GSK’s candidate Shingles Vaccine Containing Agenus’ QS-21 Stimulon® Demonstrates 90% Efficacy against Shingles an...
October 27 2015 - 6:55AM
Business Wire
Agenus Inc. (NASDAQ:AGEN), an immunology company discovering and
developing innovative treatments for cancer and other diseases,
announced today that GlaxoSmithKline’s plc
(LSE/NYSE:GSK) second pivotal Phase III efficacy study
of its shingles vaccine candidate containing
Agenus’ QS-21 Stimulon® adjuvant
demonstrated 90% overall efficacy against shingles
compared to placebo. In this trial known as ZOE-70
(Zoster efficacy in adults aged 70 years and over) the
vaccine candidate HZ/su was studied in
adults aged 70 years and older.i These results
are consistent with the first pivotal Phase III
study, ZOE-50, which demonstrated an efficacy
of 97.2% in adults age 50 years and
older. In ZOE-50, 53% of the subjects were over 60, and almost
24% were over 70 years of age.ii
“We are pleased by the consistent, positive
results from studies of the candidate vaccine
containing our
adjuvant, QS-21 Stimulon,” said Dr. Garo Armen,
Ph.D., Chairman and Chief Executive Officer of Agenus. “We
look forward to worldwide regulatory filings of
HZ/su for the many millions of people,
especially older individuals, at risk of shingles.”
The HZ/su vaccine candidate combines the glycoprotein E
(gE) from the chickenpox virus, Varicella, a protein that is part
of the virus that causes shingles, with the AS01 adjuvant
system, which is designed to enhance the immune
response to gE. The AS01 adjuvant system contains Agenus’ QS-21
Stimulon, MPL (3-O-desacyl-4’-monophosphoryl lipid A) and
liposomes. GSK intends to submit a regulatory application to
the US Food and Drug Administration (FDA), and regulatory agencies
in Japan and EU for HZ/su in mid-2016.
About ZOE-70
The ZOE-70 HZ/su shingles study is a randomized,
observer-blind, placebo controlled Phase III trial involving
approximately 14,800 adults. The
vaccine candidate is also being evaluated in immune
compromised patient populations in other clinical trials.
About Shingles
Shingles typically presents as a painful, itchy rash that
develops in a circumscribed region of the body, as a result of
reactivation of latent chickenpox virus (varicella zoster virus,
VZV). Complications from shingles can include post-herpetic
neuralgia (PHN), a condition of chronic
neuropathic pain, as well as scarring, vision
complications, secondary infection, and nerve palsies. A person’s
risk for shingles increases after 50 years of age. The
individual lifetime risk of developing shingles is approximately
one in three people; however, for individuals who reach the
age of 85, this risk increases to one in two people.iii
About AgenusAgenus is an immunology company engaged in
the discovery and development of immuno-therapies,
including novel checkpoint modulators, vaccines and adjuvants
to treat cancer and other diseases. Using its proprietary platforms
Retrocyte Display™ and SECANT®, the Company is discovering and
developing novel antibodies to target GITR, OX40, CTLA-4, LAG-3,
TIM-3, PD-1, CEACAM1 and other undisclosed checkpoints in partnered
and internal programs. The Company’s QS-21 Stimulon®
adjuvant is partnered with GlaxoSmithKline and Janssen
Sciences Ireland UC. Agenus’ heat shock protein vaccine,
Prophage™, has successfully completed Phase 2 studies in newly
diagnosed glioblastoma multiforme. For more information,
please visit www.agenusbio.com; information that may be important
to investors will be routinely posted on our website.
Forward-Looking StatementsThis 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 benefits
of GSK’s HZ/su vaccine candidate. 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 Agenus’ Form 10-Q filed with the Securities and
Exchange Commission on August 3, 2015. 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.
i https://clinicaltrials.gov/ct2/show/NCT01165229?term=zoster+022&rank=1
ii Lal H, Cunningham AL, Godeaux
O, Chlibek R, Diez-Domingo J, Hwang SJ, Levin MJ,
McElhaney
JE, Poder A, Puig-Barberà J, Vesikari T,
Watanabe D, Weckx L, Zahaf T, Heineman TC; ZOE-50 Study
Group. Efficacy of an adjuvanted herpes zoster
subunit vaccine in older adults. N Engl J Med. 2015;
372(22):2087-96
iii S. Pinchinat et al.: Similar herpes zoster
incidence across Europe: results from a systematic literature
review. BMC Infectious Diseases 2013,
13:170
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version on businesswire.com: http://www.businesswire.com/news/home/20151027005877/en/
Agenus Inc.Michelle Linn,
774-696-3803michelle.linn@agenusbio.comorMedia:BMC
CommunicationsBrad Miles,
646-513-3125bmiles@bmccommunications.comorInvestors:Argot
PartnersAndrea Rabney, 212-600-1902andrea@argotpartners.comorJamie
Maarten, 212-600-1902jamie@argotpartners.com
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