opportunities in the academic institute and industry in the field of oncology. Extensive knowledge and understanding of drug discovery and preclinical development, especially related to Antibody-Drug Conjugate (ADC) platforms and ADC candidates. Deep understanding of medicinal and process chemistry, especially related with camptothecin payloads and ADC linkers.
Currently, CEO of Pinotbio, Inc. – a South-Korea based biotech company focusing on the discovery and development of novel ADC platforms.
Join the roster of esteemed colleagues to discuss what you or your company are bringing to the biopharmaceutical industry.
Choose a plan that fits your role, company, and industry.
Early Bird Rate : SGD 1,495
(Valid until 2nd October 2025)
Registration Open Rate : SGD 1,695
(Valid until 4th December 2025)
Standard Rate : SGD 1,895
(Valid until 5th Feb 2026)
Final Call Rate : SGD 2,095
(Valid until 11th March 2026)
Applicable to company profiles (headquartered within the APAC region):
Job Profiles: Manufacturing, Bioprocessing, Production, USP, DSP, Operations, Site Heads, Drug Substance and Product Manufacturing, Process Development, Quality, Analytics and other related technical designations
Early Bird Rate : SGD 1,995
(Valid until 2nd October 2025)
Registration Open Rate : SGD 2,195
(Valid until 4th December 2025)
Standard Rate : SGD 2,395
(Valid until 5th Feb 2026)
Final Call Rate : SGD 2,595
(Valid until 11th March 2026)
Applicable to company profiles (headquartered outside of the APAC region):
Job Profiles: Manufacturing, Bioprocessing, Production, USP, DSP, Operations, Site Heads, Drug Substance and Product Manufacturing, Process Development, Quality, Analytics and other related technical designations
Early Bird Rate : SGD 4,295
(Valid until 2nd October 2025)
Registration Open Rate : SGD 4,495
(Valid until 4th December 2025)
Standard Rate : SGD 4,695
(Valid until 5th Feb 2026)
Final Call Rate : SGD 4,895
(Valid until 11th March 2026)
Applicable to company profiles:
Job Profiles: Business Development, Marketing, and Sales
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The conference will provide a comprehensive learning experience covering various aspects of the dynamic biopharmaceutical industry, ensuring attendees gain valuable insights and knowledge.
We are committed to ensuring the safety and well-being of all attendees. We will implement rigorous safety measures in line with local health guidelines and regulations. Specific safety measures will be communicated closer to the event date to ensure they align with the most up-to-date health recommendations. Rest assured, your safety is our priority.
Yes, we have a cancellation and refund policy in place. Please refer to our “Cancellation Policy” on our website for details on how to request a refund if you are unable to attend.
We welcome presentation submissions. If you’re interested in speaking at the event, please visit this page on our website for submission guidelines and deadlines.
Our event is designed to cater to a wide range of professionals within the biopharmaceutical industry, including researchers, scientists, executives, regulatory experts, and professionals involved in drug development and manufacturing.
Participants can expect to gain insights from industry experts, network with peers, and stay up-to-date with the latest trends and innovations in biopharmaceuticals
Yes, we have networking sessions, workshops, and social events scheduled throughout the event to facilitate connections and collaborations among attendees.
Yes, we offer sponsorship and exhibition opportunities for businesses and organizations. Please visit our this page on our website for more information.
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