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EP 118: The role of genetics in drug discovery and development with Dr. Matt Nelson

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Manage episode 396148472 series 2631947
Content provided by Sano Genetics. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Sano Genetics or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.
Summary:

0:00 Introduction

5:45 Lessons learned from 15 years at GSK: How has genetics and drug discovery evolved over time?

8:10 Matt’s seminal 2015 paper: Quantifying the impact of human genetic evidence on the probability of success in drug development

11:40 Which types of genetic evidence are the best drivers of success in clinical trials?

13:30 Matt’s 2023 paper ‘Refining the Impact of Genetic Evidence on Clinical Success’

18:15 Comparing the value of scale in patient-reported data and genotype arrays (e.g. 23andMe) to deep clinical phenotypes and exomes (e.g. UKBiobank)

23:00 The next leaps forward in newborn and population screening

23:50 Targeting genetic subtypes in drug development

26:15 The role of polygenic risk scores in drug development and the early proof of concept studies

28:15 Proactive trial design to exclude participants who might experience safety risks

30:20 Gene editing technologies for rare Mendelian diseases and Verve Therapeutics approach to treating familial hypercholesterolemia

33:40 Looking forward: The role of drug development in preventing disease

35:50 Matt’s transition from GSK to Deerfield and GenScience

38:00 How the role of genetics and genomics in healthcare investment has changed over the past 10 years

39:00 Genscience’s vision to use genomic data for drug discovery and decision-making

43:25 Looking forward: Linking genetic data to electronic health records in the US and Europe

47:50 Closing Remarks

  continue reading

167 episodes

Artwork
iconShare
 
Manage episode 396148472 series 2631947
Content provided by Sano Genetics. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Sano Genetics or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.
Summary:

0:00 Introduction

5:45 Lessons learned from 15 years at GSK: How has genetics and drug discovery evolved over time?

8:10 Matt’s seminal 2015 paper: Quantifying the impact of human genetic evidence on the probability of success in drug development

11:40 Which types of genetic evidence are the best drivers of success in clinical trials?

13:30 Matt’s 2023 paper ‘Refining the Impact of Genetic Evidence on Clinical Success’

18:15 Comparing the value of scale in patient-reported data and genotype arrays (e.g. 23andMe) to deep clinical phenotypes and exomes (e.g. UKBiobank)

23:00 The next leaps forward in newborn and population screening

23:50 Targeting genetic subtypes in drug development

26:15 The role of polygenic risk scores in drug development and the early proof of concept studies

28:15 Proactive trial design to exclude participants who might experience safety risks

30:20 Gene editing technologies for rare Mendelian diseases and Verve Therapeutics approach to treating familial hypercholesterolemia

33:40 Looking forward: The role of drug development in preventing disease

35:50 Matt’s transition from GSK to Deerfield and GenScience

38:00 How the role of genetics and genomics in healthcare investment has changed over the past 10 years

39:00 Genscience’s vision to use genomic data for drug discovery and decision-making

43:25 Looking forward: Linking genetic data to electronic health records in the US and Europe

47:50 Closing Remarks

  continue reading

167 episodes

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