Explore the Agenda

7:30 am Check In, Morning Coffee & Light Refreshments

8:20 am Chair’s Opening Remarks

From Global Pharma Powerhouses to Regulatory Harmony – Showcasing the Outlook of Next Generation ADCs & Emerging Areas

8:30 am Precision Delivery of Therapeutics with Antibodies Through Biology, Chemistry & AI

Vice President, Research & Head, R&D Technology & Innovation, Amgen
  • How antibodies enable more precise delivery of therapeutic payloads for oncology and beyond to selected tissues and cell types
  • The biological and chemical challenges that determine whether targeted delivery translates into meaningful therapeutic benefit
  • How AI is accelerating the design and optimization of next-generation antibody-enabled delivery systems

9:00 am Evaluating Phase & Product Appropriate Bioconjugate Development

  • Exploring the differing development approaches of ADCs across the preclinical to commercial spectrum
  • Understanding how the bioconjugate landscape now encompasses a wide variety of modalities with differing mechanisms of action and molecular structures
  • Exploring relevant examples of how the requirements for process and analytical development can vary between different conjugates

9:30 am Fireside Discussion: A Regulatory Perspective on the Complexity of Global Policy & Market Dynamics Towards the Next ADC Approval Beyond TOPO-1

  • What are the current regulatory guidelines and regional differences for ADC clinical and commercial pathways?
  • How as a community can we work with the regulators to reduce impact on development timelines and bring ADCs as standard-of-care therapies?
  • How are the regulators navigating complex ADC formats from dual-payload, bispecific and novel conjugation strategies?

10:00 am Morning Break & Networking

Discovery

Discovery Track

Exploring Novel Antibody Engineering to Enhance ADC Performance

4 Sessions

Preclinical & Translational
Clinical Lessons
Process & Analytical Development
Manufacturing & Supply Chain

12:00 pm Lunch Break & Networking

Discovery

Translating ADC Discovery From In Vitro to In Vivo to Assess Potency & Therapeutic Efficacy of Novel Payloads

3 Sessions

Discovery & Development of Click-To-Release ADCs With Enhanced Therapeutic Potential

Co-Founder & Chief Scientific Officer, Tagworks Pharmaceuticals
  • Using the learnings from our first-in-class clinical-stage click-cleavable ADC, TGW101, targeting TAG72, to inform next-generation designs and further expand the ADC target universe into the non-internalising target space
  • Highlighting how the Click-to-Release linker system delivers a highly differentiated safety and efficacy profile across multiple payload classes
  • Discussing protein design considerations and the functional characterisation of our discovery-phase ADCs
Preclinical & Translational
Clinical Lessons
Process & Analytical Development
Manufacturing & Supply Chain

2:30 pm Afternoon Break & Networking

Showcasing Innovative XDC Design Excellence to Improve Efficacy & Tolerability to Widen the Therapeutic Index

3:30 pm A Scalable Lysine Bioconjugation Platform: Reducing Development Burden as Clinical Demand Scales

Associate Director, AstraZeneca
  • Presenting quality-based driven development
  • Showcasing platform establishment
  • Leveraging multiple programme efficiency

4:00 pm Engineering the Next-Generation Antibody-Oligonucleotide Drug Conjugates & Opportunities for New Disease Indications

  • Moving beyond traditional payloads to oligonucleotide conjugates to deliver siRNA-based medicines to patients faster
  • Leveraging the dual capability to open doors to interventions with reduced off-target effects, providing a pathway for highly precise treatments
  • Utilising AOCs for targeted gene silencing: Overcoming the challenge of escaping from cellular compartments and achieving substantial target gene knockdown in solid tumours

4:30 pm Chair’s Closing Remarks

4:45 pm End of Scientific Programme Day Two