Axogen Sponsored REPOSE℠ Study Completes Pilot Phase Analysis
Thursday, February 18, 2021
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Axogen Sponsored REPOSE℠ Study Completes Pilot Phase Analysis
Pilot study demonstrates clinically significant improvement for subjects with chronic neuropathic painALACHUA, Fla., Feb.
18, 2021 (GLOBE NEWSWIRE) -- Axogen, Inc. (NASDAQ: AXGN), a global
leader in developing and marketing innovative surgical solutions for
damage or transection to peripheral nerves, today announced completion
of pilot phase analysis for its REPOSE clinical study.
Analysis
of the REPOSE study’s 15-subject single arm pilot phase demonstrated
that subjects experienced a clinically significant reduction in pain
from baseline at each of the 3, 6, 9, and 12 month timepoints following
surgical excision of the neuroma and placement of Axoguard Nerve Cap®
(p<0.0001). Specifically, the study observed a mean reduction in
pain of 69 points at 3 months and 80 points at 12 months as measured on
the 100-point Visual Analog Scale (VAS). Additionally, subjects
experienced clinically meaningful improvements in Fatigue, Physical
Function, Sleep Disturbance, Pain Interference, Pain Intensity, and Pain
Behavior as measured by the validated PROMIS®
questionnaires, and pain medication utilization data showed positive
indicators for a reduction of pain medication burden, including opioids,
following the procedure. “Neuroma pain can be a
challenging clinical condition to manage, and results from historical
treatment options, both surgical and pharmacological, can be limited,”
said Craig Thomajan, DPM, FACFAS, FAENS, Peripheral Nerve Surgeon at
Austin Foot and Ankle Specialists, and the lead clinical investigator
for REPOSE. “We are pleased with the early successes from REPOSE and are
excited to continue this meaningful study. Access to impactful
technologies for the treatment and prevention of symptomatic neuromas
offers patients an opportunity for reduced pain and improved quality of
life.” “We are pleased that the analysis of this pilot phase
clinical data demonstrates the potential impact our Axoguard Nerve Cap
can have on symptomatic neuroma pain. The outcomes reinforce the
assumptions used in our study modeling and exceed those reported for
standard neurectomy,” said Karen Zaderej, chairman, CEO, and president.
“We believe the comparative phase of the study will support the role of
Axoguard Nerve Cap in the management of symptomatic neuroma. We continue
to be committed to providing surgeons with clinical evidence advancing
the science of nerve repair, including surgical treatments that provide
clinically meaningful improvements for patients suffering with chronic
nerve pain.” Enrollment in the comparative phase of REPOSE is
underway and the company expects enrollment to be completed in the first
quarter of 2022, assuming limited impact from COVID-19. About REPOSE A
Multicenter, Prospective, Randomized and Subject Blinded Comparative
Study of Axoguard Nerve Cap and Neurectomy for the Treatment of
Symptomatic Neuroma and Prevention of Recurrent End-Neuroma Pain
(REPOSE) is the company’s post-market study comparing placement of
Axoguard Nerve Cap to standard neurectomy alone for subjects with
symptomatic neuroma pain. The study design includes a 15 subject open
label pilot phase and up to 86 subjects in a randomized comparative
phase. The study requires a one year follow up period for all subjects
and is designed to assess changes in pain scores as measured by Visual
Analog Scale, quality of life outcomes, medication usage, and subject
satisfaction. About Axoguard Nerve Cap Axoguard
Nerve Cap is a porcine submucosa ECM product used to protect a
peripheral nerve end and separate the nerve from the surrounding
environment to reduce the development of symptomatic or painful neuroma.
Axoguard Nerve Cap provides protection for a peripheral nerve end or
stump where repair is unattainable or not desired. About Axogen Axogen
(AXGN) is the leading company focused specifically on the science,
development, and commercialization of technologies for peripheral nerve
regeneration and repair. Axogen employees are passionate about helping
to restore peripheral nerve function and quality of life to patients
with physical damage or transection to peripheral nerves by providing
innovative, clinically proven, and economically effective repair
solutions for surgeons and health care providers. Peripheral nerves
provide the pathways for both motor and sensory signals throughout the
body. Every day, people suffer traumatic injuries or undergo surgical
procedures that impact the function of their peripheral nerves. Physical
damage to a peripheral nerve, or the inability to properly reconnect
peripheral nerves, can result in the loss of muscle or organ function,
the loss of sensory feeling, or the initiation of pain. Axogen's platform for peripheral nerve repair features a comprehensive portfolio of products, including Avance®
Nerve Graft, a biologically active off-the-shelf processed human nerve
allograft for bridging severed peripheral nerves without the
comorbidities associated with a second surgical site; Axoguard®
Nerve Connector, a porcine submucosa extracellular matrix (ECM)
coaptation aid for tensionless repair of severed peripheral nerves;
Axoguard® Nerve Protector, a porcine submucosa ECM product
used to wrap and protect damaged peripheral nerves and reinforce the
nerve reconstruction while preventing soft tissue attachments; Axoguard
Nerve Cap®, a porcine submucosa ECM product used to protect a
peripheral nerve end and separate the nerve from the surrounding
environment to reduce the development of symptomatic or painful neuroma;
and Avive® Soft Tissue Membrane, a processed human umbilical
cord intended for surgical use as a resorbable soft tissue barrier. The
Axogen portfolio of products is available in the United States, Canada,
the United Kingdom, South Korea, and several other European and
international countries. Cautionary Statements Concerning Forward-Looking Statements This press
release contains “forward-looking” statements as defined in the Private
Securities Litigation Reform Act of 1995. These statements are based on
management's current expectations or predictions of future conditions,
events, or results based on various assumptions and management's
estimates of trends and economic factors in the markets in which we are
active, as well as our business plans. Words such as “expects,”
“anticipates,” “intends,” “plans,” “believes,” “seeks,” “estimates,”
“projects,” “forecasts,” “continue,” “may,” “should,” “will,” “goals,”
and variations of such words and similar expressions are intended to
identify such forward-looking statements. The forward-looking statements
may include, without limitation, statements related to the expected
impact of COVID-19 on our business, statements regarding our growth,
product development, product potential, financial performance, sales
growth, product adoption, market awareness of our products, data
validation, our assessment of our internal controls over financial
reporting, our visibility at and sponsorship of conferences and
educational events. The forward-looking statements are and will be
subject to risks and uncertainties, which may cause actual results to
differ materially from those expressed or implied in such
forward-looking statements. Forward-looking statements contained in this
press release should be evaluated together with the many uncertainties
that affect our business and our market, particularly those discussed
under Part I, Item 1A., “Risk Factors,” of our Annual Report on Form
10-K, as amended on Form 10-K/A, for the fiscal year ended December 31,
2019, as well as other risks and cautionary statements set forth in our
filings with the U.S. Securities and Exchange Commission.
Forward-looking statements are not a guarantee of future performance,
and actual results may differ materially from those projected. The
forward-looking statements are representative only as of the date they
are made and, except as required by applicable law, we assume no
responsibility to publicly update or revise any forward-looking
statements, whether as a result of new information, future events,
changed circumstances, or otherwise. Contact: Axogen, Inc. Peter Mariani, Chief Financial Officer [email protected]
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