Program: Wednesday, July 22
Please note that this meeting will take place as an in-person event in Boston, Massachusetts and will not live-stream content for virtual participation. The meeting content will be recorded and made available as an on-demand program after the conference.
All presentations are scheduled to be live, in-person presentations at the date and time specified below unless noted otherwise. Program in progress.
*-Short talk from proffered abstract
Wednesday, July 22
- Networking Breakfast
- Fireside Chat
- Plenary Sessions 1-2
- Plenary Session 1: Drug Discovery – Pharma vs Biotech vs Academia
- Plenary Session 2: Technologies, Biomarkers, and Advanced Diagnostics to Guide Target Discovery and Effective Anti-cancer Therapies
- Drugging the Undruggable Sessions 1-3
- Drugging the Undruggable Session 1: Epigenetics
- Drugging the Undruggable Session 2: Transcription Factors
- Drugging the Undruggable Session 3: Synthetic Lethality Beyond DDR
- Challenges in Drug Discovery Sessions 1-3
- Challenges in Drug Discovery Session 1: Biology
- Challenges in Drug Discovery Session 2: Chemistry
- Challenges in Drug Discovery Session 3: Clinical
- Spotlight on Proffered Papers Session
- Poster Session A/Reception
Networking Breakfast
7-8 a.m. | Independence Ballroom West
Fireside Chat
8-8:45 a.m. | Grand Ballroom
Moderator: To be announced
- 8 a.m. | Introduction
- 8:05 a.m. | Fireside Chat
Richard Pazdur
Break
8:45-9 a.m. | Grand Ballroom Prefunction
Plenary Sessions 1-2
9-11 a.m.
Plenary Session 1: Drug Discovery – Pharma vs Biotech vs Academia
Grand Ballroom
Session Chair: William Pao, Revelio Therapeutics, Inc., New York, New York
- 9:05 a.m. | Timothy Heffernan, The University of Texas MD Anderson Cancer Center, Houston, Texas
- 9:35 a.m. | Lilli Petruzzelli, Genentech, Inc., South San Francisco, California
- 10:05 a.m. | James Christensen, Terremoto Biosciences, South San Francisco, California
- 10:35 a.m. | Panel Discussion
Plenary Session 2: Technologies, Biomarkers, and Advanced Diagnostics to Guide Target Discovery and Effective Anti-cancer Therapies
Constitution Ballroom A
Session Chair: Kurt A. Schalper, Yale University, New Haven, Connecticut
- 9:05 a.m. | Advances and impact of circulating molecular biomarkers in oncology drug development
Maximilian Diehn, Stanford University, Stanford, California - 9:30 a.m. | Immunogenomic determinants of response and resistance to immune checkpoint blockade
Kellie N. Smith, Johns Hopkins University School of Medicine, Baltimore, Maryland - 9:55 a.m. | High dimensional spatial molecular studies to support target discovery and de-risk therapeutics in oncology
Kurt A. Schalper - 10:20 a.m. | Interpretable image analysis using advanced computational models to support therapeutic decisions in oncology
Issam El Naqa, Moffitt Cancer Center, Tampa, Florida - 10:45 a.m. | Panel Discussion
Break
11-11:20 a.m. | Grand Ballroom Prefunction
Drugging the Undruggable Sessions 1-3
11:20 am-12:50 p.m.
Drugging the Undruggable Session 1: Epigenetics
Grand Ballroom
Session Chair: Johnathan R. Whetstine, Fox Chase Cancer Center, Philadelphia, Pennsylvania
- 11:25 a.m. | New inhibitors, degraders, and stabilizers of epigenetic targets and new approaches to target undruggable proteins
Jian Jin, Icahn School of Medicine at Mount Sinai, New York, New York - 11:45 a.m. | Epigenetic therapies: A path to controlling extrachromosomal DNA and rearrangements
Johnathan R. Whetstine - 12:05 p.m. | Scott A. Armstong, Dana-Farber Cancer Institute, Boston, Massachusetts
- 12:25 p.m. | Panel Discussion
Drugging the Undruggable Session 2: Transcription Factors
Constitution Ballroom A
Session Chair: Angela N. Koehler, Koch Institute for Integrative Cancer Research at MIT, Cambridge, Massachusetts
- 11:25 a.m. | Proximity pharmacology and transcription factor drug discovery
Michael A. Erb, The Scripps Research Institute, La Jolla, California - 11:45 a.m. | Direct targeting of the intrinsically disordered transactivation domain of androgen receptor enables transcriptome-selective pharmacology
Marianne D. Sadar, BC Cancer Research, Vancouver, British Columbia, Canada - 12:05 p.m. | Kimberly Stegmaier, Dana-Farber Cancer Institute, Boston, Massachusetts
- 12:25 p.m. | Panel Discussion
Drugging the Undruggable Session 3: Synthetic Lethality Beyond DDR
Constitution Ballroom B
Session Chair: Timothy A. Yap, The University of Texas MD Anderson Cancer Center, Houston, Texas
- 11:25 a.m. | Novel synthetic lethal targets
Mathew J. Garnett, Wellcome Sanger Institute, Cambridge, United Kingdom - 11:45 a.m. | Synthetic lethality opportunities for tumors with MMEJ deficiency
Alan D. D’Andrea, Dana-Farber Cancer Institute, Boston, Massachusetts - 12:05 p.m. | Kathryn C. Arbour, Memorial Sloan Kettering Cancer Center, New York, New York
- 12:25 p.m. | Panel Discussion
Lunch on Own
12:50-3 p.m.
