Targeted Radiopharmaceuticals Summit EU 2026
8 December 2026 – 10 December 2026
Renaissance London Heathrow Hotel, London, United Kingdom
The 8th Targeted Radiopharmaceuticals Summit Europe, organised by Hanson Wade, brings together scientific, clinical, manufacturing, regulatory and commercial leaders in targeted radiopharmaceuticals and radioligand therapy. The programme runs from a pre-conference seminar day through two main conference days, with parallel tracks on discovery and preclinical development, translational and clinical development, and supply chain and CMC, alongside plenary sessions with regulators, patients and investors.
70 sessions · 50 speakers
Organiser (1)
Media Partner (1)
Sponsors (10)
Trasis · Hiro · Beacon · Chelatec · Isotopia · Almac Group · Comecer · Perceptive · Starget Pharma · Navigo Proteins
Speakers (50)
- Ajaaz Hussain Radiopharmaceutical Scientist, The Royal Marsden NHS
- Rich Edwards Chief Technology Officer, Nuclide Therapeutics
- Chaitanya Divgi Senior Expert - Strategic Therapeutic Innovation, Novartis
- Friedmund Bachmann Vice President CMC & Project Lead, OncoOne
- Graeme McRobbie Associate Director Formulation Science Radiopharmaceuticals, Bicycle Therapeutics plc
- Guangzhou Han Chief Scientific Officer, RadAlliance Therapeutics Inc
- Kevin Tabury Program Pipeline Manager - Head of Innovation & Translational Development Unit, Belgian Nuclear Research Center
- Luke Brzozowski Executive Director, Theranostics, University Health Network
- Martin Steegmaier Chief Scientific Officer, Molecular Partners
- Michael Method Chief Medical Officer, Bicycle Therapeutics
- Mohamad Haqiqian PET Radiopharmacy Production & QC Analyst, Radiation Safety Supervisor, Curium Pharma
- Waisi Eng Chief Technology Officer, Norroy North America Inc.
- Zahra Trippe Patient Engagement Lead Oncology, Bayer
- Vicki Jardine Vice President - Global Clinical Development, Ratio Therapeutics
- Ana Filipa Fonseca Director, Global RLT Strategy and Early Portfolio, Novartis AG
- Andreas Furer Senior Regulatory Manager, Swiss Medic
- Anil Lalwani Director - Regulatory Chemistry, Manufacturing, Controls & MedTech, Telix Pharmaceuticals
- Cara Ferreira Chief Executive Officer, Lumina Pharmaceuticals
- Chris Pak President & Chief Executive Officer, Molecular Targeting Technologies
- David Gauden Chief Executive Officer, Blue Earth Therapeutics Ltd.
- Dirk Pleimes Group Chief Executive Officer & Chief Marketing Officer, PentixaPharm GmbH
- Frederic Desdouits Chief Executive Officer, OranoMed
- Fredrik Frejd Chief Scientific Officer, Affibody AB
- Gary Inwards Sr Pharmaceutical Assessor, MHRA
- Guido Würth Head of Corporate Development & Radiopharma Medical & Health; Sales; Operations, Affibody AB
- Haihong Jin Chief Scientific Officer, Vitsgen Therapeutics, Inc.
- Ilya Folitar Senior Global Program Safety Team Lead and Radiopharmaceutical Safety Lead, Novartis
- Jitka Riedl Associate Principal Scientist, Project Leader, Bicycle Therapeutics
- Josie Gayton Chief Operating Officer, Precirix
- Judson Kimmel Neuroendocrine Cancer & Theranostics Patient / Advocate, Man Up To Cancer
- Julia Publicover Director, Translational Research & Innovation, University Health Network
- Luigi Aloj Professor of Nuclear Medicine, University of Cambridge
- Marc Robillard Chief Scientific Officer & Founder, Tagworks Pharmaceuticals BV
- Mark Dornan Vice President of Pharmaceutical Development and External Manufacturing, Alpha-9 Oncology
- Mark Fielding Director - Chemistry, Manufacturing, Controls, Regulatory Affairs & Radiopharmaceuticals, AstraZeneca
- Ming Xu Vice President - Oncology & Product Team Lead, Bayer
- Muhammet Tanc CEO, Nuclide Therapeutics
- Oystein Soug Chief Executive Officer, Oncoinvent AS
- Richard Pearson CEO, StandardX
- Sandra Hennig Senior RA CMC Strategist, Bayer
- Shefali Kakar Vice President, Global Head PK Sciences - Oncology, Novartis AG
- Sigal Kalmanson Cusnir Chief Executive Officer, Starget Pharma
- Tanja Aarvak Director, Program Management, Alpha Radioligand Therapy, ARTBIO
- Tomohiko Yamane Director - Molecular Imaging Research, Kobe City Medical Center General Hospital
- Dangshe Ma Sr. Dir, Regeneron
- Daniel Squair S&E Manager, Jarlen Capital
- Ian Poburenny Director, Rothschild & Co.
