CONFERENCE DAY TWO

MAY 20, 2025

7.30- 8.30: One-on-One Partnering portal meeting schedule starts, to sit down with key contacts up to an hour before day two starts.

8.25: Chair’s Opening Remarks

Developing Molecular Glue Degraders for Disease Targets not Druggable by PROTACs

8.30: Identifying Basal Ligase-Substrate Interactions for Molecular Glue Discovery
• Introducing AlphaSeq, enabling large-scale mapping of basal protein-protein interactions between therapeutically relevant substrates and a diverse repertoire of ligases and chaperones, providing a rich starting dataset for molecular glue discovery
• Sharing how machine learning models can integrate aggregate PPI data to predict neosubstrates and can leverage mutation analysis and structural insights to strengthen binding interfaces and uncover new therapeutic opportunities
• Showing how potentially gluable weak basal interactions can be leveraged for small molecule screening, using the AlphaSeq platform or complementary hit identification approaches

Randolph Lopez

Co-founder & Chief Technology Officer - A-Alpha Bio Inc.

8.50: Panel Discussion - Moving from Phenotypic Screening to Target Based Discovery
• Overview of panellist’s platform technologies to identify glues and degraders including scientific or technical hurdles
platforms address
• How can we combat the diversity in compounds when rationally designing novel candidates?
• What features define a protein as ligandable within a target space?
• How can we provide systematic and scalable screening panels; the debate between biochemical, phenotypical or
computational assays

Randolph Lopez

Co-founder & Chief Technology Officer - A-Alpha Bio Inc.

Giovanni Spagnolli

Chief Technology Officer - Sibylla Biotech srl

Brad Heckmann

Chief Scientific Officer - ASHA therapeutics

Arnout Schepers

CEO - TenAces Biosciences

9.20: Morning Break & Networking

9.30 - 11.00: One-to-One Partnering Meeting Opportunity

New Platforms for Protein Stabilization & Homeostasis: Demonstrating a Pharmacological Audit Trail

11.10: Developing Optimized Folding Interfering Degraders Targeting Cyclin D1
• Providing an overview of folding interference as a new modality to induce the degradation of a target protein
• Demonstrating that folding interfering degraders (FIDs) can be optimized to achieve high potency and desirable ADME properties
• Showing in vitro and in vivo characterization of FIDs acting on Cyclin D1

Giovanni Spagnolli

Chief Technology Officer - Sibylla Biotech srl

11.30: Phosphorylation-Inducing Chimeric Small Molecules – Pairing Kinases with Induced Proximity
• Enabling precise phosphorylation, an important post-translational modification that controls protein function, including activation, stabilization, trafficking, inactivation, and degradation
• Leveraging approach for treating cancer, and other critical immune, metabolic, and rare diseases
• Discussing collaborations to date, and future collaborations

Alexandra Joseph

Chief Scientific Officer - Photys Therapeutics

11.50: Expanding the Realm of Proximity to Achieve Biologically Novel Mechanisms
• Creating novel protein-protein interactions to achieve therapeutic goals not achievable by otherwise targeting individual proteins
• Localizing drug to tissue or cell level of specificity
• Addressing difficult-to-drug targets

Bret Williams

Senior Vice President of Research - Magnet Biomedicine

12.10: Lunch Break & Networking

12.30 – 1.30: One-to-One Partnering Meeting Opportunity

Why Are DACs an Attractive Technology for Pharma? Lowering Toxicity & Improving Efficacy with Increased Tissue Specificity

1.40: Targeted Protein Degraders as Next Generation Antibody Payloads

• Introducing Nurix’s expertise in targeted protein degradation and degrader-antibody conjugates
• The advantages of using degraders as antibody payloads                                                                                                                              • Discussing collaborations

Gwenn Hansen

Chief Scientific Officer - Nurix Therapeutics, Inc.

2.00: Precision ADCs: Engineering Novel Degrader Payloads for Improved Efficacy & Therapeutic Index
• Explaining key design attributes required for making TPDs effective as ADC payloads
• Approaching ADC payload optimization with a medicinal chemistry mindset
• Sharing initial proof-of-concept with a next gen anti-PSMAxSMARCA2/4 DAC for prostate cancer

Andrew Combs

Chief Chemistry Officer - Prelude Therapeutics​

2.20: Panel Discussion - Where do DACs Fit in? Discussing the Decision to Think about Degraders as Payloads
• What is it about small molecule degraders that lend themselves to making good payloads?
• Sharing parameters that allow a degrader protein to be distinct from a toxic payload
• What are some good targets for DACs?
• Collaboration potential between antibody engineering and protein degradation companies

Yue Xiong

Chief Scientific Officer - Cullgen Inc.

Andrew Combs

Chief Chemistry Officer - Prelude Therapeutics​

Gwenn Hansen

Chief Scientific Officer - Nurix Therapeutics, Inc.

2.50: Chair’s Closing Remarks

3.00: Conference Ends