CRISPR in Drug Discovery: From Targets to Therapeutics

In accordance with current government guidelines on the COVID-19 pandemic, the third CRISPR in Drug Discovery: From Targets to Therapeutics meeting will be held on 23rd and 24th March 2021 as a virtual event. Genome Engineering, including zinc-finger nucleases, TALENs and most recently CRISPR/Cas9, has become a powerful tool in the drug discovery pipeline. This meeting will focus on the application of genome engineering to identify novel drug targets through large scale CRISPR based functional genomics studies, developing advanced cellular and in vivo disease models for target validation, and the pioneering applications in therapeutic genome editing. A current perspective of the applications of these rapidly developing technologies with a focus on drug discovery applications will be the meeting’s focus. The scientific program for this CRISPR in Drug Discovery meeting will include:

  • Large-scale CRISPR functional genomics studies for drug target identification and validation
  • Application of genome engineering in developing biological models of disease from single cells through to complex in vitro tissue systems and in vivo models
  • Cutting edge CRISPR genome engineering technologies and their emerging applications
  • A perspective from technology leaders toward the future therapeutic applications of genome engineering

We aim to bring together the research community working in the field of genome engineering with interests in developing and applying the technology for pharmaceutical research. Join scientists from academia, pharma, biotech and CRO’s online to hear talks given by speakers at the cutting edge of genome engineering, network at the virtual exhibition and gain strategic insights into solutions for increasing the success of drug discovery and development.

Plenary Keynote Speakers

Dr. Mathew Garnett (Wellcome Sanger Institute)
Dr. Madeline A Lancaster (MRC Laboratory Molecular Biology)
Prof. Jacob Corn (ETH Zurich)

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