- Kemp Dolliver Director of Research, Brookline Capital Markets
- Kevin Madagan Partner, McGuireWoods
- Kurt Pike Senior Director - External Innovation, JNJ
Agenda
- The Great Isotope Debate: Which Therapeutic Radionuclide Will Define the Next 5 Years of TRP Development? Seven Isotope Specialists, Seven Perspectives. 1 December 2026
- Engineering the Next Generation of Radiopharmaceutical Platforms: Lessons Learned from First-Generation RLTs 1 December 2026
- The Safety Profile Playbook: Advancing Dosage Optimisation & Safety Assessment Strategies for Therapeutic Radiopharmaceutical Development 1 December 2026
- Mastermind Session: Atlas: Mapping Global Therapeutic Isotope Availability to Accelerate Smarter Trial Placement & TRP Development Strategy 1 December 2026
- Building Strategic Academia-Industry Partnerships Across the Radiopharmaceutical Lifecycle: Lessons from UHN’s Integrated Theranostics Ecosystem 1 December 2026
- Alpha vs Beta: Determining When, Where & Why Different Therapeutic Isotopes Deliver the Greatest Clinical Advantage 1 December 2026
- From FAP to B7-H3: What Determines Whether a Radiopharmaceutical Target Successfully Translates to the Clinic? 1 December 2026
- Roundtable Discussion: Translating Global Development Experience into Clinical Success 1 December 2026
- Roundtable Discussion: Where Should the Field Place Its Next Bet? Prioritising the Next Generation of Radiopharmaceutical Targets 1 December 2026
- Roundtable Discussion: Alpha vs Beta – Is There Ever a Universal Winner? 1 December 2026
- Target Selection Strategy Lab: What Makes a Winning Radiopharmaceutical Target? 1 December 2026
- Automation Strategy Lab: Which Radiopharmaceutical Manufacturing Platform Is Right for Your Programme? 1 December 2026
- Expanding Radiopharmaceutical Clinical Trials into Japan: Opportunities, Challenges & Lessons Learned from Trial Execution 1 December 2026
- Beyond Tumour Uptake: Building the Right In Vivo Models for Radiopharmaceutical Translation 1 December 2026
- Reviewing the Manufacturing Innovations Enabling Commercial-Scale TRPs 1 December 2026
- From Discovery to First-in-Human: Navigating the Critical Preclinical Decisions That Determine Translational Success 1 December 2026
- Follow-Up Mastermind Session: Translational Readiness Challenge 1 December 2026
- Follow-Up Mastermind Session: Standardising Dosimetry & Imaging Across Clinical Trial Sites 1 December 2026
- Follow Up Mastermind Session: Stress-Testing Manufacturing Strategies for Commercial Readiness 1 December 2026
- Radiopharmaceutical CDMO Meet & Match: Connecting Developers with the Manufacturing Partners Powering Next Generation TRPs 1 December 2026
- Dosimetry, Imaging & Radiopharmacy Meet & Match: Connecting Developers with the Partners Enabling Precision TRP Delivery 1 December 2026
- Preclinical CRO Meet & Match: Connecting Developers with the Translational Partners Advancing Next-Generation TRPs 1 December 2026
- I am the Person at the End of Your Pipeline: A Patient Perspective on the Future of Radiopharma 2 December 2026
- Navigating Regulatory CMC Challenges Across Kit-Based & Ready-to-Use Radiopharmaceuticals: An Industry Perspective 2 December 2026
- Regulatory Leaders Fireside Chat: Regulatory Perspectives on the Future of Radiopharmaceutical Development: Where Can Greater International Alignment Enable Faster, More Predictable TRP Development 2 December 2026
- Evolution of International Transport Regulations and their application to Radiopharmaceuticals: Balancing Safety, Compliance & Commercial Reality 2 December 2026
- Designing the Optimal Radiopharmaceutical: Matching Target, Ligand Design, Radionuclide and Disease Biology 2 December 2026
- Advancing Alpha Radioligand Therapies into the Clinic: Lessons Learned from Building a First-in-Human Development Programme 2 December 2026
- The RLT Safety Playbook: Advancing Safety Assessment and Long-Term Risk Management for Therapeutic Radiopharmaceutical Development 2 December 2026
- Scaling Gallium-68 Production in the UK: Building Reliable Diagnostic Supply for the Next Generation of Radiopharmaceutical Development 2 December 2026
- Theranostics in Practice: Building the Foundations for Successful Radiopharmaceutical Development 2 December 2026
- Roundtable Discussion: Is Actinium-225 Ready for Mainstream Clinical Adoption? Balancing Scientific Promise with Development Reality 2 December 2026
- Building Global Radiopharmaceutical Manufacturing Networks: From Process Development to Clinical Supply Readiness 2 December 2026
- Breaking the Preclinical-to-Clinical Bottleneck: Advancing Novel Theranostic Radiopharmaceuticals into First-in-Human Trials 2 December 2026
