Aetna Policy Update Expands TMS Availability for Adolescents With Depression
July 22 2024 - 8:31AM
Neuronetics, Inc. (NASDAQ: STIM), a medical technology company
focused on designing, developing, and marketing products that
improve the quality of life for patients who suffer from
neurohealth disorders, announced that Aetna has updated its TMS
(transcranial magnetic stimulation) coverage to include adolescents
aged 15 and older with MDD (major depressive disorder). This
expanded access follows the recent clearance from the U.S. Food and
Drug Administration (FDA) for NeuroStar TMS as the first and only
TMS treatment cleared as a first-line add-on for adolescents aged
15-21.
The coverage criteria specify that TMS treatment must be
administered by an FDA-cleared device in accordance with FDA
labeled indications. Aetna is one of the largest health plans in
the country with over 19.4 million lives covered through its
commercial policies nationwide. The TMS policy update is effective
immediately.
“We commend Aetna for being a leader among payors in recognizing
the critical need to reduce barriers to proven treatments for
adolescent mental health,” stated Keith J. Sullivan, President and
CEO of Neuronetics, Inc. “Enabling earlier access to NeuroStar TMS
as part of an individual’s care plan is a significant step payors
can take toward helping to mitigate the mental health crisis
affecting young people.”
This policy update builds on recent momentum from both
commercial and government payers to expand adolescent coverage for
TMS Therapy. Neuronetics previously announced updated policies
through payers such as Medi-Cal and Humana. In addition to being
the first and only TMS company with FDA clearance for adolescent
treatment, Neuronetics is the only TMS company in the industry with
a dedicated health policy team that partners with both providers
and payors to advocate for health policy updates.
For more information about NeuroStar TMS Therapy, please
visit www.neurostar.com.
About Adolescent DepressionAdolescent
depression is a complex and challenging mental health condition
that affects young individuals during the crucial period of
adolescence. An estimated 4.3 million U.S. adolescents aged 15-21
are affected by MDDi. Depression amongst adolescents can disrupt
crucial aspects of development, such as academic performance,
relationships with peers and family members, and overall emotional
well-being.
NeuroStar Advanced Therapy is indicated as an adjunct for the
treatment of MDD in adolescent patients aged 15-21.
About NeuroneticsNeuronetics,
Inc. believes that mental health is as important as physical
health. As a global leader in
neuroscience, Neuronetics is redefining patient and
physician expectations with its NeuroStar Advanced Therapy for
Mental Health. NeuroStar is a non-drug, noninvasive treatment that
can improve the quality of life for people suffering from
neurohealth conditions when traditional medication hasn’t helped.
NeuroStar is indicated for the treatment of depressive episodes and
for decreasing anxiety symptoms for those who may exhibit comorbid
anxiety symptoms in adult patients suffering from MDD and who
failed to achieve satisfactory improvement from previous
antidepressant medication treatment in the current episode. It is
also FDA-cleared as an adjunct for adults with obsessive-compulsive
disorder and for adolescent patients aged 15-21 with MDD. NeuroStar
Advanced Therapy is the leading TMS treatment for MDD in adults
with over 6.4 million treatments delivered. Neuronetics is
committed to transforming lives by offering an exceptional
treatment that produces extraordinary results. For safety and
prescribing information,
visit www.neurostar.com.
Media
Contact:EvolveMKD646.517.4220NeuroStar@evolvemkd.com
iWorld Health Organization, Depression Fact Sheet.
https://www.who.int/news-room/fact-sheets/detail/depression.
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