Viromed Medical AG Seeks Special Approval for Cold Plasma Device for the Prevention of Ventilator-Associated Pneumonia (VAP)
July 10 2024 - 2:48AM
Business Wire
- Targeted use of the antimicrobial effect of cold plasma beyond
wound treatment
- Use of cold plasma could revolutionize the treatment of VAP and
significantly reduce mortality
- Aiming for rapid special approval for own device in Germany and
USA by 2025
Viromed Medical AG (ISIN: DE000A3MQR65; "Viromed") is launching
a second pioneering study on the use of cold plasma for the
prevention of ventilator-associated pneumonia (VAP). The study,
under the scientific direction of Prof. Dr. Hortense Slevogt from
the Hannover Medical School (MHH) and two other world-renowned
institutes, aims to obtain rapid special approval for the PulmoPlas
device developed by Viromed for this innovative preventive measure
in Germany and the USA.
The further development and standardization of cold plasma
technology for use in study-relevant cell cultures and later also
in the human lung comes from relyon plasma GmbH, a wholly owned
subsidiary of TDK Electronics AG. As a partner of Viromed, relyon
plasma will establish the prototypes for the application and ensure
the standardized generation of cold plasma as well as its
characterization and consistency in the trial.
The exploitation rights are held by Viromed Medical AG.
VAP is a frequent and serious complication in mechanically
ventilated patients. It occurs in patients who are invasively
mechanically ventilated for at least 48 hours. Studies show that
VAP occurs in 23 to 36 percent of mechanically ventilated patients
and is associated with prolonged ventilation time and longer stays
in the intensive care unit and hospital. The estimated mortality
rate is 10 to 13 percent. In Germany alone, there were around
486,000 mechanically ventilated intensive care patients in 2023 and
many thousands of deaths, with a strong upward trend. Many millions
of patients worldwide are mechanically ventilated every year. The
use of cold plasma against VAP would therefore have the potential
to save hundreds of thousands of lives every year.
Uwe Perbandt, CEO of Viromed Medical AG: "The use of cold
plasma has already proven very successful in the treatment of
difficult-to-heal wounds. Our vision is to use the antimicrobial
effect in other areas of application where treatment with
conventional methods leads to unsatisfactory results. If several
hundred thousand patients die from VAP every year, this is
unacceptable. As a first mover, we are therefore systematically
driving forward the relevant research and striving to obtain
special approval for our PulmoPlas device as quickly as possible,
as we see an urgent medical need for a better solution to the VAP
problem. At the same time, we are tapping into an attractive market
segment, as the global market for mechanical ventilation is
predicted to see solid growth averaging 8.2% per year until 2032
due to the increase in chronic respiratory diseases."
Since October 2023, the MHH, in cooperation with Viromed Medical
AG, has been investigating the safety profile of the use of cold
plasma in bacterial infections of the respiratory tract using
models of the respiratory mucosa. In particular, the focus is on
the potential of cold plasma to kill bacteria that have infected
the epithelium. In parallel, possibly associated inflammatory
reactions, possible changes in cell differentiation, cell death,
DNA damage as well as the therapeutic dose and the time window of
application are being investigated. In order to optimize the
effectiveness of different plasma compositions, their effectiveness
in connection with cell damage will be investigated differentially.
Due to promising preliminary results that have shown no damaging
effect on the airway epithelium, a second study is now starting in
parallel, which was originally planned for mid-2025. This will
expand the investigation of the safety profile of cold plasma on
alveolar epithelium, taking into account mechanical shear forces
that act on the alveolar mucosa during breathing. In addition, the
potential and safety of cold plasma to kill bacteria applied to
precision-cut lung slices (PCLS) will be tested.
Prof. Dr. Hortense Slevogt, Clinic for Pneumology and
Infectiology, MHH: "Ventilator-associated pneumonia not only
has a high mortality rate, it is also a general burden on the
healthcare system due to increased antibiotic consumption, longer
patient stays and higher treatment costs. The increasing antibiotic
resistance of pathogens also makes new, non-antibiotic approaches
urgently necessary. If the positive preliminary results of our
study continue to be confirmed and the safety of cold physical
plasma in the human lung is established, cold plasma has the
potential to revolutionize the treatment of ventilated
patients."
About Viromed Medical AG:
Viromed Medical AG has a broad customer base in the DACH region,
including various DAX companies, e.g. Volkswagen and Lufthansa, as
well as federal states and various federal ministries, 1,100
hospitals, 7,000 pharmacies, and 17,000 medical practices.
Language: English Company: Viromed Medical AG Flensburger Straße 18
25421 Pinneberg Germany Phone: +49 4101 809960 E-mail:
kontakt@viromed-medical.de Internet:
https://www.viromed-medical-ag.de/ ISIN: DE000A3MQR65 WKN: A3MQR6
Listed: Regulated Unofficial Market in Berlin, Dusseldorf, Hamburg
EQS News ID:
1942511
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version on businesswire.com: https://www.businesswire.com/news/home/20240709060458/en/
Uwe Perbandt CEO Email: kontakt@viromed-medical.de
www.viromed-medical-ag.de