- Re-Engineering the Therapeutic Window: Can Pre-Targeting Overcome the Fundamental Limitations of Conventional Radiopharmaceuticals? 2 December 2026
- Radiation Safety Considerations for Emerging Therapeutic Radionuclides: From Manufacturing Supply to Patient Administration 2 December 2026
- Defining the Right Dose Without Individualisation: Can Clinical Pharmacology & Dosimetry Deliver More Predictable Radioligand Therapy Outcomes? 2 December 2026
- Selecting the Right Radiopharmaceutical CDMO to De-Risk Development, Scale Manufacturing & Support Long- Term Commercial Success 2 December 2026
- Moving Beyond Fixed Dosing: Using Quantitative Dosimetry to Deliver Truly Personalised TRP Treatment 2 December 2026
- Roundtable Discussion: Beyond Regulatory Requirements: Maximising the Value of Toxicology Studies to De-Risk Preclinical Development 2 December 2026
- Leveraging Advanced PET Imaging & Dosimetry to Accelerate Radiopharmaceutical Clinical Trials 2 December 2026
- Expanding Therapeutic Radionuclide Supply to Prevent the Next Major Bottleneck in Radiopharmaceutical Growth 2 December 2026
- Integrating Radiopharmaceuticals into Standard of Care: Navigating Governance, Funding, Capacity, and Real-World Constraints 2 December 2026
- Building an Isotope Refinery: A New Class of Accelerator for the Theranostic Era 2 December 2026
- The Radioligand Flywheel From Multiparameter Optimization to Clinical Momentum 2 December 2026
- Panel Discussion: Why Are Big Pharma Betting on Targeted Radiopharmaceuticals? 2 December 2026
- Investor Strategy Panel: From Specialist Therapy to Standard of Care: What Must Happen for RLTs to Become a Commercially Scalable Oncology Modality? 2 December 2026
- The Site Perspective: Overcoming Operational Barriers to Deliver Successful Radiopharmaceutical Clinical Trials 3 December 2026
- Demonstrating the Clinical Potential of Pb-212 Alpha Therapy: Key Learnings from Phase II AlphaMedix Development 3 December 2026
- Redefining PRRT: Advancing EBTATE Towards a New Standard of Care for Gastroenteropancreatic Neuroendocrine Tumours 3 December 2026
- Targeting Therapy-Resistant Cancer with Radiotheranostics: Preclinical Insights from ALDH1A1- Directed Development 3 December 2026
- One Patient Strategy Doesn’t Fit All: Adapting Patient Engagement Across Diseases, Development Stages & Healthcare Systems 3 December 2026
- Advancing PSMA Radiopharmaceuticals into the Clinic: Lessons Learned from Navigating the CDE Approval Pathway 3 December 2026
- Elevating Precision Radiodiagnostics Beyond Patient Selection to Transform Clinical Decision-Making 3 December 2026
- Accelerating GMP Tech Transfer: Translating Novel Radiopharmaceutical Platforms from Discovery to First-in- Human 3 December 2026
- Reimagining Antibody-Based Radiopharmaceuticals: Using Click-to-Release Technology to Expand the Therapeutic Window Across Multiple Targets 3 December 2026
- Moving Beyond Cell Surface Receptors: Advancing First-in-Class Tumour Microenvironment Targets into the Clinic 3 December 2026
- Leveraging Early Imaging Data to Build Effective Theranostic Strategies Across Novel Targets 3 December 2026
- Developing Robust Drug Product Strategies to Enable Successful Radiopharmaceutical Development 3 December 2026
- From Promising Clinical Signals to Registrational Success: Prioritizing RLT Opportunities for Late-Stage Development 3 December 2026
- Beyond Peptides: Advancing Radio-DARPin Therapeutics from Platform Innovation to Clinical Proof-of- Concept 3 December 2026
- Advancing Terbium-Based Radiopharmaceuticals Manufacturing to Unlock More Versatile Theranostic & Therapeutic Strategies 3 December 2026
- Engineering the Therapeutic Window in HER2 Radioligand Therapy: First-in-Human Experience with Affibody molecule ABY-271 3 December 2026
- Expanding Radiopharmaceuticals Beyond Established Indications Through Engineered Scaffold Proteins 3 December 2026
- QA/QC Think Lab: Benchmarking Quality Assurance & Quality Control Strategies Across Radiopharmaceutical Development 3 December 2026
- Advancing CAIX-Targeted Radiopharmaceuticals: Developing Next-Generation Precision Diagnostics for Clear Cell Renal Cell Carcinoma 3 December 2026
- Mastermind Session: Advancing rhPSMA from Early Clinical Promise to Registrational Success: Overcoming the Phase I–III Bottleneck 3 December 2026
- From Spot Supply to Strategic Control: What Bicycle’s ²¹²Pb Infrastructure Strategy Signals for the Future of TRP Supply Security 3 December 2026
- From Scientific Promise to Commercial Reality: How Should the Industry Prioritise the Next Generation of Radioligand Therapy Opportunities? 3 December 2026
- Future Directions Panel Discussion: One Final Question: What Must the TRP Community Solve Before We Meet Again? 3 December 2026