Regeneron forms
consortium to accelerate gene sequencing project
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[January 08, 2018] By
Bill Berkrot
(Reuters) - Regeneron Pharmaceuticals Inc
on Monday announced a collaboration with rival drugmakers that will
speed its effort to collect genetic information on 500,000 people in the
UK Biobank database, a project it believes could help accelerate new
drug discovery and improve approval success rates.
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The data will be made available to health researchers anywhere in
the world following a 6-to-12-month period of exclusive access by
consortium members, Regeneron said.
"This is the first case where there will be large-scale human
sequencing linked to large-scale human medical records that will
also be publicly available," Regeneron President and Chief
Scientific Officer George Yancopoulos said in a telephone interview.
Pfizer Inc, AbbVie Inc, AstraZeneca Plc and Alnylam Pharmaceuticals
Inc each agreed to put $10 million toward the effort, funding that
will make it possible to complete exome sequencing of 500,000
participants by the end of 2019, rather than Regeneron's original
timeline of 2022.
The exome is the small percentage of the human genome containing all
coding genes for proteins, which are used as targets for many
medicines.
"This is great example of the lifesciences industry stepping up and
giving back something that is going to help society while also
accelerating our own efforts to come up with new drug targets and
new medicines," Yancopoulos said.
"Historically, (industry) failure rates have been too high and
that's one of the reasons healthcare costs are so high," he said.
"Genetically validated targets have a much higher success rate."
The data linking human genetic variations to human biology and
disease could also help the U.S. National Institutes of Health and
academic researchers make their own discoveries, Yancopoulos said.
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In addition to new funding, rapidly improving technology will hasten
the project. "We have been more than doubling our sequencing
capacity every year," he said.
The UK Biobank is an exceptional partner for the effort, he said,
because of the enormous amount of medical data it has compiled,
including whole-body imaging and periodic MRI scans of the brain,
chest and abdomen in addition to primary care information.
Yancopoulos acknowledged likely limits to genetic variations and
diversity with all subjects coming from the UK and hopes this will
spur similar large-scale efforts with other populations.
"We are looking for other big projects to do. We think this a great
model."
(Reporting by Bill Berkrot in New York; Editing by Matthew Lewis)
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