KORU Medical Systems Signs Supply Agreement for a Phase III Clinical Trial for a Novel Endocrinological Biologic
14 Maggio 2024 - 10:05PM
Business Wire
KORU Medical Systems, Inc. (NASDAQ: KRMD) (“KORU Medical” or
the “Company”), a leading medical technology company focused on
development, manufacturing, and commercialization of innovative and
patient-centric large volume subcutaneous infusion solutions, is
pleased to announce the signing of a Phase III clinical supply
agreement for a novel enzyme replacement therapy to treat a rare
endocrinological disease.
This significant milestone marks the progression of this
collaboration, previously announced in July 2023. Since then, the
KORU Medical Freedom System successfully passed validation testing
to meet the subcutaneous infusion administration specifications for
this novel drug. The Phase III trial will evaluate bi-weekly
infusions using the Freedom System. If successful in the Phase III
trial, this drug would be the first disease-modifying treatment
option for the 10,000 patients worldwide afflicted by this rare
genetic disease. The drug has been granted Breakthrough Therapy,
Rare Pediatric Disease, and Fast Track designations by the FDA, as
well as Orphan Drug designation in the US and Europe.
“We are proud of our role in developing devices that meet large
volume subcutaneous delivery needs in collaboration with our valued
pharmaceutical partners,” said Linda Tharby, President and CEO of
KORU Medical Systems. “With the start of this Phase III clinical
trial, we look forward to continuing to demonstrate our capability
to successfully administer rare disease drugs across a growing
range of indications.”
About KORU Medical Systems
KORU Medical Systems develops, manufactures, and commercializes
innovative and patient-centric large volume subcutaneous infusion
solutions that improve quality of life for patients around the
world. The FREEDOM Syringe Infusion System (the “Freedom System”)
currently includes the FREEDOM60® and FreedomEdge® Syringe Infusion
Drivers, Precision Flow Rate Tubing™ and HIgH-Flo Subcutaneous
Safety Needle Sets™. These devices are used for infusions
administered in the home and alternate care settings. For more
information, please visit www.korumedical.com.
Forward Looking Statements
This press release contains forward-looking statements within
the meaning of the Private Securities Litigation Reform Act of 1995
that involve risks and uncertainties, including but not limited to
those relating to the start of the Phase III clinical trial and the
use of the Freedom System in the clinical trial. Actual results may
differ materially from these statements due to potential risks and
uncertainties such as, among others, success of the clinical trial,
and by those risks and uncertainties included under the captions
"Risk Factors" in our Annual Report on Form 10-K for the year ended
December 31, 2023, which is on file with the SEC and available on
our website at www.korumedical.com/investors and on the SEC website
at www.sec.gov. All information provided in this release and in the
attachments is as of May 14, 2024. Undue reliance should not be
placed on the forward-looking statements in this press release,
which are based on information available to us on the date hereof.
We undertake no duty to update this information unless required by
law.
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version on businesswire.com: https://www.businesswire.com/news/home/20240514305737/en/
Investor Contact: Louisa Smith
investor@korumedical.com
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