UNITED
STATES
SECURITIES
AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM
8-K
CURRENT REPORT
Pursuant
to Section 13 or 15(d) of The Securities Exchange Act of 1934
Date
of Report (Date of earliest event reported): April 24, 2015
AGENUS INC.
(Exact
name of registrant as specified in its charter)
DELAWARE
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000-29089
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06-1562417
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(State or other jurisdiction
of incorporation)
|
(Commission
File Number)
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(IRS Employer
Identification No.)
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3 Forbes Road
Lexington, MA
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02421
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(Address of principal executive offices)
|
(Zip
Code)
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Registrant’s
telephone number, including area code 781-674-4400
N/A
(Former
name or former address, if changed since last report.)
Check the appropriate box below if the Form 8-K filing is intended to
simultaneously satisfy the filing obligation of the registrant under any
of the following provisions (see General Instruction A.2. below):
⃞
Written
communications pursuant to Rule 425 under the Securities Act (17 CFR
230.425)
⃞
Soliciting
material pursuant to Rule 14a-12 under the Exchange Act (17 CFR
240.14a-12)
⃞
Pre-commencement
communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR
240.14d-2(b))
⃞
Pre-commencement
communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR
240.13e-4(c))
Item 8.01 Other Events.
On April 24, 2015, Agenus Inc. issued a press release titled, “GSK’s
Malaria Vaccine Phase 3 Study Containing AGENUS’ QS-21 Published in The
Lancet” (the “Press Release”). A copy of the Press Release is
attached hereto as Exhibit 99.1 and is incorporated herein by reference.
Item 9.01 Financial Statements and Exhibits.
(d) Exhibits
Exhibit No.
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Description of Exhibit
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99.1
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Press Release dated April 24, 2015.
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SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the
registrant has duly caused this report to be signed on its behalf by the
undersigned hereunto duly authorized.
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AGENUS INC.
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Date:
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April 24, 2015
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|
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By:
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/s/ Garo H. Armen
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Garo H. Armen
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Chairman and CEO
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EXHIBIT INDEX
Exhibit No.
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Description of Exhibit
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99.1
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Press Release dated April 24, 2015.
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Exhibit 99.1
GSK’s
Malaria Vaccine Phase 3 Study Containing Agenus’ QS-21 Published in The
Lancet
-
Final
study results show significant reduction in malaria cases
-
EMA
currently reviewing the regulatory application
LEXINGTON, Mass.--(BUSINESS WIRE)--April 24, 2015--Agenus Inc. (NASDAQ:
AGEN), an immunology company developing innovative treatments for
cancers and other diseases, announced today that final results from a
large-scale Phase 3 study of GlaxoSmithKline’s (NYSE: GSK) malaria
vaccine candidate, RTS,S, were published in The Lancet. The
study demonstrated a statistically significant reduction against malaria
in children who received RTS,S followed by a booster shot of the vaccine
at 18 months. RTS,S incorporates QS-21 Stimulon®,
Agenus’ adjuvant designed to increase the immune response to antigens in
vaccines.
The study results also showed:
-
RTS,S reduced the number of cases of clinical malaria in young
children (aged 5-17 months at first vaccination) by 36%, and in
infants (aged 6-12 weeks) by 26% over an average follow-up period of
48 months.
-
This resulted in an average reduction of 1,774 cases of clinical
malaria for every 1,000 children vaccinated (aged 5-17 months), and an
average reduction of 983 cases of clinical malaria for every 1,000
infants vaccinated over an average 36-month follow-up. Children
receiving the vaccine candidate but not a booster dose had lower rates
of protection. The study showed that RTS,S averted even more cases of
malaria in areas with higher transmission rates.
“We’re proud to be a part of this malaria vaccine initiative, which has
the potential to save tens of thousands of lives each year,” said Garo
Armen, Ph.D., Chairman and CEO of Agenus. “These compelling results
demonstrate for the first time that a vaccine and adjuvant can
significantly reduce suffering by young children in areas hardest hit by
malaria. We look forward to RTS,S potentially achieving regulatory
approval and being made available to the millions of children who are at
risk of severe malaria in sub-Saharan African countries.”
Agenus is eligible for a milestone payment upon approval of RTS,S and
royalties from potential commercial sales. QS-21 Stimulon is being
evaluated in more than 12 additional vaccine candidates.
