8:45 am Chair’s Opening Remarks

9:00 am Workshop: Mitigating Toxicity & Ensuring Safety in Claudin-Targeted Cancer Therapies

  • Tomoko Nakajima Executive Director, Astellas Pharma
  • Salah-Eddin Al-Batran Executive Director Bioanalysis and Pharmacokinetics, The Frankfurt Institute of Clinical Cancer Research

Synopsis

  • This workshop will focus on strategies to mitigate toxicity and enhance safety in Claudin-targeted therapies, addressing common side effects and preclinical profiling. Participants will learn about clinical trial designs and approaches to manage patient safety effectively

Delving into Claudin Biology & Translational Success in Claudin-Targeted Therapies

9:30 am Panel Discussion: Insights into Claudin Biology & its Impact On Cancer Progression

  • Siddhartha Roychoudhury Asset Leader, Immuno Oncology Development, Astellas Pharma
  • Hui Zou Chief Scientific Officer, Phanes Therapeutics
  • XueJun Liu Executive director, Translational Medicine, I-MAB Biopharma Co., Ltd.

Synopsis

  • Understanding the dynamic expression patterns of Claudin 18.2, 6, and 9 in different cancer stages and the implications for therapeutic targeting
  • Outlining the role of claudin proteins in tumor microenvironment interactions and how these interactions influence cancer progression and metastasis
  • Identifying how understanding claudin biology can inform clinical strategies and improve therapeutic outcomes, including the development of targeted delivery systems and combination therapies

10:00 am Translational Development: Bridging Preclinical Findings to Clinical Success in Claudin-Targeted Therapies

  • Jou-Ku Chung Global Head, Clinical Pharmacology, I-MAB Biopharma Co., Ltd.

Synopsis

  • Understanding the importance of developing companion diagnostics for Claudintargeted therapies, including the identification and validation of biomarkers to ensure patient selection
  • Showcasing strategies to address challenges in translational development, such as achieving target specificity, managing toxicity profiles, and optimizing therapeutic windows
  • Analyzing case studies highlighting the successful transition of Claudin-targeted therapies from preclinical stages to clinical trials, with a focus on lessons learned and best practices

10:30 am Showcasing Claudin18.2 T Cell Engager for GC & PDAC Malignancies

  • Miguel Gaspar Senior Director Oncology Research and Development, AstraZeneca

Synopsis

  • Reviewing CLDN18.2 expression as a target for GC and PDAC tumours
  • Strategies for increasing the therapeutic index of T cell engagers and application to CLDN18.2
  • Preclinical data on AZD5863 – a clinical stage CLDN18.2 T cell engager

11:00 am Virtual Networking Session

Synopsis

Return to the Networking Zone to reconnect and break down your takeaways so far with your other attendees. Make sure to check out the questions across the different meeting areas!

11:30 am Coffee Break

Assessing Innovative Therapeutic Approaches & Toxicity Management in Claudin-Targeted Therapies

12:00 pm Next-Generation Cell Therapies Targeting Claudin: Overcoming Challenges & Improving Outcomes

  • Jeffrey Erickson Vice President, Business Development, Triumvira Immunologics Inc

Synopsis

  • Showcasing the latest advancements in next-generation cell therapies targeting claudin, emphasizing novel approaches beyond CAR-T
  • Understanding improvements in toxicity profiles and the durability of therapeutic responses in solid tumors
  • Highlighting early clinical data and preclinical insights to illustrate the effectiveness and potential of these innovative therapies

12:30 pm Potent next-gen ISAC targeting Claudin 18.2

Synopsis

Efficacy in low-antigen-density tumors

Demonstrated superiority to ADCs in preclinical studies

Immunologic memory with epitope spreading provides promise of durable responses and prevents recurrence MTD ≥ 12 mg/kg in NHPs with differentiated toxicology profile from cytotoxic ADCs

Preparing for first-in-human clinical trial

12:45 pm Translational Development: Bridging Preclinical Findings to Clinical Success in Claudin-Targeted Therapies

  • Jou-Ku Chung Global Head, Clinical Pharmacology, I-MAB Biopharma Co., Ltd.

Synopsis

  • Understanding the importance of developing companion diagnostics for Claudintargeted therapies, including the identification and validation of biomarkers to ensure patient selection
  • Showcasing strategies to address challenges in translational development, such as achieving target specificity, managing toxicity profiles, and optimizing therapeutic windows
  • Analyzing case studies highlighting the successful transition of Claudin-targeted therapies from preclinical stages to clinical trials, with a focus on lessons learned and best practices

1:00 pm Chair’s Closing Remarks

1:15 pm End of Conference