Challenges in Drug Discovery Sessions 1-3
3:15-5 p.m.
Challenges in Drug Discovery Session 1: Biology
Grand Ballroom
Session Chair: Paul Workman, The Institute of Cancer Research, London, United Kingdom
- 3:20 p.m. | Integrated bioscience solutions to drug discovery challenges
Paul Workman - 3:50 p.m. | A multi-agent AI system for accurately determining drug mechanism-of-action at scale
Jason M. Sheltzer, Stanford University, Stanford, California - 4:20 p.m. | ELF3-driven epigenetic reprogramming creates ERK pathway dependency in SERD-resistant ER+ breast cancer*
Na Zhang, Dana-Farber Cancer Institute, Boston, Massachusetts - 4:25 p.m. | Dark kinase dependency screening reveals STK17A as a previously unrecognized targetable vulnerability in EGFR-altered glioblastoma*
Eric Spinetti, STARX Therapeutics, Miami, Florida - 4:30 p.m. | Panel Discussion
Challenges in Drug Discovery Session 2: Chemistry
Constitution Ballroom A
Session Chair: Kevan Shokat, University of California, San Francisco, California
- 3:20 p.m. | Kevan Shokat
- 3:50 p.m. | Kyle Seamon, Revolution Medicines, Redwood City, California
- 4:20 p.m. | Targeting the “undruggable” oncogene CCNE1 using a molecular glue degrader in CCNE1 amplified cancers*
Nina Ilic-Widlund, Monte Rosa Therapeutics, Boston, Massachusetts - 4:25 p.m. | enFoldX: AI classification of AlphaFold3-derived structural ensembles enables T cell specificity prediction*
Jonathan Levine, Memorial Sloan Kettering Cancer Center, New York, New York - 4:30 p.m. | Panel Discussion
Challenges in Drug Discovery Session 3: Clinical
Constitution Ballroom B
Session Chair: Puja Sapra, AstraZeneca, Gaithersburg, Maryland
- 3:20 p.m. | Decision making under uncertainty: What actually predicts Ph3 success… and how to improve decision making in the future
Cristian Massacesi, Bristol Myers Squibb, Princeton, New Jersey - 3:50 p.m. | Delivering on precision medicine: Navigating biological purity with operational and commercial realities
Alice T. Shaw, Dana-Farber Cancer Institute, Boston, Massachusetts - 4:20 p.m. | JAB-BX600, a first-in-class EGFR-directed antibody drug conjugate delivering a novel KRAS G12D inhibitor*
Andrea Wang-Gillam, Jacobio (US) Pharmaceuticals, Burlington, Massachusetts - 4:25 p.m. | Patient-level prediction of trial outcomes with a calibrated pan-cancer foundation model*
Samantha Liang, Unlearn.AI, San Francisco, California - 4:30 p.m. | Panel Discussion
Additional Panelist:
Jennifer Euting, Patient Advocate
Break
5-5:15 p.m. | Grand Ballroom Prefunction
Spotlight on Proffered Papers Session
5:15-6 pm | Grand Ballroom
Session Chair: Patricia M. LoRusso, Yale School of Medicine, New Haven, Connecticut
- 5:20 p.m. | Discovery of a next-generation KAT6A inhibitor with an improved therapeutic index and reduced hematotoxicity risk*
Davide D’Alia, Qubit Pharmaceuticals, Paris, France - 5:25 p.m. | VBC106: A first-in-class FOLR1/MSLN targeted tri-specific antibody drug conjugate (ADC) in ovarian cancer, endometrial cancer, lung adenocarcinoma and beyond*
Jing Li, VelaVigo (Shanghai) Limited, Shanghai, China - 5:30 p.m. | DLL3 CAR-T and CAR-NK cell combination therapy promotes synergistic antitumor activity in small cell lung cancer*
Alan Bers, Dana-Farber Cancer Institute, Boston, Massachusetts - 5:35 p.m. | Targeted degradation of cyclin T1 constrains transcription elongation and triggers tumour cell apoptosis*
Janice Wenzheng Neng, University of Cambridge, Cambridge, United Kingdom - 5:40 p.m. | A first-in-class Pin1 degrader provides robust PKPD response and efficacy in PDAC models*
Morgan O’Shea, Larkspur Biosciences, Cambridge, Massachusetts - 5:45 p.m. | GLIO-1 is a selective DHODH inhibitor that is effective in IDH-mutant gliomas and KDM6-mutated cancers*
Diana Shi, Harvard Medical School, Boston, Massachusetts - 5:50 p.m. | CDK4/6 bifunctional degraders overcome CDK4/6i resistance in breast cancer and demonstrate antitumor efficacy in additional tumor types*
Maechen Wang, Memorial Sloan Kettering Cancer Center, New York, New York
Poster Session A / exhibit show / Reception
5:15-7:45 p.m. | Back Bay Ballroom
Evening off / Dinner on own
7:45 p.m.