Santhera Enters into Supply and Distribution Agreement for AGAMREE® (Vamorolone) with Clinigen Group
January 06 2025 - 1:00AM
Pratteln, Switzerland, January 6, 2025 –
Santhera Pharmaceuticals (SIX: SANN) announces the signing of an
exclusive agreement with Clinigen Group to manage the supply and
distribution of AGAMREE® (vamorolone) in countries where the
product is not otherwise commercially available.
Santhera Pharmaceuticals and Clinigen Group
announce that they have signed a Supply and Distribution Agreement
for AGAMREE in countries where the product can currently not be
commercially obtained via Santhera or one of its current
distribution partners. The agreement will enable access to AGAMREE
on a case-by-case basis for patients with Duchenne muscular
dystrophy (DMD) in situations where the treating physician deems
there to be no suitable alternatives and where regulations allow
for it. This agreement allows Santhera to receive the majority
share of revenue generated from the supply of product in these
additional countries.
“This distribution agreement with Clinigen,
which is complementary to other, earlier announced, partnerships
and agreements, will allow Santhera to significantly increase our
service level to patients and healthcare professionals through
processing individual requests for AGAMREE from geographies in
which Santhera is not directly represented or while negotiations
with local partners are ongoing,” said Geert Jan van Daal,
MD, PhD, Chief Commercial Officer of Santhera.
“DMD is one of the most common and devastating
types of muscular degeneration, it is a progressive condition
diagnosed in childhood and it is encouraging to be able to help
healthcare professionals support appropriate patients with an
additional treatment option. We look forward to working with
Santhera to make AGAMREE available to patients globally on an
unlicensed basis in those territories where it is not currently
licensed or reimbursed. This partnership demonstrates our ongoing
commitment to accelerate access to medicines, to improve the
quality of people’s lives around the world,” said Julie
Gosper, Senior Vice President, Europe and Partner Markets at
Clinigen.
In addition to opening this distribution
channel, Santhera continues its gradual rollout of AGAMREE in key
European geographies. Commercialization of AGAMREE in Germany and
Austria, where the reception has been very positive, started in
Q1-2024. Santhera plans to launch AGAMREE in Europe's other major
markets, with the UK (including Scotland) in early 2025. The
rollout will continue throughout 2025 across France, Italy, Spain,
and other European countries. Santhera continues to expand its
partner network, which already includes multiple geographies, to
bring AGAMREE to patients with DMD in need of treatment.
About AGAMREE®
(vamorolone)AGAMREE (vamorolone), an orphan medicinal
product, is approved for use in the United States (Prescribing
Information), the European Union (Summary of Product
Characteristics), the United Kingdom, Mainland China and Hong
Kong.
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(2022). JAMA Neurol. 2022;79(10):1005-1014.
doi:10.1001/jamaneurol.2022.2480. Link.[3]
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(2019). Life Science Alliance DOI: 10.26508[5]
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2022, FP.27 - Poster 71.
Link.[6] Hasham et
al., MDA 2022 Poster presentation. Link.
About Duchenne Muscular
Dystrophy Duchenne muscular dystrophy (DMD) is a rare
inherited X-chromosome-linked disease, which almost exclusively
affects males. DMD is characterized by inflammation which is
present at birth or shortly thereafter. Inflammation leads to
fibrosis of muscle and is clinically manifested by progressive
muscle degeneration and weakness. Major milestones in the disease
are the loss of ambulation, the loss of self-feeding, the start of
assisted ventilation, and the development of cardiomyopathy. DMD
reduces life expectancy to before the fourth decade due to
respiratory and/or cardiac failure. Corticosteroids are the current
standard of care for the treatment of DMD.
About SantheraSanthera
Pharmaceuticals (SIX: SANN) is a Swiss specialty pharmaceutical
company focused on the development and commercialization of
innovative medicines for rare neuromuscular diseases with high
unmet medical need. The Company has an exclusive license from
ReveraGen for all indications worldwide to AGAMREE® (vamorolone), a
dissociative steroid with novel mode of action, which was
investigated in a pivotal study in patients with Duchenne muscular
dystrophy (DMD) as an alternative to standard corticosteroids.
AGAMREE for the treatment of DMD is approved in the U.S. by the
Food and Drug Administration (FDA), in the EU by the European
Medicines Agency (EMA), in the UK by the Medicines and Healthcare
products Regulatory Agency (MHRA), in China by the National Medical
Products Administration (NMPA) and Hong Kong by the Department of
Health (DoH). Santhera has out-licensed rights to AGAMREE for North
America to Catalyst Pharmaceuticals and for China and certain
countries in Southeast Asia to Sperogenix Therapeutics. For further
information, please visit www.santhera.com.
AGAMREE® is a trademark of Santhera
Pharmaceuticals.
For further information please
contact: public-relations@santhera.com orAndrew Smith,
Chief Financial Officerandrew.smith@santhera.com
About Clinigen Clinigen is a
global, specialist pharmaceutical services company focused on
providing ethical access to medicines. Its mission is to accelerate
access to medicines for patients in every corner of the globe. The
Group supports pharmaceutical and biotech companies across the
medical product lifecycle, from clinical through to commercial and
operates from sites in North America, Europe, Africa and the Asia
Pacific. Clinigen has more than 1,100 employees across five
continents in 15 countries and provides access in more than 130
countries every year. For more information on Clinigen, please
visit http://www.clinigen.com.
Disclaimer / Forward-looking
This communication does not constitute an offer or invitation to
subscribe for or purchase any securities of Santhera
Pharmaceuticals Holding AG. This publication may contain certain
forward-looking statements concerning the Company and its business.
Such statements involve certain risks, uncertainties and other
factors which could cause the actual results, financial condition,
performance or achievements of the Company to be materially
different from those expressed or implied by such statements.
Readers should therefore not place undue reliance on these
statements, particularly not in connection with any contract or
investment decision. The Company disclaims any obligation to update
these forward-looking statements.
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