Prof. Annemieke Aartsma-Rus, Leiden University Medical Center, The Netherlands
15:30 - 16:00 Coffee Break
16:00 - 17:10 RNA Therapeutics Development (cont.)
Chair: Prof. Rotem Karni, Israel
REM-422, a small molecule that reprograms RNA processing to target MYB-driven hematological and solid cancers
16:00 - 16:20
Dr. Silvia Buonamici, Remix Therapeutics, Watertown, MA, USA
Oral splicing-regulation therapy for genetic diseases and cancer
16:25 - 16:45
Prof. Masatoshi Hagiwara, MD & PhD, Professor & Chairman, Graduate School of Medicine, Department of Drug Discovery Medicine, Kyoto University, Japan
Neutrophil-specific mRNA delivery - shooting at a moving target
16:50 - 17:10
Prof. Zvika Granot, Faculty of Medicine, Hebrew University, Jerusalem, Israel
Panel Discussion: Transforming Science into Practical Solutions: Insights from the CanceRNA Consortium
17:15 - 18:45
This panel will delve into the critical business and commercialization strategies necessary to translate the CancerRNA Consortium’s research findings into tangible medical solutions and products. We will explore the primary barriers and challenges associated with commercializing RNA-based therapeutics, with a focus on innovations in cancer treatment. Additionally, the discussion will highlight how partners within the CancerRNA Consortium are addressing these challenges to advance effective new anti-cancer therapies.
RNA-based therapeutics – commercialization strategies and challenges Tamar Raz, CEO, Hadasit Medical Research Services and Development, Jerusalem, Israel
Maximizing research impact – Leveraging CANCERNA Scientific Results in Tech Transfer Diana Domínguez, New Ventures Manager, Technology and Business Development Office, Centre for Genomic Regulation (CRG), Barcelona, Spain
IP on RNA Therapeutics Miguel Duarte, Technology Transfer Officer, Institute of Molecular Medicine, University of Lisbon, Portugal
Bridging academia and industry for advanced therapies: RNAble/FutuRx accelerator case study Dr. Amir Mor, RNAble, Ness Ziona, Israel
From bench to product – considerations to advance a molecule into commercial development Simon Geissler, Global CMC Development, Merck Healthcare, Germany
THURSDAY, SEPTEMBER 26, 2024
08:50 - 09:35 RNA Therapeutics Development (cont.)
Chair: Prof. Rotem Karni, Israel
Splice-switching antisense oligonucleotide drug discovery for rare neurodegenerative diseases
08:50 - 09:10
Prof. Michelle L. Hastings, University of Michigan, Ann Arbor, MI, USA
Modulating mRNA stability for genetic diseases and cancer therapy
09:15 - 09:35
Prof. Rotem Karni, The Institute for Medical Research Israel-Canada, Hebrew University-Hadassah Medical School, Israel
09:40 - 10:25 RNA Splicing in Cancer
Chairs: Prof. Juan Valcarcel, Spain; Prof. Michal Lotem, Israel
Opening Remarks
09:40 - 09:45
Prof. Juan Valcarcel, Centre for Genomic Regulation, Barcelona, Spain