Corporate News
Xenon MRI System trade-in agreement entered with the University of Virginia Health Hospital
19 July 2024
Polarean Imaging plc (AIM: POLX), a commercial-stage medical device leader in advanced
Magnetic Resonance Imaging ("MRI") of lung function, announces that it has entered into
a trade-in agreement to exchange the University of Virginia Health System’s (“UVA
Health”) existing two research hyperpolarisers for two new clinical-grade hyperpolariser
systems to be provided by Polarean.
UVA Health is an integrated health system with a world-class academic medical center that
includes a Level 1 Trauma Centre, an NCI-designated Comprehensive Cancer Center, and UVA
Health Children’s, the number one pediatric hospital in Virginia. UVA Health’s
Hyperpolarized Gas MR Imaging Center faculty pioneered the application of Xenon MRI for
a variety of lung diseases, including asthma, cystic fibrosis, and bronchopulmonary
dysplasia.
Replacing these research hyperpolarisers is the first step to UVA Health advancing its
leadership position in the Mid-Atlantic as a centre of excellence for NIH grants,
industry-sponsored trials, and clinical patient referrals for this novel imaging
modality. Polarean expects to install the new systems later this year and will
collaborate closely with UVA Health to ensure a successful implementation that enhances
the Xenon MRI research program and establishes the foundation for clinical Xenon MRI
capabilities.
Christopher von Jako, Ph.D, CEO of Polarean, said: “We are delighted to see UVA
Health upgrade both of their hyperpolariser systems to clinical grade. This
milestone underscores the increasing adoption of Polarean’s technology and the
continued progress in our strategy to convert previously research-only centres to
clinical-grade, in addition to establishing de novo sites. We look forward to
working with the team at UVA Health to ensure that their implementation of our Xenon
MRI technology is successful as it continues to advance research and move
into clinical use.”
This announcement contains inside information for the purposes of Article 7 of Regulation (EU) 596/2014, as it forms part of domestic law by virtue of the European Union (Withdrawal) Act 2018.
Enquiries:
Polarean Imaging plc | www.polarean.com / www.polarean-ir.com | |||||
Christopher von Jako, Ph.D, Chief Executive Officer | Via Walbrook PR | |||||
Charles Osborne, Chief Financial Officer | ||||||
Stifel Nicolaus Europe Limited (NOMAD and Sole Corporate Broker) | +44 (0)20 7710 7600 | |||||
Nicholas Moore / Samira Essebiyea / Kate Hanshaw (Healthcare Investment Banking) | ||||||
Nick Harland (Corporate Broking) | ||||||
Walbrook PR | Tel: +44 (0)20 7933 8780 or [email protected] | |||||
Anna Dunphy / Phillip Marriage | Mob: +44 (0)7876 741 001 / +44 (0)7867 984 082 |
About Polarean
Polarean is a revenue-generating medical imaging technology company revolutionising
pulmonary medicine through direct visualisation of lung function by introducing the
power and safety of MRI to the respiratory healthcare community. This community is in
desperate need of modern solutions to accurately assess lung function. The Company
strives to optimise lung health and prevent avoidable loss by illuminating hidden
disease, addressing the global unmet medical needs of more than 500 million patients
worldwide suffering from chronic respiratory disease. Polarean is a leader in the field
of hyperpolarisation science and has successfully developed the first and only
hyperpolarised Xenon MRI inhaled contrast agent, XENOVIEW™, which is now FDA-approved in
the United States. Polarean is dedicated to researching, developing, and commercialising
innovative imaging solutions with its non-invasive and radiation-free pulmonary
functional MRI platform. This comprehensive drug-device platform encompasses the
proprietary Xenon gas blend, gas hyperpolarisation system, as well as software and
accessories, facilitating fully integrated modern respiratory imaging operations.
Founded in 2012, with offices in Durham, NC, and London, United Kingdom, Polarean is
committed to increasing global awareness of and broad access to its XENOVIEW MRI
technology platform. For the latest news and information about Polarean, please
visit www.polarean.com.
XENOVIEW IMPORTANT SAFETY INFORMATION
Indication
XENOVIEW™, prepared from the Xenon Xe 129 Gas Blend, is a hyperpolarized contrast agent
indicated for use with magnetic resonance imaging (MRI) for evaluation of lung
ventilation in adults and pediatric patients aged 12 years and older.
Limitations of Use
XENOVIEW has not been evaluated for use with lung perfusion imaging.
CONTRAINDICATIONS
None.
Warnings and Precautions
Risk of Decreased Image Quality from Supplemental Oxygen: Supplemental oxygen
administered simultaneously with XENOVIEW inhalation can cause degradation of image
quality. For patients on supplemental oxygen, withhold oxygen inhalation for two breaths
prior to XENOVIEW inhalation, and resume oxygen inhalation immediately following the
imaging breath hold.
Risk of Transient Hypoxia: Inhalation of an anoxic gas such as XENOVIEW may cause
transient hypoxemia in susceptible patients. Monitor all patients for oxygen
desaturation and symptoms of hypoxemia and treat as clinically indicated.
Adverse Reactions
Adverse Reactions in Adult Patients: The adverse reactions (> one patient) in efficacy trials were oropharyngeal pain, headache, and dizziness. Adverse Reactions in Pediatric and Adolescent Patients: In published literature in pediatric patients aged 6 to 18, transient adverse reactions were reported: blood oxygen desaturation, heart rate elevation, numbness, tingling, dizziness, and euphoria. In at least one published study of pediatric patients aged 6 to 18 years, transient decrease in SpO2% and transient increase in heart rate was reported following hyperpolarized xenon Xe 129 administration. XENOVIEW is not approved for use in pediatric patients less than 12 years of age.
Please see full prescribing information at www.XENOVIEW.netLatest News
- Holding(s) in Company
11 September 2025 - Submission of new Phase III study protocol to FDA for expanded
indication of XENOVIEW
12 August 2025 - Block Listing Six Monthly Return
24 July 2025
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