Genedrive PLC - Positive final recommendation by NICE
Released
Released
Announcement PDF
RNS Number : 6932U
Genedrive PLC
30 March 2023
genedrive plc
("genedrive" or the "Company")
Genedrive® MT-RNR1 ID Test receives positive final recommendation by NICE
NICE issues final guidance for use in the NHS through Early Value Assessment programme
genedrive plc (AIM:GDR), the point of care molecular diagnostics company, announces that,
further to the Company's announcement on 9 February 2023, the UK's National Institute for
Health and Care Excellence (NICE) has today ratified and finalised its recommendation following a
public consultation process that the Genedrive® MT-RNR1 ID Kit can be used by the NHS. The
review was conducted through NICE's Early Value Assessment (EVA) programme, which was
designed to select and recommend new technologies that will make a real difference to patients
and provide the most value for the NHS.
The positive outcome was based on a number of key conclusions, including that the Genedrive®
MT-RNR1 ID Kit can quickly and accurately identify babies with the MT-RNR1 genetic variant who
may be at risk of hearing loss if given aminoglycoside antibiotics, and that no other test is
available to provide results quickly enough to inform decisions on antibiotic prescribing in
emergency care. These conclusions support, and are a consequence of, the Company's strategy
for the development of rapid molecular diagnostics for emergency care.
David Budd, CEO of genedrive plc, said: "We are appreciative of the thorough review conducted
by the NICE team. The final report issued today entirely reflects the preliminary conclusion published
in February. As we continue with commercial roll out and product adoption, the NICE EVA framework
will give us the opportunity to support specific performance and impact data that NHS users and
commissioners may look for in future guidance. NICE, whose guidance is formally applicable to the
NHS in England and Wales, is an internationally respected health authority and the tools and data
supplied in its review will be relevant to the rest of the United Kingdom and to the other international
markets which we are now accessing."
NICE's recommendation on using the Genedrive® MT-RNR1 test in NHS England and Wales
through its EVA program will support additional data generation requirements whilst the test is
being used routinely within NHS sites. It is anticipated that this data collection process will be
several years in duration. Further guidance on data collection from NICE is expected in the coming
months.
NICE's final EVA report can be accessed here:
https://www.nice.org.uk/guidance/indevelopment/gid-hte10009/documents
For further details please contact:
genedrive plc
David Budd: CEO / Russ Shaw: CFO
+44 (0)161 989 0245
Peel Hunt LLP (Nominated Adviser and
Joint Broker)
James Steel / Oliver Duckworth
+44 (0)20 7418 8900
finnCap (Joint Broker)
Geoff Nash / 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 are currently developing a genetic test for CYP2C19
metaboliser status.
The Genedrive® MT-RNR1 ID Kit, selected as 1 of the 10 EVA pilot projects, is the world's first
commercial point-of-care genetic test for emergency care. It helps to avoid irreversible lifelong
hearing loss in specific infants exposed to aminoglycosides by rapidly detecting the m.1555A>G
gene variant that can cause lifelong deafness, allowing for alternative antibiotics to be prescribed.
Product information can be found at https://www.genedrive.com/assays/rnr1-product.php
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