BMI Seminar // Use of human genome variation to invigorate drug discovery and development

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Event details

Date 29.05.2013
Hour 12:1513:15
Speaker Vincent Mooser
Service de biomédecine
Unil - Université de Lausanne, Switzerland
Location
SV1717A
Category Conferences - Seminars
Abstract
Recent discoveries of an abundance of rare functional variants in the human genome open up new opportunities to invigorate drug discovery and development. More specifically, these “gifts by nature” can be used for drug target identification and validation, shortcutting the need to translate data from animal or cellular models into humans. Moreover, the presence of naturally occurring functional genetic variants makes it possible to contemplate a new generation of more decisive, smaller and faster proof-of-concept studies. Here, investigational drugs are tested early in their development in individuals who have the highest chance to respond to, and benefit from the intervention, i.e. those who carry a genetic variant which functionally mirrors the effect of the intervention. The presentation will illustrate the power of these gene-based (i.e. Mendelian) approaches and describe the unique platform, including a large biobank, which is being constructed locally to collect tangible fruits of the “genomic revolution".

Practical information

  • Informed public
  • Free

Organizer

  • SV-BMI
    Host : Prof. P. Aebischer

Tags

BMI sem

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