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EP 124: How ReCode Therapeutics is pioneering tissue specific delivery of gene therapies for Primary Ciliary Dyskinesia with John Matthews

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Manage episode 403760256 series 2631947
Inhoud geleverd door Sano Genetics. Alle podcastinhoud, inclusief afleveringen, afbeeldingen en podcastbeschrijvingen, wordt rechtstreeks geüpload en geleverd door Sano Genetics of hun podcastplatformpartner. Als u denkt dat iemand uw auteursrechtelijk beschermde werk zonder uw toestemming gebruikt, kunt u het hier beschreven proces https://nl.player.fm/legal volgen.
0:00 Introduction

01:10 How growing up in Malawi planted the seeds for John’s career in medicine and transition to therapeutic development

04:35 Why John focuses on rare diseases and conditions such as asthma

06:01 What has changed over the last decade in terms of treating and understanding asthma and the progress that genetics has enabled

07:31 What drew John to ReCode and the areas and projects the company is working on
09:20 How clinical loss of function in ciliary cells provides insights into the genetic causes of Primary Ciliary Dyskinesia (PCD) and drives development of relevant therapeutics

11:15 New frontiers: Restoring ciliary cells in subsets of cystic fibrosis and PCD caused by loss of genetic function

13:05 ReCode’s delivery platform: How the company is pioneering tissue specific delivery with lipid nanoparticles.
For more reading on the Salford Lung study and the SORT-LNP platform, scroll to the bottom of the episode information.

16:50 Collaboration: How Sano and ReCode are working together to offer genetic testing to PCD patients to better understand the genetic mechanisms underlying the disease (thinkpcd.com), and what is currently know about the genetics of PCD

19:01 Situs inversus: Prevalence and PCD

20:33 What is currently known about PCD penetrance and inheritance patterns

21:25 Challenges and complexities of drug development in common vs. rare diseases

24:37 Key differences in running clinical trials: rare vs. common therapeutic areas

27:15 How rare disease-focused companies are using natural history data to reduce the need for placebos at clinical trial

30:52 The Liver Forum: the movement to pool natural history data across major clinical trials to provide large, high datasets

33:26 How innovative programmes in the UK are aiming to securely and ethically share data at scale

35:35 Looking to the future: How innovation lies in the ability to use genetics and secure data sharing as a guiding principle for rapidly developing and delivering new treatments

37:21 The importance of data sharing to enable preventative measures

37:43 The transformative power of registries and patient-owned data

41:10 Closing remarks

Explore these papers to learn more about the Salford Lung study and ReCode’s SORT-LNP platform:
  continue reading

176 afleveringen

Artwork
iconDelen
 
Manage episode 403760256 series 2631947
Inhoud geleverd door Sano Genetics. Alle podcastinhoud, inclusief afleveringen, afbeeldingen en podcastbeschrijvingen, wordt rechtstreeks geüpload en geleverd door Sano Genetics of hun podcastplatformpartner. Als u denkt dat iemand uw auteursrechtelijk beschermde werk zonder uw toestemming gebruikt, kunt u het hier beschreven proces https://nl.player.fm/legal volgen.
0:00 Introduction

01:10 How growing up in Malawi planted the seeds for John’s career in medicine and transition to therapeutic development

04:35 Why John focuses on rare diseases and conditions such as asthma

06:01 What has changed over the last decade in terms of treating and understanding asthma and the progress that genetics has enabled

07:31 What drew John to ReCode and the areas and projects the company is working on
09:20 How clinical loss of function in ciliary cells provides insights into the genetic causes of Primary Ciliary Dyskinesia (PCD) and drives development of relevant therapeutics

11:15 New frontiers: Restoring ciliary cells in subsets of cystic fibrosis and PCD caused by loss of genetic function

13:05 ReCode’s delivery platform: How the company is pioneering tissue specific delivery with lipid nanoparticles.
For more reading on the Salford Lung study and the SORT-LNP platform, scroll to the bottom of the episode information.

16:50 Collaboration: How Sano and ReCode are working together to offer genetic testing to PCD patients to better understand the genetic mechanisms underlying the disease (thinkpcd.com), and what is currently know about the genetics of PCD

19:01 Situs inversus: Prevalence and PCD

20:33 What is currently known about PCD penetrance and inheritance patterns

21:25 Challenges and complexities of drug development in common vs. rare diseases

24:37 Key differences in running clinical trials: rare vs. common therapeutic areas

27:15 How rare disease-focused companies are using natural history data to reduce the need for placebos at clinical trial

30:52 The Liver Forum: the movement to pool natural history data across major clinical trials to provide large, high datasets

33:26 How innovative programmes in the UK are aiming to securely and ethically share data at scale

35:35 Looking to the future: How innovation lies in the ability to use genetics and secure data sharing as a guiding principle for rapidly developing and delivering new treatments

37:21 The importance of data sharing to enable preventative measures

37:43 The transformative power of registries and patient-owned data

41:10 Closing remarks

Explore these papers to learn more about the Salford Lung study and ReCode’s SORT-LNP platform:
  continue reading

176 afleveringen

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