Full Press Release Details
Publishes Study Showing GSK's Shingles Vaccine Containing Agenus' QS-21
Stimulon Adjuvant Provides over 97% Protection in People Over the Age
simultaneously presented at ECCMID
vaccine achieves nearly 98% protection in people 70 or older
marks the second successful Phase 3 clinical program incorporating
Agenus' QS-21 Stimulon adjuvant
LEXINGTON, Mass.--(BUSINESS WIRE)--April 28, 2015--Agenus Inc. (NASDAQ:
AGEN), an immunology company developing innovative treatments for
cancers and other diseases, announced today that primary and secondary
endpoint data from GlaxoSmithKline's (LSE/NYSE: GSK) randomized Phase 3
trial of HZ/su, a vaccine candidate for the prevention of shingles, was
simultaneously presented at the 25th Scientific Conference of the
European Society of Clinical Microbiology and Infectious Disease
(ECCMID) in Copenhagen, and published in the New England Journal of
Medicine. GSK's HZ/su incorporates Agenus' QS-21 Stimulon adjuvant,
which is designed to increase immune response to antigens.
The data show that GSK's HZ/su reduced the risk of shingles (herpes
zoster) by 97.2% in adults aged 50 and older, compared to placebo.
Importantly, the protection was maintained across all studied age
groups, ranging from 96.6% in subjects aged 50-59, 97.4% in those aged
60-69, and 97.9% in those aged 70 or older. No major safety concerns
were identified in the study. The most common reported adverse event was
pain at injection site, fatigue and myalgia.
"The vast majority of adults over age 50 are at high risk of
reactivating the varicella zoster virus, which leads to shingles and its
painful and debilitating symptoms. These clinical results point to the
broad benefits that widespread use of this vaccine could bring to adults
over 50 worldwide," said Garo Armen, Ph.D., Chairman and CEO of Agenus.
"These data, and those from GSK's RTS,S malaria vaccine now undergoing
regulatory review by the EMA, highlight the importance and value that we
believe QS-21 Stimulon brings to vaccines and to Agenus."
The HZ/su vaccine candidate combines gE, a protein that is part of the
virus that causes shingles, with the AS01 adjuvant system, which
enhances the immune response to gE. The AS01 adjuvant system contains
Agenus' QS-21 Stimulon, MPL (3-O-desacyl-4'-monophosphoryl lipid A) and
Agenus is eligible to receive a milestone payment upon GSK's first
approval of a QS-21 Stimulon-containing product and royalties from any
potential commercial product sales of HZ/su. QS-21 Stimulon is being
evaluated in more than 12 additional vaccine candidates.
The HZ/su shingles study is a randomized, observer-blind,
placebo-controlled Phase 3 trial involving over 16,000 adults aged 50
years and older. The study started in August 2010 and is still ongoing.
In addition to older adults, HZ/su is being evaluated in
immunocompromised patient populations, including solid and hematological
cancer patients, hematopoietic stem cell and renal transplant recipients
and HIV-infected people.
Shingles typically presents as a painful, itchy rash that develops on
one side of the body, as a result of reactivation of latent chickenpox
virus (varicella zoster virus, VZV). Complications from shingles can
include chronic pain, scarring, vision complications, secondary
infection, nerve palsies and hospitalization. A person's risk for
shingles increases sharply after 50 years of age. The individual
lifetime risk of developing shingles is approximately one in three
people; however, for individuals aged 85 and over, this risk increases
to one in two people.i
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.
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
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 therapeutic benefit of
GSK's singles vaccine candidate HZ/su in adults over the age of 50
worldwide, potential commercial sales of HZ/su and the potential for
Agenus to receive milestone and royalty payments for product candidates
containing Agenus' QS-21 Stimulon generally. These forward-looking