Explore the Agenda

7:00 am Check In, Morning Coffee & Light Refreshments

7:55 am Chair’s Opening Remarks

Chief Scientific Officer, Iksuda Therapeutics

Striving for the Next Wave of ADC Innovation: Contextualizing Novel ADC Mechanism & Design Validation to De-Risk Future ADC Development & Deliver Differentiated Patient Benefit

8:00 am Panel Discussion: Contextualizing the Current Status of Novel ADC Design & Development to Ensure Future ADC Success & Differentiated Patient Impact

Head of ADC Discovery, Pfizer
Vice President, Research & Head, Protein Therapeutics, Amgen
Chief Scientific Officer, Iksuda Therapeutics
Chief Scientific Officer, Oncology R&D, Pfizer
Senior Vice President, Discovery, Innovent Biologics
  • Evaluating the landscape of ADC therapies one year on: Is the field pursuing the right amount of innovation to secure the next wave of ADCs beyond Topo1?
  • Delving into payload mechanisms and non-traditional ADC design: What avenues of innovation are showing promise and what needs to be demonstrated?
  • Assessing hurdles and opportunities to achieve differentiated ADC clinical profiles and patient impact in crowded oncology indications
  • Peering into the crystal ball: Debating the future direction of the ADC field and pioneering future possibilities

9:00 am WuXiDARx™ Conjugation Technology & Proprietary Payload-Linker Platform: A Powerful Alliance for Next-Generation Dual Payload ADC Development

Chief Technology Officer, WuXi XDC
  • Advancing next-generation dual-payload ADCs to address traditional challenges like drug resistance and narrow therapeutic windows
  • Leveraging WuXiDARx™ technology for flexible DAR1-6 and WuXiTecan2™ hydrophilic linker, enabling streamlined dual-payload construction without antibody engineering
  • Demonstrating a substantially wider therapeutic index alongside significantly enhanced anti-tumor efficacy in proof-of-concept studies

9:30 am Unveiling the Early Clinical Safety & PK Profile of STRO-004 to Understand How Enhanced Design & Preclinical Characterization Links to Differentiated ADC Clinical Performance

Chief Scientific Officer, Sutro Biopharma
  • Laying out the development and vision of STRO-004 leveraging enhanced antibody engineering and linker-payload design to translate into impactful clinical performance against existing ADC therapies
  • Exploring brand-new Phase I clinical safety and PK data targeting Tissue Factor, contextualized with how well STRO-004 translated from cyno monkey preclinical data, to understand ADC clinical benefit and enhanced therapeutic index
  • Highlighting rationale, development and the power of dual payload ADCs to subvert patient resistance mechanisms to single payload ADCs

10:00 am Morning Break & Structured Networking

Discovery Chemistry

Leveraging Novel Payload Mechanisms & Combinations to Combat Topo1 & MMAE Patient Resistance

Theme 1: Striving for Innovative Payload Mechanisms to Advance Beyond the Topo1 Dogma

Presentation Preview: PROTAC ADCs: Incorporating Historical Learnings to Navigate Novel Payload Development Beyond Blind Potency

Associate Director, Medicinal Chemistry, AstraZeneca
  • Highlighting rationale for developing the first reported degrader payloads versus a known oncology target in light of lack of efficacy from small molecule inhibitors
  • Laying out medicinal chemistry approaches to optimize PROTAC payload properties and exploring variety of conjugation approaches
  • Showcasing potent data generated in preclinical models and highlighting next steps in novel payload development

4 sessions

Discovery Biology
Preclinical
Translational Medicine
Clinical Lessons
Process & Analytical Development
Manufacturing & Supply Chain

1:00 pm Lunch & Networking

Discovery Chemistry

Theme 2: Employing Rationale- Driven Dual Payload Combinations to Circumvent Validated Payload Resistance

Presentation Preview: Harnessing the Promise of Dual Payload ADCs to Combat Resistance to Traditional ADCs

Chief Scientific Officer, Callio Therapeutics
  • Designing multi-mechanism, complementary dual payload ADCs to drive deep and durable responses across a broad range of solid tumors
  • Pioneering the next generation of dual payload ADCs featuring rationally selected payload combinations designed to overcome treatment resistance to single-payload ADCs
  • Contextualizing lead dual payload ADC, CLIO-8221, currently in clinical trials, with a second program expected to enter the clinic in late 2026

4 sessions

Discovery Biology
Preclinical
Translational Medicine
Clinical Lessons
Process & Analytical Development
Manufacturing & Supply Chain

4:00 pm Afternoon Break & Scientific Poster Showcase

Demonstrating the Transformative Impact of ADCs to Reshape the Standard of Oncology Care & Deliver Improved Therapeutic Outcomes for Patients in Early-Line Settings

5:00 pm Evaluating I-SPY2 Clinical Data & Toxicity Monitoring to Assess ADC Progression to Early-Stage Oncology Settings in TNBC & HER2+ Breast Cancer

Associate Professor, Medicine & Director, Breast Oncology, Section of Hematology/ Oncology, University of Chicago
  • Contextualizing I-SPY2 trials evaluating progression of ADCs to neoadjuvant and adjuvant settings in TNBC & HER2+ breast cancer
  • Laying out clinical data generated to investigate early-line ADC progression, including recent clinical performance of Enhertu and Datroway
  • Evaluating concerns with ADC-associated side effects, focusing on ILD monitoring, when considering advancement to neoadjuvant settings

5:30 pm Expansion of ADC R&D & Manufacturing Capabilities in a Payload-Linker CDMO

Vice President, Bioconjugation, Veranova
  • Navigating buildout of ADC clinical manufacturing for diverse, highly potent payloads
  • Exploring implementation of bioconjugation and bioanalytical capabilities within R&D
  • Leveraging process and analytical characterization insights from commercial ADCs

6:00 pm Setting the Scene for Novel Combination Partner Approaches for Vedotin-Based ADCs Including PADCEV

Vice President, Global Development Product Lead, Pfizer
  • Contextualizing the significance of combination approaches within the future of ADC patient impact in early-line oncology therapies
  • Laying out the transformative clinical performance of Padcev-Keyruda combination including event free survival in MIBC
  • Addressing the need and opportunity for novel combinations partners to enhance Padcev clinical impact

6:30 pm Chair’s Closing Remarks

Chief Scientific Officer, Iksuda Therapeutics

6:30 pm Evening Drinks Reception

Enjoy an informal end to the busiest conference day. With a backdrop of palm trees and the San Diego sunset, savor a drink of your choice, reconnect with peers, and meet fresh faces to break down your ADC learnings and objectives.

7:30 pm End of Scientific Program Day One