THE WOODLANDS, Texas--(BUSINESS WIRE)--
Opexa Therapeutics, Inc. (NASDAQ: OPXA), a company developing
personalized immunotherapies for autoimmune disorders, including
multiple sclerosis (MS) and neuromyelitis optica (NMO), today announced
that it has set 5:00 p.m. Eastern Time on March 13, 2022 as the record
date for its upcoming rights offering. Opexa intends to issue
subscription rights to purchase units, composed of a share of Opexa
common stock and a warrant to purchase an additional share of common
stock, to holders of Opexa’s common stock and Series L warrants on the
record date. The subscription rights will expire if they are not
exercised by 5:00 p.m. Eastern Time on April 8, 2015. Opexa may, in its
sole discretion, extend the rights offering for additional periods and
may cancel the rights offering at any time or for any reason prior to
the expiration date. Once made, all exercises of subscription rights are
irrevocable.
Under the rights offering, Opexa will distribute one non-transferable
subscription right for each share of common stock held on the record
date. Opexa’s common stock will trade ex-rights on March 11, 2022. Each
right will entitle the holder to purchase one unit, composed of one
share of common stock and a warrant to purchase common stock at the
subscription price of $0.70 per unit. The three-year warrant will
entitle the holder to purchase one share of common stock at an exercise
price of (i) $0.50 per share from the date of issuance through June 30,
2016, and (ii) $1.50 per share from July 1, 2022 through the warrant
expiration date. Opexa has applied to list the warrants on NASDAQ,
although there is no assurance that a sufficient number of subscription
rights will be exercised so that the warrants will meet the minimum
listing criteria to be accepted for listing on NASDAQ. The warrants will
be redeemable if Opexa’s common stock closes above $2.50 per share for
10 consecutive trading days.
Opexa will also distribute the non-transferable subscription rights to
holders of its Series L warrants who are entitled to participate in the
rights offering pursuant to the terms of the warrants held by them. Each
such Series L warrant holder will receive one subscription right for
each share of common stock into which the Series L warrants are
exercisable as of the record date.
Holders who fully exercise their basic subscription rights will be
entitled, if available, to subscribe for an additional amount of units
that are not purchased by other shareholders or holders of Series L
warrants, on a pro rata basis and subject to ownership limitations.
Opexa plans to use the proceeds from the rights offering primarily to
complete funding for the ongoing Phase IIb “Abili T” clinical study of
Tcelna in patients with secondary progressive multiple sclerosis (SPMS)
through completion and data release, expected in the second half of 2016.
In addition, Opexa plans to continue preclinical and manufacturing
activities for OPX-212 in development for patients with neuromyelitis
optica (NMO), and if such activities are successful, to file an
investigational new drug application with the U.S. Food and Drug
Administration to initiate a Phase 1/2 proof-of-concept study. The
financing will also provide for other general corporate purposes
(including working capital, research and development, business
development and operational purposes).
As soon as practicable following the record date, Opexa intends to mail
to shareholders of record and Series L warrant holders on the record
date a prospectus and related documents for use in exercising
subscription rights. Opexa has engaged Maxim Group LLC as lead
dealer-manager and National Securities Corporation as co-dealer-manager
for the rights offering. Questions about the rights offering or requests
for copies of the prospectus, when available, may be directed to
Advantage Proxy, Inc., the Company's information agent for the rights
offering, by calling (877) 870-8565 (toll-free) or emailing ksmith@advantageproxy.com;
or Maxim Group LLC 405 Lexington Avenue, New York, NY 10174, Attention
Syndicate Department, email syndicate@maximgrp.com
or telephone (212) 895-3745; or National Securities Corporation,
410 Park Avenue, 14th Floor, New York, NY 10022,
Attention Syndicate Department, email kaddarich@nationalsecurities.com
or telephone (212) 417-8164.
The rights offering will be made only by means of a prospectus filed
with the Securities and Exchange Commission as part of the registration
statement relating to the rights offering, which registration statement
was declared effective on February 25, 2022. This press release
does not constitute an offer to sell or the solicitation of an offer to
buy these securities, nor will there be any sale of these securities in
any state or other jurisdiction in which such offer, solicitation or
sale would be unlawful prior to registration or qualification under the
securities laws of any such state or jurisdiction.
