Solid Biosciences Announces Licensing Agreement with Armatus Bio for the Use of AAV-SLB101, a Proprietary, Muscle-Targeted Capsid, in the Development of an RNAi Therapy to treat FSHD
07 Marzo 2024 - 1:00PM
Solid Biosciences Inc. (Nasdaq: SLDB), a life sciences company
developing precision genetic medicines for neuromuscular and
cardiac diseases, today announced a non-exclusive worldwide license
and collaboration agreement with Armatus Bio for the use of Solid’s
proprietary capsid AAV-SLB101 for the development and
commercialization of Armatus’ vectorized RNAi candidate to treat
Facioscapulohumeral muscular dystrophy (FSHD). The AAV-SLB101
capsid has been shown in preclinical studies to have enhanced
biodistribution and improved expression in muscle cells.
Under the terms of the agreement, Solid granted Armatus a
non-exclusive worldwide license to utilize AAV-SLB101 for treatment
of FSHD and will provide Armatus AAV-SLB101 plasmid material,
preclinical data characterizing AAV-SLB101, and manufacturing and
regulatory know-how to enable development. In return, Solid will
receive an upfront payment, payments upon the achievement of
certain development and sales milestones, and tiered royalties on
net sales for any products incorporating AAV-SLB101. Armatus will
be responsible for the development and commercialization of
licensed products incorporating AAV-SLB101.
“Our transaction with Armatus Bio is the first of what we intend
to be a broad out-licensing of our capsid library to both companies
and academic institutions. We designed AAV-SLB101 for enhanced
biodistribution to skeletal muscle, which is intended to help
improve the efficacy and reduce the toxicity of AAV-delivered gene
therapies for muscular disorders,” said Bo Cumbo, President and
Chief Executive Officer at Solid Biosciences. “AAV-SLB101 is the
capsid for our next-generation Duchenne candidate, SGT-003, and we
are excited to expand AAV-SLB101’s use to FSHD through this
agreement with Armatus Bio.”
Armatus is developing ARM-201, a potential best-in-class, single
dose therapeutic used for the treatment of FSHD, a progressive
genetic neuromuscular disorder caused by DUX4 overexpression.
ARM-201’s proprietary miRNA payload seeks to reduce DUX4, and thus
arrest muscle weakening and atrophy, prevent further degeneration,
and ameliorate the amount of inflammation and oxidative stress
caused by FSHD.
“The use of Solid’s unique AAV-SLB101 capsid will help enable
optimal patient dosing for our FSHD program. The preclinical data
presented to date for AAV-SLB101 demonstrate increased muscle
transduction while simultaneously reducing biodistribution in the
liver. These data, combined with the data we have generated for
ARM-201 give us high confidence in the potential to reduce total
AAV dose levels compared to first generation capsids,” commented
Brian Price, Ph.D., Chief Technology Officer at Armatus Bio.
“Further, we are encouraged by the strong safety profile
demonstrated by AAV-SLB101, which has a cleared IND as the capsid
in Solid’s SGT-003 construct for the treatment of DMD. With this
license in place, we are eager to advance our optimized ARM-201
construct as the lead candidate toward clinical evaluation.”
About AAV-SLB101AAV-SLB101 is a proprietary,
rationally designed capsid developed for enhanced muscle tropism
and reduced liver uptake. With a robust preclinical package in mice
and nonhuman primates, AAV-SLB101 has demonstrated increased
transduction speed, enhanced skeletal and cardiac muscle tropism,
decreased liver biodistribution and improved efficiency when
compared to first generation capsids. The incorporation of
AAV-SLB101 into AAV delivered therapies has the potential to be a
step forward in the treatment of neuromuscular and cardiac
diseases. Solid Biosciences aims to license AAV-SLB101 broadly to
both companies and academic institutions pursuing treatments for
rare diseases.
