TorreyPines Therapeutics Completes Second Phase I Study for NGX267, a Selective M1 Agonist for the Treatment of Alzheimer's Dis
July 24 2006 - 8:30AM
PR Newswire (US)
SAN DIEGO, July 24 /PRNewswire/ -- TorreyPines Therapeutics, Inc.
today announced completion of its second Phase I study with NGX267
in clinical development for the treatment of Alzheimer's disease.
This study evaluated the safety of NGX267 in healthy elderly
volunteers. In a previous Phase I study, NGX267, administered as
single doses, was shown to be well-tolerated in healthy, younger
adult males. NGX267, a selective cholinergic muscarinic, or M1,
receptor agonist, has demonstrated potential in providing both
symptomatic improvement and disease modification in animal models
of Alzheimer's disease. This second Phase I study was a
double-blind, placebo-controlled, single ascending dose study that
evaluated the safety, tolerability and pharmacokinetics of NGX267
in healthy males and females between the ages of 65 and 80,
reflecting the age of the primary Alzheimer's disease population.
The trial enrolled 26 volunteers at one center in the U.S. Clinical
data showed that NGX267 was well tolerated at single doses up to
and including 15 mg and that evidence of cholinergic activation was
detected at these doses. Additionally, exposure levels of NGX267 in
elderly men and women at doses of 15 mg or lower may be comparable
to those levels tested in a transgenic mouse study, published in
the journal Neuron (Vol 49, 671-682) in March of this year. In that
animal study, NGX267 improved behavioral symptoms and lowered brain
AB42, a toxic peptide that is the major component of amyloid
plaques. These plaques are considered a primary histopathological
hallmark of Alzheimer's disease. "These favorable safety data in a
population at highest risk of developing Alzheimer's disease
support development of NGX267 as a potential therapy for
Alzheimer's disease," said Neil Kurtz, M.D., President and Chief
Executive Officer of TorreyPines. "This compound may potentially
provide patients and caregivers with a meaningful advance in the
treatment of this disease by addressing both the symptoms and the
progression of Alzheimer's disease." About TorreyPines Therapeutics
TorreyPines Therapeutics, Inc. is a biopharmaceutical company that
discovers and develops small molecule drugs to treat diseases and
disorders of the central nervous system. Led by an accomplished
management team, TorreyPines is leveraging novel drug targets and
technologies to deliver new therapies for migraine, chronic pain,
including neuropathic pain, and Alzheimer's disease. Its therapies
are intended to offer advantages over current therapies. On June 8,
2006, TorreyPines announced that it had entered into a definitive
merger agreement with Axonyx Inc. (NASDAQ:AXYX). The resulting
company will be named TorreyPines Therapeutics, Inc. and be
headquartered in San Diego. Further information is available at
http://www.torreypinestherapeutics.com/ . Additional Information
about the Merger and Where to Find It In connection with the
proposed merger, Axonyx and TorreyPines Therapeutics intend to file
relevant materials with the Securities and Exchange Commission
(SEC), including a registration statement on Form S-4 that will
contain a prospectus and a joint proxy statement. Investors and
security holders of Axonyx and TorreyPines Therapeutics are urged
to read these materials when they become available because they
will contain important information about Axonyx, TorreyPines
Therapeutics and the merger. The proxy statement, prospectus and
other relevant materials (when they become available), and any
other documents filed by Axonyx with the SEC, may be obtained free
of charge at the SEC's web site at http://www.sec.gov/. In
addition, investors and security holders may obtain free copies of
the documents filed with the SEC by Axonyx by directing a written
request to: Axonyx, 500 Seventh Avenue, 10th Floor, New York, NY
10018, Attention: Investor Relations. Investors and security
holders are urged to read the proxy statement, prospectus and the
other relevant materials when they become available before making
any voting or investment decision with respect to the merger. This
communication shall not constitute an offer to sell or the
solicitation of an offer to sell or the solicitation of an offer to
buy any securities, nor shall there be any sale of securities in
any jurisdiction in which such offer, solicitation or sale would be
unlawful prior to registration or qualification under the
securities laws of any such jurisdiction. No offering of securities
shall be made except by means of a prospectus meeting the
requirements of Section 10 of the Securities Act of 1933, as
amended. Participants in the Solicitation Axonyx and its directors
and executive officers and TorreyPines Therapeutics and its
directors and executive officers may be deemed to be participants
in the solicitation of proxies from the stockholders of Axonyx in
connection with the proposed transaction. Information regarding the
special interests of these directors and executive officers in the
merger transaction will be included in the proxy
statement/prospectus referred to above. Additional information
regarding the directors and executive officers of Axonyx is also
included in Axonyx's Annual Report on Form 10-K for the year ended
December 31, 2005, which was filed with the SEC on March 16, 2006.
