NewsBite

ASX Health Stocks: Lumos soars 500pc after US FDA approval for aid to detect bacterial respiratory infections

Lumos Diagnostics’ share price is up more than 500 per cent, thanks to its FebriDx test – which has the potential to reduce antibiotic overuse.

Lumos is flying after a US FDA approval. Picture: Getty Images
Lumos is flying after a US FDA approval. Picture: Getty Images
Stockhead

Lumos Diagnostics (ASX:LDX) is up more than 500 per cent on Monday, thanks to a breakthrough for its FebriDx test for respiratory complains – which has the potential to reduce needless antibiotic use.

The US Food and Drug Administration (FDA) has given the company approval to market its rapid, point-of-care test in the US.

It will be used by healthcare professionals in the diagnosis of bacterial acute respiratory infection and differentiation from non-bacterial etiology in patients presenting in urgent care or emergency care settings.


For the latest health news, sign up here for free Stockhead daily newsletters


That information could reduce antibiotic us – a key concern of health professionals globally as it is recognised as a significant factor behind the growing global emergence of antibiotic-resistant bacteria.

LDX said FebriDx was intended to be used in conjunction with clinical signs and symptoms, including other clinical and laboratory findings, to evaluate patients for acute respiratory infection.

Despite acute respiratory infections being predominantly viral in origin, they are the most common diagnosis for which antibiotics are prescribed, with up to 40 per cent of these considered unnecessary.

As a consequence, one of the core elements of the Centers for Disease Control and Prevention (CDC) Outpatient Antibiotic Stewardship program is to improve antibiotic prescribing by clinicians and their use in patients so that antibiotics are only used when needed.

FebriDx is already registered in the UK, Europe, Canada, UAE, Brazil, Turkey, Pakistan, Singapore, Malaysia and Australia.

Emyria buys Pax Centre as psychedelics laws change

Emyria (ASX:EMD) was up 4 per cent in Monday morning trade after announcing it would l buy the Pax Centre for $1.7 million, payable in a combination of shares (76 per cent) and cash (24 per cent).

The Pax Centre is a leading multidisciplinary psychological trauma care service, serving more than 4000 clients using a comprehensive offering of conventional and emerging therapies.

It currently supports 20 clinicians across psychiatry, mental health nursing, clinical psychology, counselling, social work, occupational therapy and chiropractic care, generating more than $2.6 million of annual billings and has established strong relationships with referrers and major health payers.


MORE FROM STOCKHEAD: Ramsay seeks to sell joint Asian venture | Breast cancer win for INOVIQ | Silk Laser backs $180m bid


EMD is developing psychotherapy treatments using MDMA and psilocybin.

Australia has become the first country to allow psychiatrists to prescribe certain psychedelic substances to patients with depression or post-traumatic stress disorder.

The company said that along with the Pax Centre it was already well advanced to deliver psychedelic-assisted therapy, having:

  • Secure supply of patient-ready MDMA
  • A trained team of therapists and clinicians
  • Ethics-approved care protocol for MDMA-assisted therapy
  • Established an advanced patient data registry

EMD and the Pax Centre are developing care models for psilocybin-assisted therapy for treatment-resistant depression as well as additional clinical trial protocols to broaden and expand the knowledge of how these new interventions work for additional indications.

Rhythm establishes UK subsidiary

Cancer diagnostics technology company Rhythm Biosciences (ASX:RHY) has progressed its market entry strategy for ColoSTAT in the UK with the establishment of a 100 per cent fully owned UK Subsidiary.

The ColoSTAT Test-Kit is Rhythm Bioscience’s simple blood test for the detection of colorectal cancer.

RHY said Rhythm Biosciences UK Limited would assist in the importation and distribution channels of ColoSTAT into the UK and other parts of Europe, with Otto Buttula and Paul Smith as directors of the company.

“Having a local presence in the UK will provide the parent company the opportunity to engage directly with local customers and direct involvement with the supply chain requirements of ColoSTAT,” RHY said in an announcement

The company said the UK market, including England, Scotland, Wales, and Northern Ireland has a population of about 10.7 million people in the current addressable colorectal cancer (CRC) screening market aged from 60 to 74.

The UK uses the faecal immunochemical test (FIT) as a screening methodology, with an approximate participation rate of 67 per cent.


Visit Stockhead, where ASX small caps are big deals


Mach 7 gets US contract for veterans’ health

Health imaging company Mach7 Technologies (ASX:M7T) has announced a multimillion contract to participate in the Veterans Health Administration’s (VHA’s) National Teleradiology Program (NTP) in the US.

As part of the contract M7T will provide its VNA and eUnity Enterprise Diagnostic Viewer solutions which will help form the core of the NTP NextGen PACS architecture.

The VHA NTP is Veterans Affairs’ in-house teleradiology service which has been providing 24x7 service to VHA facilities for more than a decade.

M7T said NTP supported 125 sites across all 18 Veterans Integrated Services Networks (VISNs) and was projected to interpret between 1 and 1.5 million studies annually.

M7T said NTP sought a best of breed, next generation PACS designed, deployed and optimised for its teleradiology workflow and reading environment.

The NextGen PACS program involves two major phases, with Phase I seeing M7T’s VNA and eUnity viewer solutions form the core of NTP’s NextGen PACS, with a potential total contract value (TCV) of $11.7 million with a 12-month implementation/professional service fee period then a fee-per-study subscription licence over a three-year term.

The company said Phase II was contingent upon a number of success factors in Phase I and involved expansion into the Veterans Affairs’ hospital network to support up to seven VISNs with migration, integration and software representing additional potential TCV of $47.9 million over a five-year term.

“As a veteran myself, I’m proud that Mach7 has been given the honour to do its part in supporting our veterans,” M7T CEO Mike Lampron said.

“Beyond the incredible privilege to serve this very special part of our community, this opportunity will allow us to expand our footprint into the US public health sector.”

This content first appeared on stockhead.com.au

SUBSCRIBE

Get the latest Stockhead news delivered free to your inbox. Click here

Read related topics:ASX

Original URL: https://www.theaustralian.com.au/business/stockhead/asx-health-stocks-lumos-soars-500pc-after-us-fda-approval-for-aid-to-detect-bacterial-respiratory-infections/news-story/3ef2c2f73c28073ccdd770ded7c413ea