EyeGate Receives Additional Milestone Payment From Valeant Pharmaceuticals for EGP-437
10 3월 2016 - 9:46AM
Eyegate Pharmaceuticals, Inc. (NASDAQ:EYEG) (“EyeGate” or the
“Company”), a specialty pharmaceutical company that focuses on
developing and commercializing therapeutics and drug delivery
systems for treating diseases of the eye, today announced that it
has received an additional development milestone from Valeant
Pharmaceuticals Luxembourg S.à.r.l. (“Valeant”) under the Company’s
License Agreement with Valeant for the development and
commercialization of the Company’s EGP-437 combination product in
the field of uveitis.
The Company is eligible to receive milestone
payments totaling up to $32.5 million upon and subject to the
achievement of certain specified developmental and commercial
milestones.
Stephen From, President and Chief Executive Officer
of EyeGate Pharmaceuticals commented, “I am pleased with the
progress we have made in our collaboration with Valeant. This
milestone payment is a reflection of the continued advancement of
EyeGate’s drug development initiatives and further demonstrates the
utility of our lead candidate, EGP-437 combination product, in
anterior uveitis.”
About EyeGate:EyeGate is a
clinical-stage specialty pharmaceutical company that is focused on
developing and commercializing therapeutics and drug delivery
systems for treating diseases of the eye. EGP-437, the Company’s
first and only product in clinical trials, incorporates a
reformulated topically active corticosteroid, Dexamethasone
Phosphate that is delivered into the ocular tissues through
EyeGate’s proprietary innovative drug delivery system, the
EyeGate(R) II Delivery System. For more information, please visit
www.EyeGatePharma.com.
Safe Harbor Statement:Some of the
statements in this press release are “forward-looking” and are made
pursuant to the safe harbor provision of the Private Securities
Litigation Reform Act of 1995. These “forward-looking” statements
include statements relating to, among other things, the
commercialization efforts and other regulatory or marketing
approval efforts pertaining to EyeGate’s products, including its
EGP-437 combination product, as well as the success thereof, with
such approvals or success may not be obtained or achieved on a
timely basis or at all. These statements involve risks and
uncertainties that may cause results to differ materially from the
statements set forth in this press release, including, among other
things, certain risk factors described under the heading “Risk
Factors” contained in our Annual Report on Form 10-K filed with the
SEC on March 31, 2015, or described in our other public filings.
Our results may also be affected by factors of which we are not
currently aware. The forward-looking statements in this press
release speak only as of the date of this press release. EyeGate
expressly disclaims any obligation or undertaking to release
publicly any updates or revisions to such statements to reflect any
change in its expectations with regard thereto or any changes in
the events, conditions or circumstances on which any such statement
is based.
Contact:
Lee Roth / Joseph Green
The Ruth Group for Eyegate Pharmaceuticals
646-536-7012 / 7013
lroth@theruthgroup.com / jgreen@theruthgroup.com
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