BEGIN:VCALENDAR VERSION:2.0 PRODID:-//ChamberMaster//Event Calendar 2.0//EN METHOD:PUBLISH X-PUBLISHED-TTL:P3D REFRESH-INTERVAL:P3D CALSCALE:GREGORIAN BEGIN:VEVENT DTSTART:20190221T223000Z DTEND:20190222T003000Z X-MICROSOFT-CDO-ALLDAYEVENT:FALSE SUMMARY:NCRAF: CRISPR Babies - Scientific Progress or Ethical Nightmare? DESCRIPTION:CRISPR Babies - Scientific Progress or Ethical Nightmare?\n\n\n\nby \n\n Kirsten Messmer\, PhD\, RAC\n\nPrincipal Regulatory Affairs Specialist\n\nPPD\n\n \n\nAdvanced therapies\, and particularly gene therapies have gained increasing popularity over the recent years. Especially gene therapies offer a potential curative treatment that would eliminate the disease by correcting a misfunctioning or missing gene in a single treatment application. In 2018\, the US FDA released six guidance documents that reflect the agencies current thinking based on the experience gained in clinical application.\n\nGene editing is one of the newer technologies that can be used to manipulate genes. However\, the clinical experience to-date is limited and the increased residual risk is warrants additional safeguards and restrictions in clinical research. In November 2018\, a Chinese scientist announced that the first gene edited babies were born. The revelation stirred a firestorm of controversy over the ethical acceptability of gene editing embryos for implantation due to the remaining uncertainty regarding safety and efficacy.\n\n \n\nThe presentation will summarize the development of gene therapy as promising treatment option and look at some of the techniques employed for gene therapies and gene editing. We will then look at the scientific and ethical implications of the birth of the Chinese gene-edited twins\, Nana and Lulu. X-ALT-DESC;FMTTYPE=text/html:
CRISPR Babies - Scientific Progress or Ethical Nightmare?
\n\n
\nby \;
\n \;Kirsten Messmer\, PhD\, RAC
\nPrincipal Regulatory Affairs Specialist
PPD
\n\nAdvanced therapies\, and particularly gene therapies have gained increasing popularity over the recent years. Especially gene therapies offer a potential curative treatment that would eliminate the disease by correcting a misfunctioning or missing gene in a single treatment application. In 2018\, the US FDA released six guidance documents that reflect the agencies current thinking based on the experience gained in clinical application.
\n\nGene editing is one of the newer technologies that can be used to manipulate genes. However\, the clinical experience to-date is limited and the increased residual risk is warrants additional safeguards and restrictions in clinical research. In November 2018\, a Chinese scientist announced that the first gene edited babies were born. The revelation stirred a firestorm of controversy over the ethical acceptability of gene editing embryos for implantation due to the remaining uncertainty regarding safety and efficacy.
\n\n \;
\n\nThe presentation will summarize the development of gene therapy as promising treatment option and look at some of the techniques employed for gene therapies and gene editing. We will then look at the scientific and ethical implications of the birth of the Chinese gene-edited twins\, Nana and Lulu.
\n