EyeGate Announces $3.77 Million Registered Direct Offering
2016年6月27日 - 9:00PM
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 entered into a definitive agreement with a single healthcare
dedicated institutional investor to purchase shares of common stock
and shares of Series A Convertible Preferred Stock for
aggregate gross proceeds of approximately $3.77 million in a
registered direct offering.
The Company agreed to sell an aggregate of 441,000
shares of common stock at a price of $2.25 per share and 2,776.5
shares of Series A Convertible Preferred Stock, at a price of
$1,000 per share. The Series A Convertible Preferred Stock is
convertible at any time into an aggregate of approximately 1.23
million shares of common stock at an initial conversion price of
$2.25 per share, subject to certain ownership limitations. The
Series A Convertible Preferred Stock is only entitled to dividends
in the event dividends are paid on the Company's common stock and
will not have any preferences over the Company's common stock, with
the exception of a $0.01 per share liquidation preference.
Additionally, the investor will receive, for each share of common
stock or for each share of common stock issuable upon conversion of
a share of Series A Preferred Stock purchased in the registered
direct offering, a warrant to purchase one-half of a share of
common stock at an exercise price of $3.50 per share. The
warrant issued to the investor shall be initially exercisable six
months following issuance and terminate five years following the
initial exercise date. The closing of the offering is
expected to take place on or about June 30, 2016, subject to the
satisfaction of customary closing conditions.
Rodman & Renshaw, a unit of H.C. Wainwright
& Co., LLC, acted as the exclusive placement agent in
connection with this offering.
EyeGate intends to use the net proceeds to obtain
additional capital to support its operations, including for
clinical trials, for working capital and for other general
corporate purposes, which will include the pursuit of other
research and development efforts and could also include the
acquisition or in-license of other products, product candidates or
technologies, though no such acquisition or in-license is current
contemplated. EyeGate has not yet determined the amount of
net proceeds to be used specifically for any of the foregoing
purposes.
The shares of common stock and Series A Convertible
Preferred Stock (including the shares of common stock issuable upon
conversion of the Series A Convertible Preferred Stock) described
above (but not the warrants or the shares of common stock
underlying the warrants) will be offered and sold by EyeGate
pursuant to an effective shelf registration statement on
Form S-3, which was filed with the Securities and Exchange
Commission (the “SEC”) on April 1, 2016 and subsequently declared
effective on May 6, 2016 (File No. 333-210557) (the
“Registration Statement”), and the base prospectus dated as of May
6, 2016 contained therein. EyeGate will file a prospectus
supplement with the SEC in connection with the sale of the shares
of its common stock and Series A Convertible Preferred Stock.
Copies of the prospectus supplement, together with the accompanying
prospectus, when available, can be obtained at the SEC's website at
http://www.sec.gov, by request at H.C. Wainwright & Co.,
430 Park Avenue, New York, NY, 10022 by e-mailing
placements@hcwco.com.
The warrants and the shares of common stock
underlying the warrants to be issued in the offering have not been
registered under the Securities Act of 1933, as amended (the
“Securities Act”), or applicable state securities laws.
Accordingly, the warrants and underlying shares of common stock
underlying the warrants may not be offered or sold in the United
States except pursuant to an effective registration statement or an
applicable exemption from the registration requirements of the
Securities Act and such applicable state securities laws.
This press release shall not constitute an offer to
sell or the solicitation of an offer to buy any of the securities
described herein. There shall not be any offer, solicitation of an
offer to buy, or sale of securities in any state or jurisdiction in
which such an offering, solicitation, or sale would be unlawful
prior to registration or qualification under the securities laws of
any such state or jurisdiction.
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® II Delivery System. In addition,
EyeGate is developing, through its wholly-owned Jade subsidiary,
products using cross-linked thiolated carboxymethyl hyaluronic acid
(“CMHA-S”), a modified form of the natural polymer hyaluronic acid
(HA), which possesses unique physical and chemical properties such
as viscoelasticity and water retention. The ability of CMHA-S to
adhere longer to the ocular surface, resist degradation and protect
the ocular surface makes it well-suited for treating various ocular
surface injuries. EyeGate intends to initiate a clinical study for
Jade’s lead product candidate for corneal epithelial defects. 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, EyeGate’s expectations regarding the
completion, timing, pricing and size of the offering described in
this press release, whether expressed or implied, the
commercialization efforts and other regulatory or marketing
approval efforts pertaining to EyeGate’s products, including
EyeGate’s EGP-437 combination product, and those of Jade
Therapeutics, Inc., a wholly owned subsidiary of EyeGate, 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 EyeGate’s Annual Report on
Form 10-K filed with the SEC on March 30, 2016, EyeGate’s Quarterly
Report on Form 10-Q filed with the SEC on May 13, 2016 or described
in EyeGate’s other public filings. EyeGate’s results may also be
affected by factors of which EyeGate is 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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