11 November
2024
AOTI, INC. (the "Company" or
"Group" or "AOTI")
CMS commences formal review
for Topical Oxygen Therapy coverage
AOTI, INC. (AIM: AOTI), a medical
technology group focussed on the durable healing of wounds and
prevention of amputations, is pleased to note that the Centers for
Medicare and Medicaid Services (CMS), through its Durable Medical
Equipment (DME) Medicare Administrative Contractors (MACs), has
scheduled a public Contractor Advisory Committee (CAC) meeting. The
CAC meeting on 11 December 2024 will convene subject matter experts
to consider revising the Oxygen and Oxygen Equipment Local Coverage
Determination (LCD) to include language indicating that Topical
Oxygen is reasonable and necessary for wound healing
therapy.
The
specialty focused CAC meeting is to discuss the scientific evidence
underlying the requested LCD and to provide a formal mechanism for
healthcare professionals to be informed of the evidence used in
developing the LCD and promote communications between the
DME MACs and the
healthcare community. During the
meeting, the CAC members will be asked to
discuss the clinical literature related to the LCD reconsideration
request and to score a series of key questions that will help guide
CMS in drafting their proposed LCD revision. The DME MACs will then
publish the proposed LCD and generally have up to 365 calendar days
from the publication date to finalise the process.
Dr.
Mike Griffiths, Chief Executive Officer and President of AOTI,
INC., commented: "Following the specialist
led coverage reconsideration request made in mid-2023, we are
delighted that CMS has decided to initiate their coverage review of
topical oxygen therapy. Such coverage, if achieved, would provide
significant additional momentum to accelerate our business
trajectory above what we have outlined previously, and provide us
with access to the c.65 million Americans covered by Medicare (the
Government-funded healthcare insurance scheme for citizens 65 years
of age and over).
"Our unique topical wound oxygen (TWO2®) therapy has revolutionised
chronic wound healing, by providing significant reductions in wound
related reoccurrence, hospitalisations and
amputations1,2. AOTI is proud to continue its efforts to
expand the access of these benefits to all patients, predominately
applied in their homes, thereby driving meaningful improvements in
access-to-care for those who need it most."
1.
Multinational, Multicenter, Randomized, Double-Blinded,
Placebo-Controlled Trial to Evaluate the Efficacy of Cyclical
Topical Wound Oxygen (TWO2) Therapy in the Treatment of Chronic
Diabetic Foot Ulcers; The TWO2 Study. Robert G. Frykberg et al,
Diabetics Care 2020; 43:616-624. https://doi.org/10.2337/dc19-0476
2.
Reduced Hospitalizations and Amputations in Patients with Diabetic
Foot Ulcers Treated with Cyclical Pressurized Topical Wound Oxygen
Therapy: Real-World Outcomes; Jessica Izhakoff Yellin, et al;
Advances in Wound Care 2022; http://doi.org/10.1089/wound.2021.0118
END
AOTI, INC.
Dr. Mike Griffiths, Chief Executive
Officer
Jayesh Pankhania, Chief Financial
Officer
|
+44 (0)20 3727 1000
ir@aotinc.net
|
Peel Hunt LLP (Nominated Adviser and Broker)
Dr. Christopher Golden, Patrick
Birkholm
|
+44 (0)20 7418 8900
|
FTI
Consulting (Financial PR & IR)
Ben Atwell, Simon Conway,
Natalie Garland-Collins, Alex
Davis
|
+44 (0)20 3727 1000
AOTI@fticonsulting.com
|
ABOUT AOTI, INC.
AOTI, INC. was founded in 2006 and
is based in Oceanside, California, US and Galway, Ireland,
providing innovative solutions to resolve severe and chronic wounds
worldwide. Its products reduce healthcare costs and improve the
quality of life for patients with these debilitating conditions.
The Company's patented non-invasive Topical Wound Oxygen
(TWO2®) therapy has demonstrated in
differentiating, robust, double-blinded randomised controlled
trials (RCT) and real-world evidence (RWE) studies to more-durably
reduce the recurrence of Diabetic Foot Ulcers (DFUs), resulting in
an unprecedented 88 per cent reduction in hospitalisations and 71
per cent reduction in amputations over 12 months.
TWO2® therapy can be administered by the
patient at home, improving access to care and enhancing treatment
compliance. TWO2® therapy has received
regulatory clearance from the US (FDA), Europe (CE Mark), UK
(MHRA), Health Canada, the Chinese National Medical Products
Administration, Australia (TGA) and in Saudi Arabia. Also
see www.aotinc.net