SIGA Technologies, Inc. (NASDAQ: SIGA), a commercial-stage
pharmaceutical company focused on health security and infectious
disease, announced today that it entered into an amendment to its
international promotion agreement with Meridian Medical
Technologies, Inc. (Meridian). Effective June 1, SIGA will drive
international promotion activities for oral TPOXX® while
maintaining its contractual relationship with Meridian to maintain
continuity for key customer relationships.
“We are excited about the long-term growth opportunities for
oral TPOXX and believe this amendment to the Meridian promotion
agreement will be instrumental in driving our expansion efforts for
TPOXX outside the U.S.,” said Diem Nguyen, Chief Executive Officer.
“This strategic move, which gives SIGA greater control, will enable
us to meet our global customers’ needs more effectively during
these uncertain times of orthopox threats. The ability to forge
direct relationships with key international stakeholders is
essential to our plans to expand access to TPOXX and maximize value
creation.”
This amendment, which extends the term of the promotion
agreement by two years with respect to specific territories
including the European Union, gives SIGA primary responsibility for
promoting oral TPOXX. Certain existing contracts under the
promotion agreement, including Meridian’s contract with the
European Commission’s DG Health Emergency Preparedness and
Response Authority (HERA), will remain in effect.
ABOUT SIGA TECHNOLOGIES, INC. SIGA
Technologies, Inc. is a commercial-stage pharmaceutical
company focused on the health security market. Health security
comprises countermeasures for biological, chemical, radiological
and nuclear attacks (biodefense market), vaccines and therapies for
emerging infectious diseases, and health preparedness. Our lead
product is TPOXX®, also known as tecovirimat and ST-246®, an orally
administered and IV formulation antiviral drug for the treatment of
human smallpox disease caused by variola virus.
ABOUT TPOXX® TPOXX is a novel
small-molecule drug and the U.S. maintains a supply of TPOXX under
Project BioShield. The oral formulation of TPOXX was approved by
the FDA for the treatment of smallpox in 2018, and the IV
formulation was approved for the same indication in 2022. The full
label is available by clicking here. Oral
tecovirimat received approval from the European Medicines
Agency (EMA) and the Medicines and Healthcare Products
Regulatory Agency (MHRA) in the United Kingdom in
2022. The EMA and UK approvals include labeling for oral
tecovirimat indicating its use for the treatment of smallpox,
monkeypox, cowpox, and vaccinia complications following vaccination
against smallpox. The full label is available
by clicking here. In September 2018,
SIGA signed a contract with the Biomedical Advanced Research
and Development Authority (BARDA), part of the office of the
Administration for Strategic Preparedness and Response within
the U.S. Department of Health and Human Services, for
additional procurement and development related to both oral and
intravenous formulations of TPOXX. For more information about SIGA,
please visit www.siga.com.
ABOUT ORTHOPOXVIRUSESOrthopoxvirus, belonging
to the family of poxvirus that infect humans, include smallpox,
mpox, cowpox and vaccinia. Smallpox, a highly contagious and fatal
disease, presents itself as a risk to global health security today
given fears of its release accidentally or intentionally as a
bioweapon. Mpox virus, similar to smallpox, causes
intermittent human infections, painful lesions, and possible case
fatalities. Mpox outbreaks have been observed recently in the
US, Europe, and Central & West Africa. Whether
through natural occurrence or potential bioweapon warfare, orthopox
threatens global health. Anti-virals and vaccines serve as possible
solutions to address these threats.
FORWARD-LOOKING STATEMENTSThis press release
contains “forward-looking statements” within the meaning of the
Private Securities Litigation Reform Act of 1995, as amended,
including statements relating to SIGA’s future business development
including securing new contracts and partnerships. The words or
phrases “can be,” “expects,” “may affect,” “may depend,”
“believes,” “estimate,” “project” and similar words and phrases are
intended to identify such forward-looking statements. Such
forward-looking statements are subject to various known and unknown
risks and uncertainties, and SIGA cautions you that any
forward-looking information provided by or on behalf of
SIGA is not a guarantee of future performance. SIGA’s actual
results could differ materially from those anticipated by such
forward-looking statements due to a number of factors, some of
which are beyond SIGA’s control, including, but not limited to, (i)
the risk that BARDA elects, in its sole discretion as permitted
under the 19C BARDA Contract (the “BARDA Contract”), not to
exercise all, or any, of the remaining unexercised options under
those contracts, (ii) the risk that SIGA may not complete
performance under the BARDA Contract on schedule or in
accordance with contractual terms, (iii) the risk that the BARDA
Contract, U.S. Department of Defense contracts are
modified or canceled at the request or requirement of the U.S.
Government, (iv) the risk that the nascent international biodefense
market does not develop to a degree that allows SIGA to continue to
successfully market TPOXX internationally, (v) the risk that
potential products, including potential alternative uses or
formulations of TPOXX that appear promising to SIGA or its
collaborators, cannot be shown to be efficacious or safe in
subsequent pre-clinical or clinical trials, (vi) the risk that
target timing for deliveries of product to customers, and the
recognition of related revenues, are delayed or adversely impacted
by the actions, or inaction, of contract manufacturing
organizations, or other vendors, within the supply chain, or due to
coordination activities between the customer and supply chain
vendors, (vii) the risk that SIGA or its collaborators will not
obtain appropriate or necessary governmental approvals to market
these or other potential products or uses, (viii) the risk that
SIGA may not be able to secure or enforce sufficient legal rights
in its products, including intellectual property protection, (ix)
the risk that any challenge to SIGA’s patent and other property
rights, if adversely determined, could affect SIGA’s business and,
even if determined favorably, could be costly, (x) the risk that
regulatory requirements applicable to SIGA’s products may result in
the need for further or additional testing or documentation that
will delay or prevent SIGA from seeking or obtaining needed
approvals to market these products, (xi) the risk that the volatile
and competitive nature of the biotechnology industry may hamper
SIGA’s efforts to develop or market its products, (xii) the risk
that changes in domestic or foreign economic and market conditions
may affect SIGA’s ability to advance its research or may affect its
products adversely, (xiii) the effect of federal, state, and
foreign regulation, including drug regulation and international
trade regulation, on SIGA’s businesses, (xiv) the risk of
disruptions to SIGA’s supply chain for the manufacture of
TPOXX®, causing delays in SIGA’s research and development
activities, causing delays or the re-allocation of funding in
connection with SIGA’s government contracts, or diverting the
attention of government staff overseeing SIGA’s government
contracts, (xv) risks associated with actions or
uncertainties surrounding the debt ceiling, (xvi) the risk
that the U.S. or foreign governments' responses
(including inaction) to national or global economic conditions or
infectious diseases, such as COVID-19, are ineffective and may
adversely affect SIGA’s business, and (xvii) risks associated with
responding to the current mpox outbreak, as well as the risks and
uncertainties included in Item 1A “Risk Factors” of our Annual
Report on Form 10-K for the year ended December 31,
2023 and SIGA's subsequent filings with the Securities
and Exchange Commission. SIGA urges investors and security holders
to read those documents free of charge at
the SEC's website
at http://www.sec.gov. All such
forward-looking statements are current only as of the date on which
such statements were made. SIGA does not undertake any obligation
to update publicly any forward-looking statement to reflect events
or circumstances after the date on which any such statement is made
or to reflect the occurrence of unanticipated events.
The information contained in this press release does not
necessarily reflect the position or the policy of the Government
and no official endorsement should be inferred.
Contacts:
InvestorsLaine Yonker, Edison
Grouplyonker@edisongroup.com |
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MediaHolly Stevens, Berry &
Companyhstevens@berrypr.com |
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