Genedrive PLC - Verification with Beckman Coulter Life Sciences
Released
Released
Announcement PDF
RNS Number : 0677A
Genedrive PLC
25 September 2020
genedrive plc
("genedrive" or the "Company")
Genedrive® 96 SARS-CoV-2 Kit verified with Beckman Coulter Life Sciences RNA
extraction chemistry
genedrive plc (LSE: GDR), the near patient molecular diagnostics company, announces
that the Company has completed initial testing of Beckman Coulter Life Sciences'
RNAdvance Viral RNA extraction chemistry on respiratory swabs in conjunction with its
COVID-19 PCR test. The sensitivity in using the Genedrive Kit with samples from upper
respiratory swabs is equivalent to the existing Genedrive SARS-CoV-2 Kit specification
claim, indicating the Beckman product is suitable for use in the Genedrive testing
workflow. The Beckman RNAdvance kit has now been added to the Genedrive 96 SARSCoV2 Instruction for Use as a validated extraction protocol for swabs. This is an
important technical milestone in transitioning the Genedrive® 96 SARS-CoV-2 Kit to a
fully automated workflow using Beckman's RNA extraction and Biomek automated
workstation.
The Genedrive Beckman collaboration seeks to fully automate the entire laboratory PCR
testing process for COVID-19 PCR. The two companies are continuing to validate the
Genedrive® 96 SARS-CoV-2 Kit on the Biomek i7 automated workstation with both saliva
and respiratory swab specimens extracted using Beckman Coulter Life Sciences'
RNAdvance viral extraction chemistry. While saliva is potentially a more difficult sample
type compared to upper respiratory swabs, work completed to date has been very
promising and the Company remains confident that it could be validated with clinically
acceptable performance.
David Budd, Chief Executive Officer of genedrive plc, said "We have a collaboration
agreement with Beckman Coulter which includes genedrive validating the analytical
parameters of the combined companies' offerings, and Beckman Coulter establishing the
mechanics and automation of the overall workflow. Once our product performance is
established, we plan to introduce the overall solution in stages, beginning with swab-based
claims and then transitioning to saliva claims thereafter. The FDA places specific prospective
clinical performance requirements on validation of saliva samples, which will take additional
time. Our initial US evaluation site is currently being installed following the completion of
our internal validation studies, after which they will validate the end-to-end solution as
required. We will obtain regulatory approvals prior to a final solution release."
genedrive plc
David Budd: CEO / Matthew Fowler: CFO
+44 (0)161 989 0245
Peel Hunt LLP (Nominated Adviser and
Joint Broker)
James Steel / Oliver Jackson
+44 (0)20 7418 8900
finnCap (Joint Broker)
Geoff Nash / Kate Bannatyne / Alice Lane
+44 (0)20 7220 0500
Walbrook PR Ltd (Media & Investor
Relations)
Paul McManus / Anna Dunphy
+44 (0)20 7933 8780 or
genedrive@walbrookpr.com
+44 (0)7980 541 893 / +44 (0)7876 741 001
About genedrive plc (http://www.genedriveplc.com)
genedrive plc is a molecular diagnostics company developing and commercialising a low
cost, rapid, versatile, simple to use and robust point of need molecular diagnostics
platform for the diagnosis of infectious diseases and for use in patient stratification
(genotyping), pathogen detection and other indications. The Company has assays on
market for the detection of HCV, certain military biological targets, and has tests in
development for tuberculosis (mTB). The Company recently announced the development
of a high throughput SARS-CoV-2 assay and a Genedrive® Point of Care version of the
assay, both based on Genedrive® PCR chemistry.
Disclaimer - BEC Products are for research use and not validated for use in diagnostic
procedures.
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