About Solid BiosciencesSolid Biosciences is a
life sciences company focused on advancing a portfolio of gene
therapy candidates for neuromuscular and cardiac programs,
including SGT-003, for the treatment of Duchenne muscular dystrophy
(Duchenne), SGT-501 for the treatment of catecholaminergic
polymorphic ventricular tachycardia (CPVT), AVB-401 for the
treatment of BAG3-mediated dilated cardiomyopathy, AVB-202-TT for
the treatment of Friedreich’s ataxia, and additional assets for the
treatment of fatal cardiac diseases. Solid is advancing its diverse
pipeline across rare neuromuscular and cardiac diseases, bringing
together experts in science, technology, disease management, and
care. Patient-focused and founded by those directly impacted,
Solid’s mandate is to improve the daily lives of patients living
with these devastating diseases. For more information, please visit
www.solidbio.com.
About Armatus BioArmatus Bio is a privately
held late preclinical stage biotechnology innovator leveraging
vectorized RNAi to address urgent unmet medical needs in
genetically-driven neurological diseases. Based in Columbus, Ohio,
the company is led by a seasoned team with expertise in drug
development and delivery, and partnered with world renowned experts
in vector biology, genomics, and neurology.
Solid Biosciences Forward-Looking
StatementsThis press release contains “forward-looking
statements” within the meaning of the Private Securities Litigation
Reform Act of 1995, including statements regarding future
expectations, plans and prospects for the company; the ability to
successfully achieve and execute on the company’s priorities and
achieve key clinical milestones; the company’s SGT-003 program,
including expectations for initiating dosing; potential milestone
payments or royalty payments in connection with the collaboration;
the potential benefits of the collaboration; the safety or
potential efficacy of AAV-SLB101; Solid’s plans to broadly license
AAV-SLB101 and its capsid library to both companies and academic
institutions; and other statements containing the words
“anticipate,” “believe,” “continue,” “could,” “estimate,” “expect,”
“intend,” “may,” “plan,” “potential,” “predict,” “project,”
“should,” “target,” “would,” “working” and similar expressions. Any
forward-looking statements are based on management’s current
expectations of future events and are subject to a number of risks
and uncertainties that could cause actual results to differ
materially and adversely from those set forth in, or implied by,
such forward-looking statements. These risks and uncertainties
include, but are not limited to, risks associated with each party’s
ability to perform its obligations under the collaboration; the
ability to recognize the anticipated benefits of Solid’s
acquisition of AavantiBio; the company’s ability to advance
SGT-003, SGT-501, AVB-401, AVB-202-TT and other preclinical
programs and capsid libraries on the timelines expected or at all;
obtain and maintain necessary approvals from the FDA and other
regulatory authorities; replicate in clinical trials positive
results found in preclinical studies of the company’s product
candidates; obtain, maintain or protect intellectual property
rights related to its product candidates; compete successfully with
other companies that are seeking to develop Duchenne and other
neuromuscular and cardiac treatments and gene therapies; manage
expenses; and raise the substantial additional capital needed, on
the timeline necessary, to continue development of SGT-003,
SGT-501, AVB-401, AVB-202-TT and other candidates, achieve its
other business objectives and continue as a going concern. For a
discussion of other risks and uncertainties, and other important
factors, any of which could cause the company’s actual results to
differ from those contained in the forward-looking statements, see
the “Risk Factors” section, as well as discussions of potential
risks, uncertainties and other important factors, in the company’s
most recent filings with the Securities and Exchange Commission. In
addition, the forward-looking statements included in this press
release represent the company’s views as of the date hereof and
should not be relied upon as representing the company’s views as of
any date subsequent to the date hereof. The company anticipates
that subsequent events and developments will cause the company's
views to change. However, while the company may elect to update
these forward-looking statements at some point in the future, the
company specifically disclaims any obligation to do so.
Solid Biosciences Contact:Leah MonteiroVP, Investor Relations
and Communications617-766-3430lmonteiro@solidbio.com
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