Program
Please note that this meeting will take place as an in-person event in Toronto 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. Please see the registration page for details.
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
MONDAY, DECEMBER 9
- Welcome and Opening Keynote
- Plenary Session 1: Innovations Opening Up the Potential for Safer Therapeutic Agents
TUESDAY, DECEMBER 10
- Plenary Session 2: Developing Efficacious Drugs with Better Combinability
- Keynote 2
- Plenary Session 3: Engineered Nanoscale Drug Delivery Systems / Modern Formulation-Driven Approaches
- Plenary Session 4: Drug Design and Optimization 1: New and Emerging Targets
- Plenary Session 5: Emerging Frontiers in Bivalent Degraders
WEDNESDAY, DECEMBER 11
- Plenary Session 6: Drug Design and Optimization 2: Brain Penetration
- Keynote 3
- Plenary Session 7: Selective Targeting: Gross Tissue-Restricting and Local (Non-Systemic) Administration (Small Molecule)
Registration
2:30-7 p.m. | Convention Level Foyer
WELCOME AND OPENING Keynote
5:15-6 p.m. | Toronto II + III
- Welcome from cochairs
- Introduction of keynote speaker
Chudi O. Ndubaku, Paraza Pharma, Montreal, QC, Canada - Redefining cancer treatment with tumor targeted modalities: Achievements, opportunities and challenges
Puja Sapra, AstraZeneca, Gaithersburg, Maryland
Plenary Session 1: Innovations opening up the potential for safer therapeutic agents
6-8 p.m. | Toronto II + III
Session Chair: Philip Jones, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania
- Leveraging synthetic lethality for the development of novel cancer therapies
Kimberly J. Briggs, Tango Therapeutics, Boston, Massachusetts - Synthetic lethality: Pathways to therapeutic discovery
Daniel J. Durocher, Lunenfeld-Tanenbaum Research Institute, Toronto, Canada - Structure-guided design and optimization of small molecule CD73 inhibitors with excellent drug-like properties: discovery of quemliclustat*
Jenna Jeffrey, Arcus Biosciences Inc. Hayward, California - Overcoming traditional design limitations with AI-based discovery
David Hallett, Recursion, Oxford, United Kingdom
Opening Reception
8-9:30 p.m. | Toronto I
Breakfast
7-8 a.m. | Convention Level Foyer
Plenary Session 2: Developing efficacious drugs with better combinability
8-9:45 a.m. | Toronto II + III
Session Chair: Chudi O. Ndubaku, Paraza Pharma, Montreal, QC, Canada
- Optimizing drug properties during lead optimization, and laboratory studies to support development of drugs for potential clinical combination
Paul Workman, Centre for Cancer Drug Discovery, The Institute of Cancer Research, London, United Kingdom - Helping academic investigators develop small molecules for the clinic: The NCI developmental therapeutics program and stepping-stones*
Sharad Verma, National Cancer Institute, Bethesda, Maryland - Progress, pitfalls and promise: the journey to effective and well tolerated DNA damage response inhibitor combinations in the clinic
Timothy A. Yap, The University of Texas MD Anderson Cancer Center, Houston, Texas - Preclinical Approaches to Discovery and Development of Novel Combination Therapies
Jerome Mettetal, AstraZeneca, Waltham, Massachusetts
Keynote 2
9:45-10:30 a.m. | Toronto II + III
Session Chair: Chudi O. Ndubaku, Paraza Pharma, Montreal, QC, Canada
- Leveraging conformational dynamics for improved selectivity
James Watters, Relay Therapeutics, Cambridge, Massachusetts
Break
10:30-11 a.m. | Convention Level Foyer
Plenary Session 3: Engineered Nanoscale Drug Delivery Systems / Modern Formulation-Driven Approaches
11 a.m.-12:30 p.m. | Toronto II + III
Session Chair: Philip Jones, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania
- An integrative approach to nanomedicine: leveraging new tools to advance drug delivery
Natalie Boehnke, University of Minneapolis, Minneapolis, Minnesota - Bioengineering cell-based therapeutics
Omid Veiseh, Rice University, Houston, Texas - Strategies to close the translational gap for nanoscale drug delivery systems
Joelle Straehla, Seattle Children’s Research Institute and the University of Washington, Seattle, Washington
Lunch on own
12:30-2 p.m.
