Hyperfine, Inc. Takes the Stage at ISMRM with Seventeen Abstracts Assessing the Potential of Using Swoop® System Images Across Multiple Care Settings and Clinical Conditions
April 23 2024 - 9:00AM
Business Wire
Data on the company’s portable MR imaging
system show it can acquire brain images at the point of care that
may assist physicians with screening and monitoring for Alzheimer’s
and multiple sclerosis biomarkers
Hyperfine, Inc. (Nasdaq: HYPR), the groundbreaking health
technology company that has redefined brain imaging with the first
FDA-cleared portable magnetic resonance (MR) brain imaging
system—the Swoop® system—today announced the acceptance of
seventeen ultra-low-field MRI-related abstracts that will be
presented at the 2024 International Society for Magnetic Resonance
in Medicine (ISMRM) annual meeting, being held from May 4–9 in
Singapore. These seventeen abstracts span a wide variety of use
cases, including two that highlight the utility of brain images
acquired with the ultra-low-field Swoop® Portable MR Imaging®
system to aid physicians screening for various biomarkers and
monitoring disease progression unique to neurodegenerative
diseases, including Alzheimer’s and multiple sclerosis (MS).
Conference attendees can learn more during these select
presentations:
Title: Unpaired Image-to-Image Translation of ULF-MRI
using Vision Transformers to Advance Volumetric Analyses
Authors: Peter Hsu et al. Session: Power Pitch:
AI-Empowered Image Analysis & Processing (PP-25) Date and
time: Thursday, May 9, 8:15–9:15 AM SGT Location: Power
Pitch Theater 1
Title: Subtraction Map Pipeline to Assess Longitudinal
Changes in Multiple Sclerosis at Portable Ultra-Low Field MRI
Authors: Corinne Donnay et al. Session: Digital
Poster: Emerging Methods for Imaging Multiple Sclerosis I (D-128)
Date and time: Tuesday, May 7, 3:45–4:45 PM SGT
Location: Exhibition Hall (Hall 403)
“These abstracts are very encouraging. The scientific and
clinical data supports the potential of portable ultra-low-field MR
imaging to assist physicians screening for and monitoring
neurodegenerative diseases like Alzheimer’s and MS,” said Maria
Sainz, President and CEO of Hyperfine, Inc. “The data shows that
ultra-low-field Swoop® system images can effectively help
physicians track a patient’s disease progression and highlights the
transformative and vast opportunity that fits the unique
characteristics of our portable imaging system, which can be
readily available across healthcare and resource settings.”
Hyperfine, Inc. is committed to delivering clinical value across
the continuum of care for patients suffering from some of the
largest and most devastating neurodegenerative diseases like
Alzheimer’s and MS and improving the complex treatment and care
management cycle many patients face. Earlier this month, the
company announced that the first patients have been scanned in the
CARE PMR (Capturing ARIA Risk Equitably with Portable MR) study.
The observational study assesses the clinical utility and workflow
benefits of acquiring the Swoop® system images at infusion centers
and clinics to help physicians detect amyloid-related imaging
abnormalities (ARIA) in Alzheimer’s patients receiving
amyloid-targeting therapy.
For more information about the Swoop® Portable MR Imaging®
system, please visit hyperfine.io.
About the Swoop® Portable MR Imaging® System
The Swoop® Portable MR Imaging® system is U.S. Food and Drug
Administration (FDA) cleared for brain imaging of patients of all
ages. It is a portable, ultra-low-field magnetic resonance imaging
device for producing images that display the internal structure of
the head where full diagnostic examination is not clinically
practical. When interpreted by a trained physician, these images
provide information that can be useful in determining a diagnosis.
The Swoop® system also has CE certification in the European Union
and UKCA certification in the United Kingdom. The Swoop® system is
commercially available in a select number of international
markets.
About Hyperfine, Inc.
Hyperfine, Inc. (Nasdaq: HYPR) is the groundbreaking health
technology company that has redefined brain imaging with the Swoop®
system—the first FDA-cleared, portable, ultra-low-field, magnetic
resonance brain imaging system capable of providing imaging at
multiple points of care. The mission of Hyperfine, Inc. is to
revolutionize patient care globally through transformational,
accessible, clinically relevant diagnostic imaging. Founded by Dr.
Jonathan Rothberg in a technology-based incubator called
4Catalyzer, Hyperfine, Inc. scientists, engineers, and physicists
developed the Swoop® system out of a passion for redefining brain
imaging methodology and how clinicians can apply accessible
diagnostic imaging to patient care. For more information, visit
hyperfine.io.
Hyperfine, Swoop, and Portable MR Imaging are registered
trademarks of Hyperfine, Inc.
Forward-Looking Statements
This press release includes “forward-looking statements” within
the meaning of the “safe harbor” provisions of the Private
Securities Litigation Reform Act of 1995. Actual results of
Hyperfine, Inc. (the “Company”) may differ from its expectations,
estimates and projections and consequently, you should not rely on
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Words such as “expect,” “estimate,” “project,” “budget,”
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performance and its ability to implement its strategy. These
forward-looking statements involve significant risks and
uncertainties that could cause the actual results to differ
materially from the expected results. Most of these factors are
outside of the Company’s control and are difficult to predict.
Factors that may cause such differences include, but are not
limited to: the success, cost and timing of the Company’s product
development and commercialization activities, including the degree
that the Swoop® system is accepted and used by healthcare
professionals; the impact of COVID-19 on the Company’s business;
the inability to maintain the listing of the Company’s Class A
common stock on the Nasdaq; the Company’s inability to grow and
manage growth profitably and retain its key employees; changes in
applicable laws or regulations; the inability of the Company to
raise financing in the future; the inability of the Company to
obtain and maintain regulatory clearance or approval for its
products, and any related restrictions and limitations of any
cleared or approved product; the inability of the Company to
identify, in-license or acquire additional technology; the
inability of the Company to maintain its existing or future
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obtain adequate supply of its products; the inability of the
Company to compete with other companies currently marketing or
engaged in the development of products and services that the
Company is currently marketing or developing; the size and growth
potential of the markets for the Company’s products and services,
and its ability to serve those markets, either alone or in
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the Company’s products and services; the Company’s estimates
regarding expenses, revenue, capital requirements and needs for
additional financing; the Company’s financial performance; and
other risks and uncertainties indicated from time to time in
Company’s filings with the Securities and Exchange Commission,
including those under “Risk Factors” therein. The Company cautions
readers that the foregoing list of factors is not exclusive and
that readers should not place undue reliance upon any
forward-looking statements, which speak only as of the date made.
The Company does not undertake or accept any obligation or
undertaking to release publicly any updates or revisions to any
forward-looking statements to reflect any change in its
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Media Contact Shay Smith Health+Commerce
shay@healthandcommerce.com
Investor Contact Marissa Bych Gilmartin Group LLC
marissa@gilmartinir.com
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