Synthetic Nucleic Acid Therapeutics: Basic Science, Delivery, and Drug Development (V6)
January 1-5, 2028  | Location to be Determined
David R. Corey, Punit P. Seth and Annemieke Aartsma-Rus
* Session Chair † Invited but not yet accepted | Program current as of September 3, 2026 12 AM | For the most up-to-date details, visit https://www.keystonesymposia.org
Saturday, January 1, 2028
4:00–8:00 PM Registration
6:00–8:00 PM Welcome Mixer
Sunday, January 2, 2028
12:25–5:00 PM On Own for Lunch
7:00–8:00 AM Breakfast
8:00–8:10 AM Welcome Remarks (Joint)
8:10–9:00 AM Keynote Address (Joint)
  David R. Liu †, Broad Institute, HHMI, and Harvard University
Advances in Programmable Genome Editing Technologies
 
9:00–11:15 AM Technological Frontiers of Precision Genome Engineering (Joint)
  Prashant Mali †, University of California, San Diego
Genome and Cell Engineering with Circular RNAs
 
  James Dahlman †, Georgia Tech / Emory Medical School
Targeted in vivo Genome Engineering with Designer Nanoparticles
 
  Kristy Wood †, Intellia Therapeutics, Inc.
Development of in vivo CRISPR Medicines
 
  Short Talk(s) Chosen from Abstracts
 
9:30–9:50 AM Coffee Break
11:15–1:00 PM Poster Setup
11:25–12:25 PM Meet-the-Editor
1:00–10:00 PM Poster Viewing
2:30–4:30 PM Symposia Spotlight 1
  Short Talks Chosen from Abstracts
 
4:30–5:00 PM Coffee Available
5:00–7:00 PM Delivery of Nucleic Acids
  Daniel J. Siegwart †, University of Texas Southwestern Medical Center
Nanoparticle-Mediated Delivery
 
  Julia Alterman †, UMass Chan Medical School
Novel Delivery Designs
 
  Flávia Sousa †, University of Groningen
Biodegradable Polymers
 
  Short Talk(s) Chosen from Abstracts
 
7:00–8:00 PM Social Hour with Dinner
7:30–10:00 PM Posters
Monday, January 3, 2028
7:00–8:00 AM Breakfast
8:00–11:00 AM Clinical Frontiers of Precision Genome Engineering (Joint)
  Benjamin P Kleinstiver †, Massachusetts General Hospital
Development of N=1 Clinical Trials
 
  Amy R. Simon †, Beam Therapeutics
Base Editing Clinical Trial
 
  Bill Lundberg †, CRISPR Therapeutics
Ex vivo/in vivo CRISPR-based Therapeutics
 
  Laura Sepp-Lorenzino †, Intellia Therapeutics
Perspectives on the Future of Genome Editing
 
  Short Talk(s) Chosen from Abstracts
 
9:00–9:20 AM Coffee Break
11:00–1:00 PM Poster Setup
11:00–5:00 PM On Own for Lunch
1:00–10:00 PM Poster Viewing
3:00–4:30 PM Career Roundtable
4:30–5:00 PM Coffee Available
5:00–7:00 PM Rare Disease
  Annemieke Aartsma-Rus, Leiden University Medical Center
ASOs for Rare Disease
 
  David R. Corey, University of Texas Southwestern Medical Center
Gene Activation for Rare Disease
 
  Isabel Aznarez †, Stoke Therapeutics, Inc.
Gene Activation for Rare Disease
 
  Short Talk(s) Chosen from Abstracts
 
7:00–8:00 PM Social Hour with Dinner
7:30–10:00 PM Posters
Tuesday, January 4, 2028
7:00–8:00 AM Breakfast
8:00–11:00 AM Preclinical/Clinical 1
  Hien T Zhao †, Ionis Pharmaceuticals, Inc.
Ionis Update
 
  Brenda L. Bass †, University of Utah
RNA Editing
 
  Alejandro Garanto †, Radboud University Medical Center
RNA Editing
 
  Adrian R. Krainer †, Cold Spring Harbor Laboratory
Talk Title to be Announced
 
  Short Talk(s) Chosen from Abstracts
 
9:00–9:20 AM Coffee Break
11:10–12:10 PM Patient/Family Roundtable
12:10–5:00 PM On Own for Lunch
2:30–4:30 PM Symposia Spotlight 2
  Short Talks Chosen from Abstracts
 
4:30–5:00 PM Coffee Available
5:00–6:15 PM Closing Session (Joint)
  Punit P. Seth, Alnylam Pharmaceuticals
Alnylam Update
 
  Gerald Schwank †, University Zurich
Prime Editing for Inherited Metabolic Diseases
 
  Waseem Qasim †, University in London
Genome-Edited T Cell Therapies for Blood Cancer
 
  Short Talk(s) Chosen from Abstracts
 
6:15–7:00 PM Closing Keynote Address (Joint)
  John M. Maraganore †, City Therapeutics
Novel RNAi
 
7:00–7:15 PM Meeting Wrap-Up: Outcomes and Future Directions
7:00–8:00 PM Social Hour with Dinner
8:00–11:00 PM Cash Bar
8:00–11:00 PM Entertainment
Wednesday, January 5, 2028
12:00–11:59 PM Departure