RTS,S trial data were submitted to the European Medicines Agency (EMA)
in June 2014 for review by their Committee for Medicinal Products for
Human Use (CHMP). A positive opinion from the CHMP, together with a
potential policy recommendation from the World Health Organization
(anticipated by the end of 2015), would be the basis for licensure
applications to the National Regulatory Authorities (NRAs) in
sub-Saharan African countries.
Eleven research centers in seven African countries conducted the trial,
in partnership with GSK and the Path Malaria Vaccine Initiative (MVI),
with grant funding from the Bill & Melinda Gates Foundation to MVI. The
trial, launched in 2009 and concluded in January 2014, enrolled 15,459
young child (5-17 months) and infant (6-12 weeks) participants.
About QS-21 Stimulon®
QS-21 Stimulon is a
saponin extracted from the bark of the Quillaja saponaria tree,
an evergreen also known as the soap bark tree. The adjuvant is a key
component of investigational vaccines to prevent a wide variety of
infectious diseases, and therapeutic vaccines for cancer and
degenerative disorders. QS-21 Stimulon has been evaluated in
approximately 50,000 patients. Agenus is generally entitled to receive
milestone payments as QS-21 Stimulon containing programs advance, as
well as royalties on potential commercial sales for 10 years after
commercial launch, if ever, with some exceptions.
About Agenus
Agenus is an immunology company developing a
series of Checkpoint Modulators for the treatment of patients with
cancer, infectious diseases, and other immune disorders, heat shock
protein (HSP)-based vaccines, and immune adjuvants. These programs are
supported by three separate technology platforms. Agenus’ internal and
partnered checkpoint modulator programs target GITR, OX40, CTLA-4,
LAG-3, TIM-3, PD-1 and other undisclosed programs. The company’s
proprietary discovery engine Retrocyte DisplayTM is used to
generate fully human and humanized therapeutic antibody drug candidates.
The Retrocyte Display platform uses a high-throughput approach
incorporating IgG format human antibody libraries expressed in mammalian
B-lineage cells. Agenus recently acquired a powerful yeast antibody
display platform termed SECANT, developed by Celexion, LLC. SECANT
allows rapid generation of soluble, full-length human antibodies. SECANT
and Agenus’ mammalian antibody display platform have complementary
strengths and further bolster Agenus' abilities to generate and optimize
fully human monoclonal antibodies. Agenus’ heat shock protein-based
vaccines have completed Phase 2 studies in newly diagnosed glioblastoma
multiforme, and in the treatment of herpes simplex viral infection; the
heat shock protein-based vaccine platform can generate personalized as
well as off the shelf products. The company’s QS-21 Stimulon® adjuvant
platform is extensively partnered with GlaxoSmithKline and with Janssen
Sciences Ireland UC and includes several candidates in Phase 2 trials,
as well as shingles and malaria vaccines which have successfully
completed Phase 3 clinical trials. For more information, please visit www.agenusbio.com,
or connect with the company on Facebook, LinkedIn, Twitter and Google+;
information that may be important to investors will be routinely posted
in these locations.
Forward-Looking Statement
This press release contains
forward-looking statements that are made pursuant to the safe harbor
provisions of the federal securities laws, including statements
regarding the potential regulatory approval of GSK’s malaria vaccine
candidate, RTS,S, the potential for RTS,S to save lives each year,
potential commercial sales of RTS,S and the potential for Agenus to
receive milestone and royalty payments for product candidates containing
Agenus’s QS-21 Stimulon generally. These forward-looking statements are
subject to risks and uncertainties that could cause actual results to
differ materially. These risks and uncertainties include, among others,
the factors described under the Risk Factors section of our most recent
Quarterly Report on Form 10-Q or annual report on Form 10-K filed with
the Securities and Exchange Commission. Agenus cautions investors not to
place considerable reliance on the forward-looking statements contained
in this release. These statements speak only as of the date of this
press release, and Agenus undertakes no obligation to update or revise
the statements, other than to the extent required by law. All
forward-looking statements are expressly qualified in their entirety by
this cautionary statement.
CONTACT:
For Agenus
Media
BMC Communications
Brad
Miles, 646-513-3125
bmiles@bmccommunications.com
or
Investors
Argot
Partners
Andrea Rabney/Jamie Maarten, 212-600-1902
andrea@argotpartners.com
jamie@argotpartners.com
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