Next Science Begins U.S. Clinical Trial for XPERIENCE No Rinse Antimicrobial Solution
August 11 2021 - 10:54AM
Business Wire
Highlights
- Clinical trial for XPERIENCE commences after receiving FDA
clearance in April
- Randomized, controlled, double-blinded study will evaluate the
effects of XPERIENCE in decreasing surgical site infections
- Study will focus on patients undergoing tibial fracture
repair
Next Science Limited (ASX:NXS) (Next Science / Company)
is pleased to announce that a clinical trial has been initiated in
the U.S. for XPERIENCE TM No Rinse Antimicrobial Solution.
Enrollment in the 30-patient, 90-day study is currently
underway.
The trial, the TIFRAX (Tibial Fracture) Study, is a randomized,
controlled, double-blinded, prospective study to evaluate the
efficacy of XPERIENCE in helping decrease wound bioburden and
surgical site infections (SSI). It will also evaluate whether
XPERIENCE can improve post-operative outcomes when used as adjunct
treatment to standard of care in patients undergoing tibial
fracture repair.
The study’s primary investigator is Dr. Robert Harris, an
orthopaedic trauma surgeon with the Hughston Clinic in Columbus,
Georgia. In addition to serving as the director of orthopaedic
trauma for the Hughston Clinic, Dr. Harris is a fellow of the
American Academy of Orthopaedic Surgeons and a member of several
orthopaedic surgery associations, including the American
Orthopaedic Association, the Orthopaedic Trauma Association and the
Society of Military Orthopaedic Surgeons.
XPERIENCE is a no-rinse solution that is designed to help
prevent surgical site and post-operative infections by rinsing away
debris and microorganisms. XPERIENCE breaks down biofilms, which
are powerful communities of bacteria that function as a single
entity with behaviors and defenses that are a leading contributor
to SSIs.1 2 Biofilms account for more than 80% of microbial
infections in the human body,3 according to the U.S. National
Institutes of Health.
“The start of this trial is a significant milestone in the
clinical development of XPERIENCE and for the evolution of our
company,” said Managing Director Judith Mitchell. “Next Science has
a unique opportunity to change the trajectory of the war on
infection by providing solutions that eliminate biofilms, and their
incumbent bacteria. The results of this clinical trial will help in
the global fight against surgical site infections, which in the
U.S. alone contribute an additional $3.5 billion annually to the
cost of healthcare.4”
In April, Next Science announced it had received 510(k)
clearance from the Food and Drug Administration for the sale of
XPERIENCE as a medical device in the U.S. XPERIENCE is
predominantly used in orthopaedic procedures, including shoulder,
hip, knee, trauma and podiatry surgeries. Future studies will look
at expanding current indications.
XPERIENCE is the newest innovative product from Next Science,
whose mission is to heal patients and save lives by addressing the
impact of biofilms on human health. Each of these products is
powered by XBIO™ Technology, which disrupts biofilm’s extracellular
polymeric substance and makes the bacteria within the biofilm more
vulnerable to attack.
About Next Science
Next Science is a medical technology company headquartered in
Sydney, Australia, with a research and development center in
Florida, USA. Established in 2012, the Company’s primary focus is
on the development and continued commercialization of products
powered by its proprietary XBIO Technology to reduce the impact of
biofilm-based infections in human health. XBIO is a unique,
non-toxic technology with proven efficacy in eradicating both
biofilm-based and free-floating bacteria. For further information
visit: www.nextscience.com.
Forward-looking statements
This announcement may contain forward-looking statements which
may be identified by words such as “believes”, “considers”,
“could”, “estimates”, “expects”, “intends”, “may”, and other
similar words that involve risks and uncertainties. Such statements
are not guarantees of future performance and involve known and
unknown risks, uncertainties, assumptions and other important
factors, many of which are beyond the control of Next Science or
its Directors and management, and could cause Next Science’s actual
results and circumstances to differ materially from the results and
circumstances expressed or anticipated in these statements. The
Directors cannot and do not give any assurance that the results,
performance or achievements expressed or implied by the
forward-looking statements contained in this announcement will
actually occur and investors are cautioned not to place undue
reliance on these forward-looking statements.
1 International Wound Infection Institute (IWII) Wound infection
in clinical practice. Wounds International. 2 Hall-Stoodley L,
Stoodley P. Evolving concepts in biofilm infections. Cell
Microbiol. 2009;11(7):1034-43. 3 Joo HS, Otto M. Molecular basis of
in-vivo biofilm formation by bacterial pathogens. Chemistry &
Biology. 2012;19(12):1503-1513. 4 Zimlichman, E., et al., “Health
Care-Associated Infections. A Meta-analysis of Costs and Financial
Impact on the US Health Care System”. JAMA Intern Med, 173(22):
(2013): 2039-46.
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Judith Mitchell Managing Director, Next Science Limited
Phone: +61 2 9375 7989 Email: investorqueries@nextscience.com
Michael Brown Pegasus Advisory Phone: +61 400 248 080
Email: mbrown@pegasusadvisory.com.au
Anthony Priwer Dalton Agency Phone: +1 615.515.4891
Email: apriwer@daltonagency.com
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