Plenary Session 4: Drug Design and Optimization – New and emerging targets
2-4 p.m. | Toronto II + III
Session Chair: Philip Jones, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania
- New targets for treatment of lung cancers
Matthew L. Meyerson, Dana-Farber Cancer Institute, Boston, Massachusetts - EP300 loss of function is a pan-cancer sensitizer to BET inhibition*
Tomas Babak, Leapfrog Bio, San Mateo, California - Discovery of the dual A2A/A2B receptor antagonist MK-1088 for the treatment of solid tumors
Duane DeMong, Merck and Co., Boston, Massachusetts - Mechanistic insights for the advancement of PPARG inverse agonists in muscle invasive urothelial cancer
Jacob I. Stuckey, Flare Therapeutics, Atlanta, Georgia - Discovery of etrumadenant, a first-in-class dual A2a and A2b adenosine receptor antagonist for cancer immunotherapy*
Ehesan Sharif, Arcus Biosciences Inc. Hayward, California
Break
4-4:30 p.m. | Convention Level Foyer
Plenary Session 5: Emerging frontiers in bivalent degraders: from screening to data-driven insights
Session organized by the AACR Cancer in Chemistry Research (CICR) Working Group
4:30-6 p.m. | Toronto II + III
Session Chair: Katherine Donovan, Dana-Farber Cancer Institute
- Title to be announced
Mikko Taipale, University of Toronto, Toronto, Canada - New chemistries to target transcription
Michael A. Erb, The Scripps Research Institute, La Jolla, California - Transferrin receptor targeting chimeras (TransTACs) for targeted degradation of membrane and extracellular proteins in cancer
Xin Zhou, Dana-Farber Cancer Institute/Harvard Medical School, Boston Massachusetts
Poster Session /Reception
6-7:30 p.m. | Toronto I
Breakfast
7-8 a.m. | Convention Level Foyer
Plenary Session 6: Drug Design and Optimization #2 – Brain penetration
8-10 a.m. | Toronto II + III
Session Chair: Chudi O. Ndubaku, Paraza Pharma, Montreal, QC, Canada
- Pan-RAF-MEK molecular glue NST-628 is a potent and brain-penetrant inhibitor of the RAS-MAPK pathway
Klaus Peter Hoeflich, Nested Therapeutics, Cambridge, Massachusetts - Optimization and development of brain penetrant PI3K inhibitors for the treatment of glioblastoma
Laurent Salphati, Genentech, San Francisco, California - Brain penetrant allosteric EGFR inhibitors for NSCLC*
David Scott, Dana-Farber Cancer Institute, Boston, Massachusetts - Discovery of brain-penetrant inhibitors for the treatment of BRAF mutant tumors
Dean Kahn, Ambrosia BioSciences, Boulder, Colorado
Break
10-10:20 a.m. | Convention Level Foyer
Keynote 3
10:20-11 a.m. | Toronto II + III
Session Chair: Philip Jones, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania
- Introduction of keynote speaker
Philip Jones, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania - Bridging the “valley of death” with modern clinical drug development
Patricia M. LoRusso, Yale Cancer Center, New Haven, Connecticut
Plenary Session 7: Selective Targeting – Gross Tissue-Restricting and Local (Non-Systemic) Administration (small molecule)
11 a.m.-12:30 p.m. | Toronto II + III
Session Chair: Philip Jones, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania
- Discovery of DYP688, a first-in-class clinical-stage PMEL17-targeted antibody drug conjugate for the treatment of GNAQ/11-mutant uveal melanoma
Joe Wzorek, Novartis Institute for Biomedical Research, Cambridge, Massachusetts - Dual-drug ADC platform for effective and safe cancer treatment
Kyoji Tsuchikama, The University of Texas Health Science Center, Houston, Texas
Closing Remarks and Departure
12 p.m. | Toronto II + III
- Chudi O. Ndubaku, Paraza Pharma, Montreal, QC, Canada