Axogen Announces Appointment of Jesse Bishop as Vice President of Regulatory Affairs and Inducement Grant Under Nasdaq Listing Rule 5635(c)(4)
February 03 2025 - 8:00AM
Axogen, Inc. (NASDAQ: AXGN), a global leader in developing and
marketing innovative surgical solutions for peripheral nerve
injuries, today announced the appointment of Jesse Bishop as Vice
President of Regulatory Affairs.
Mr. Bishop will report to Michael Dale, President, and Chief
Executive Officer, and will lead the development and execution of
domestic and international regulatory strategies to advance company
objectives related to new product development, market approval,
market development and other regulatory initiatives.
Mr. Bishop will oversee all facets of Axogen’s regulatory
affairs, maintenance of Axogen product registrations, licenses,
accreditations and in general all related interactions and
relationships with regulatory agencies and associated stakeholders.
Additionally, Mr. Bishop will be responsible for working on
development of regulatory policy with external groups such as
Alliance for Regenerative Medicine (ARM), American Association of
Tissue Banks (AATB) and others.
Mr. Bishop brings extensive experience in leading regulatory
strategy and CMC, CGMP manufacture of cell and gene therapies,
biologics/vaccines, medical devices and combination products. Mr.
Bishop has over 13 years of leadership experience in regulatory
strategy, planning and execution in companies such as Thermo Fisher
Scientific – Viral Vector Services, RGI Medical Manufacturing,
Ology Bioservices and Lacerta Therapeutics. He also served in the
military as a Ranger Team Leader and Combat Medic within U.S. Army
Special Operations.
Mr. Bishop earned his master’s in medical sciences and business
administration from the University of Florida.
“We are pleased to welcome Jesse to the Axogen team," said
Michael Dale, Chief Executive Officer, and Director, Axogen. "His
extensive experience in regulatory strategy and deep understanding
of the biologics and medical device sectors will be valuable as we
continue to advance our regulatory initiatives and expand our
product portfolio.”
Jesse Bishop, Vice President of Regulatory Affairs, said: “I am
honored to join Axogen and contribute to advancing the regulatory
pathway for peripheral nerve repair technologies."
Notice of Issuance of Inducement Grant
In connection with the commencement of his employment on
February 3, 2025, and as a material inducement of employment, Mr.
Bishop will be awarded an equity grant on March 3, 2025, consisting
of non-qualified equity grant in the form of Restricted Stock Units
(RSU) for the grant of 45,000 shares of Axogen, Inc. common stock.
The shares representing the RSUs are subject to vesting over 4
years, with 50% vesting after the second year and 25% of the total
shares granted vesting every year thereafter for the next two
years.
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 that are used across two
primary application categories: scheduled, non-trauma procedures
and emergent trauma procedures. Scheduled procedures are generally
characterized as those where a patient is seeking relief from
conditions caused by a nerve defect or surgical procedure. These
procedures include providing sensation for women seeking breast
reconstruction following a mastectomy, nerve reconstruction
following the surgical removal of painful neuromas, oral and
maxillofacial procedures, and nerve decompression. Emergent
procedures are generally characterized as procedures resulting from
injuries that initially present in an ER. These procedures are
typically referred to and completed by a specialist either
immediately or within a few days following the initial injury.
Axogen’s product portfolio includes 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 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 HA+ Nerve Protector™, a porcine
submucosa ECM base layer coated with a proprietary
hyaluronate-alginate gel, a next-generation technology designed to
provide short- and long-term protection for peripheral nerve
injuries; and 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. The Axogen portfolio of products is
available in the United States, Canada, Germany, the United
Kingdom, Spain, South Korea, and several other countries.
Investor Contact:Axogen, Inc.
InvestorRelations@axogeninc.com
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