This document is available free of charge at the SEC's web site
(http://www.sec.gov/) and from Investor Relations at Axonyx at the
address described above. This press release contains and the
presentation made at the conference may contain forward-looking
statements or predictions, including statements regarding the
potential closing of the proposed merger between Axonyx and
TorreyPines Therapeutics and the combined company resulting from
the merger. Actual results may differ materially from the above
forward-looking statements due to a number of important factors,
including the possibility that the proposed merger may not
ultimately close for any of a number of reasons, including, but not
limited to, Axonyx not obtaining shareholder approval of the
issuance of shares and warrants in the merger, the change in
control resulting from the merger or the reverse split of Axonyx
common stock; TorreyPines Therapeutics not obtaining shareholder
approval of the merger, the possibility that NASDAQ will not
approve the listing of the combined company's shares for trading on
the NASDAQ Stock Market or that the combined company will not be
able to meet the continued listing requirements after the closing
of the merger; that Axonyx and TorreyPines Therapeutics will forego
business opportunities while the merger is pending; that prior to
the closing of the proposed transaction, the businesses of the
companies, including the retention of key employees, may suffer due
to uncertainty; and even in the event the transaction is completed,
that combining Axonyx and TorreyPines Therapeutics may not result
in a stronger company, that the technologies and clinical programs
of the two companies may not be compatible and that the parties may
be unable to successfully execute their integration strategies or
realize the expected benefits of the merger. Risks and
uncertainties that could materially affect Axonyx are described in
the documents Axonyx files from time to time with the SEC,
including Axonyx's annual report on Form 10-K. Statements with
regard to product candidates of either Axonyx or TorreyPines
Therapeutics are subject to risks and uncertainties relating to
development, regulatory approval and commercialization, including
whether any preclinical studies or clinical trials, either ongoing
or conducted in the future, will prove successful, and if
successful, whether the results can be replicated; whether safety
and efficacy profiles of any of its drug candidates will be
established, or if established, will remain the same, be better or
worse in future clinical trials, if any; whether pre-clinical
results will be substantiated by ongoing or future clinical trials,
if any, or whether any of its drug candidates will be able to
improve the signs or symptoms of their respective clinical
indication; whether any of its drug candidates will support an NDA
filing, will be approved by the FDA or its equivalent, or if
approved, will prove competitive in the market; or whether the
necessary financing to support its drug development programs will
be available. Neither Axonyx nor TorreyPines Therapeutics
undertakes any obligation to publicly release the result of any
revisions to such forward-looking statements that may be made to
reflect events or circumstances after the date hereof or to reflect
the occurrence of unanticipated events. DATASOURCE: TorreyPines
Therapeutics, Inc. CONTACT: Evelyn Graham of TorreyPines
Therapeutics, Inc., +1-858-623-5665, ext. 118, ; or Media, Patricia
Garrison, +1-917-322-2567, , or Investors, Rhonda Chiger,
+1-917-322-2569, , both of Rx Communications, for TorreyPines
Therapeutics, Inc. Web site:
http://www.torreypinestherapeutics.com/
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