
Computation-Driven Innovative Drug R&D Provider
Nucleic acid therapeutics, as the third wave of innovative pharmaceuticals, continue to break through “undruggable” targets, with an explosive growth in pipelines for genetic diseases, metabolic disorders, and oncology. However, challenges such as difficult-to-control off-target effects of siRNA sequences, poor in vivo metabolic stability, and an imperfect preclinical DMPK evaluation system continue to constrain project advancement.
Yadu’s Flagship Creation5-Part Special Series on Nucleic Acid Drugs Live Broadcasts, covering the entire chain from AI-driven design, DMPK, and delivery systems to clinical regulatory submissions and industrialization. It brings together leading pharmaceutical companies and seasoned experts to deconstruct R&D pain points through real-world case studies. Free access for industry professionals!
⏰Live Broadcast Time: June 22, 2026 20:00-21:00
??Lecturer: Gao Xiangrui | Director of the AI Drug Design Platform at XtalPi Technology Innovation Center, Head of Nucleic Acid Drug R&D at XtalPi
Ph.D. in Theoretical Physics from the Chinese Academy of Sciences; former Algorithm Expert at 360, with extensive expertise in the industrial application of AI algorithms. Spearheaded the development of an integrated AI-driven drug design platform for nucleic acids, antibodies, and peptides. Published multiple research outcomes in top-tier international conferences such as AAAI and AACR, accelerating the advancement of multiple siRNA pipelines.
⏰ Live Broadcast Time: June 25, 2026, 20:00-21:00
👨🏫 Lecturer: Dr. Cheng from Hongren Pharma
Ph.D. in Pharmaceutical Analysis from Tongji Medical College, Huazhong University of Science and Technology; Associate Professor and Master’s Supervisor at a university; Part-time Supervisor at multiple pharmaceutical colleges and universities; Young Committee Member of the Chinese Pharmacological Society and the Professional Committee of the Chinese Pharmaceutical Association; Visiting Scholar at Kanazawa University, Japan. Possesses 17 years of experience in bioanalysis and drug metabolism and pharmacokinetics (DMPK) research; has presided over six national-level fund projects; published more than 20 academic papers, including 13 SCI papers as first author or corresponding author; specializes in establishing preclinical in vivo evaluation systems for nucleic acid therapeutics.
✅ Front-end Design: AI tools rapidly optimize siRNA sequences to reduce off-target risks and enhance molecular activity
✅ Preclinical Evaluation: Mastering Small Nucleic Acid-Specific DMPK Standards to Avoid Common Failures in Toxicology and Metabolism Studies
✅ End-to-End Knowledge: One-stop coverage of the entire nucleic acid R&D process, including delivery, regulatory submission, and manufacturing
✅ Practical Insights: Real-World Project Cases from Leading Enterprises to Help You Avoid R&D Pitfalls
✅ Expert Interaction: Live Q&A with Senior Experts in the Field of Nucleic Acid Therapeutics
Click the video account link below to reserve your spot and secure access to the two core dedicated sessions: AI Design and DMPK!