About Opexa
Opexa is a biopharmaceutical company developing a personalized
immunotherapy with the potential to treat major illnesses, including
multiple sclerosis (MS) as well as other autoimmune diseases such as
neuromyelitis optica (NMO). These therapies are based on Opexa’s
proprietary T-cell technology. The Company’s leading therapy candidate,
Tcelna®, is a personalized T-cell immunotherapy that is in a Phase IIb
clinical development program (the Abili-T trial) for the treatment of
Secondary Progressive MS. Tcelna is derived from T-cells isolated from
the patient’s peripheral blood, expanded ex vivo, and reintroduced into
the patients via subcutaneous injections. This process triggers a potent
immune response against specific subsets of autoreactive T-cells known
to attack myelin.
For more information, visit the Opexa Therapeutics website at www.opexatherapeutics.com.
Cautionary Statement Relating to Forward - Looking Information for
the Purpose of "Safe Harbor" Provisions of the Private Securities
Litigation Reform Act of 1995
This release contains forward-looking statements which are made
pursuant to the safe harbor provisions of Section 27A of the Securities
Act of 1933, as amended, and Section 21E of the Securities Exchange Act
of 1934, as amended. Statements contained in this release, other than
statements of historical fact, constitute “forward-looking statements.”
The words “expects,” “believes,” “potential,” “possibly,” “estimates,”
“may,” “could” and “intends,” as well as similar expressions, are
intended to identify forward-looking statements. These forward-looking
statements do not constitute guarantees of future performance. Investors
are cautioned that statements which are not strictly historical
statements, including, without limitation, statements regarding plans
and objectives for product development (including for Tcelna
(imilecleucel T) and OPX-212), constitute forward-looking statements.
Such forward-looking statements are subject to a number of risks and
uncertainties that could cause actual results to differ materially from
those anticipated. These risks and uncertainties include, without
limitation, risks associated with the following: market conditions; our
capital position; our ability to compete with larger, better financed
pharmaceutical and biotechnology companies; new approaches to the
treatment of our targeted diseases such as MS and NMO; our expectation
of incurring continued losses; our uncertainty of developing a
marketable product; our ability to raise additional capital to continue
our development programs (including to undertake and complete any
ongoing or further clinical studies for Tcelna, to complete preclinical
development activities and potentially file an IND for OPX-212, and
potentially to conduct a Phase 1/2 proof-of-concept study for OPX-212 in
NMO); our ability to maintain compliance with NASDAQ listing standards;
the success of our clinical trials (including the Phase IIb trial for
Tcelna in secondary progressive MS which, depending upon results, may
determine whether Ares Trading SA (Merck), a wholly owned subsidiary of
Merck Serono S.A., elects to exercise its option (Option) to acquire an
exclusive, worldwide (excluding Japan) license of our Tcelna program for
the treatment of MS); the success of our development programs (including
the preclinical development activities with respect to OPX-212); whether
Merck exercises its Option and, if so, whether we receive any
development or commercialization milestone payments or royalties from
Merck pursuant to the Option; our dependence (if Merck exercises its
Option) on the resources and abilities of Merck for the further
development of Tcelna; the efficacy of Tcelna for any particular
indication, such as for Relapsing Remitting MS or Secondary Progressive
MS; our ability to develop and commercialize products; our ability to
obtain required regulatory approvals; our compliance with all FDA
regulations; our ability to obtain, maintain and protect intellectual
property rights (including for Tcelna and future pipeline candidates
such as OPX-212); the risk of litigation regarding our intellectual
property rights or the rights of third parties; our limited
manufacturing capabilities; our dependence on third-party suppliers and
manufacturers; our ability to hire and retain skilled personnel; our
volatile stock price; and other risks detailed in our filings with the
SEC. These forward-looking statements speak only as of the date made. We
assume no obligation or undertaking to update or revise any
forward-looking statements contained herein to reflect any changes in
our expectations with regard thereto or any change in events, conditions
or circumstances on which any such statement is based. You should,
however, review additional disclosures we make in our registration
statement on Form S-1 for the rights offering that has been declared
effective by the SEC, as well as our Annual Reports on Form 10-K,
Quarterly Reports on Form 10-Q and Current Reports on Form 8-K.
Source: Opexa Therapeutics, Inc.