Genedrive PLC Excellent performance data for Genedrive(R) HCV test
April 23 2021 - 2:00AM
RNS Non-Regulatory
TIDMGDR
Genedrive PLC
23 April 2021
REACH
genedrive plc
("genedrive" or the "Company")
Excellent performance of Genedrive(R) HCV -ID Kit in large
multi-centre study
genedrive plc (AIM: GDR), the near patient molecular diagnostics
company, announces the publication of a large independent
multi-centre study evaluating the real-world performance of the
Genedrive(R) HCV -ID Kit in low and middle income countries. The
study yielded sensitivity specifications of 96.2 - 100%, and
specificity specifications of 98.7 - 99.5%, depending on the site
or viral load. The results confirm that the Genedrive(R) HCV -ID
Kit is effective as intended in the diagnosis of HCV infection in
resource limited settings. Importantly, the authors highlight a
test fail rate of only 1.6%, showing that the Genedrive(R) system
performs to this high standard even though the system operators in
the study had no previous experience in molecular testing.
The study, published in the journal Diagnostics (Lamoury et al,
2021, 11, 746) was conducted in Georgia and Cameroon, and enrolled
426 participants, which had very different demographic backgrounds.
The participants in the Georgia trial were almost all intravenous
drug users. Intravenous drug users are a key patient population for
HCV infection. The Genedrive sensitivity and specificity results
were obtained by comparison to testing with the Abbott RealTime HCV
Assay. The publication can be accessed on line at
https://www.mdpi.com/2075-4418/11/5/746 . The study was conducted
by The Foundation for Innovative New Diagnostics (FIND), with grant
funding provided by Unitaid.
The study's findings also corroborate other key performance
capabilities of the Genedrive(R) HCV -ID Kit, including the ability
of the kit to identify all major HCV genotypes, the utility of
requiring small volumes of plasma, and the lack of hazardous
chemicals in the Genedrive kits construction, allowing for normal
disposal processes versus competitor products that require heat
incineration.
David Budd, Chief Executive Officer of genedrive plc, said:
"This study is the first large scale, independent multi centre
evaluation from low and middle income markets using the Genedrive
HCV test. While the performance results are as expected and
excellent, it is equally gratifying to see these achieved with
operators with no previous experience in molecular testing. Moving
testing from highly complex and automated central hospital settings
towards more simple decentralised settings is a balance of
technological complexity, cost, performance, and usability, which
is not always an easy balance to achieve. This study is an
excellent demonstration of real world performance and the ability
of Genedrive to contribute to fighting HCV in resource limited
settings."
The Genedrive(R) HCV -ID Kit allows for decentralised molecular
testing of Hepatitis C (HCV) by PCR, providing results within 90
minutes direct from a small plasma sample (30 ul). This allows for
testing to be done outside of a large hospital facility and indeed
while a patient may be waiting for a result. The assay is performed
on the Genedrive(R) platform, the only truly portable molecular
diagnostics system designed for diagnosing HCV at the point of
need.
For further details please contact:
genedrive plc +44 (0)161 989 0245
David Budd: CEO / Matthew Fowler:
CFO
Peel Hunt LLP (Nominated Adviser
and Joint Broker) +44 (0)20 7418 8900
James Steel / Victoria Erskine
finnCap (Joint Broker) +44 (0)20 7220 0500
Geoff Nash / Kate Bannatyne / Alice
Lane
Walbrook PR Ltd (Media & Investor +44 (0)20 7933 8780 or genedrive@walbrookpr.com
Relations)
+44 (0)7980 541 893 / +44 (0)7876
Paul McManus / Anna Dunphy 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 released a
high throughput SARS-CoV-2 assay and has in development a
Genedrive(R) Point of Care version of the assay, both based on
Genedrive(R) chemistry.
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