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Contact:
GTx, Inc.
Carney Duntsch
Investor and Media Relations
901-523-9700 ext. 170 cduntsch@gtxinc.com |
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Burns McClellan, Inc.
Jonathan M. Nugent (investors)
Kathy L. Jones-Nugent, Ph.D. (media)
212-213-0006 |
GTx,
Inc. to Webcast Analyst Meeting Wednesday, September 29, 2004
MEMPHIS, Tenn., Sept. 22 /PRNewswire-FirstCall/
-- GTx, Inc. (Nasdaq: GTXI) today announced that it will host a live
webcast of its analyst briefing at 4:30 p.m. Eastern Time on Wednesday,
September 29, 2004. During the meeting, members of the Company's senior
management will discuss the Company's product pipeline and provide
an in-depth discussion of the Company's technology and commercialization
strategy.
Mitchell Steiner, M.D., F.A.C.S., Vice-Chairman and
Chief Executive Officer of GTx will be joined by Marc Hanover, President
and Chief Operating Officer. Special guest speakers will include
Peter Scardino, M.D., F.A.C.S., Chairman of the Department of Urology
at Memorial Sloan Kettering; Samir Taneja, M.D., Associate Professor
of Urology at New York University; Paul Sieber, M.D., Urological
Associates of Lancaster, Ltd.; and Bill Evans, Ph.D., Geriatrics,
Physiology, and Nutrition at the University of Arkansas.
To access the live webcast, visit the Investor Relations
section of the GTx website at http://www.gtxinc.com. A replay of
the webcast will be available online until October 13, 2004.
About GTx
GTx is a biopharmaceutical company dedicated to the discovery, development
and commercialization of therapeutics primarily related to the treatment
of serious men's health conditions. GTx's drug discovery and development
programs are focused on small molecules that selectively modulate
the effects of estrogens and androgens. GTx currently has two product
candidates that are in human clinical trials. The company is developing
ACAPODENE™, its most advanced product candidate, through clinical
trials for two separate indications: (1) its now completed Phase
IIb clinical trial for the reduction in the incidence of prostate
cancer in high risk men with precancerous prostate lesions and planned
initiation of a Phase III clinical trial (2) a pivotal Phase III
clinical trial for the treatment of serious side effects of advanced
prostate cancer therapy. GTx is developing its second product candidate,
andarine, and other specified backup compounds, with its partner,
Ortho Biotech Products, L.P., a subsidiary of Johnson & Johnson.
It is currently anticipated that andarine will be entering a planned
Phase II clinical trial later this year. GTx retains all rights
to the discovery, development, and commercialization of the rest
of its SARM program including its other specific product candidates
ostarine, prostarine and andromustine.
Forward Looking Statement
This press release contains forward-looking statements, including,
without limitation, statements related to GTx's current and anticipated
clinical trials and research and development programs. These forward-looking
statements are based upon GTx's current expectations. Forward-looking
statements involve risks and uncertainties. GTx's actual results
and the timing of events could differ materially from those anticipated
in such forward-looking statements as a result of these risks and
uncertainties, which include, without limitation, risks that neither
GTx nor its partner will be able to commercialize its product candidates
if preclinical studies do not produce successful results or clinical
trials do not demonstrate safety and efficacy in humans; if third
parties do not manufacture the Company's product candidates in sufficient
quantities and at an acceptable cost, clinical development and commercialization
of its product candidates would be delayed; use of third-party manufacturers
may increase the risk that the Company will not have adequate supplies
of its product candidates; if third parties on whom the Company
relies do not perform as contractually required or expected, the
Company may not be able to obtain regulatory approval for or commercialize
its product candidates; the Company is dependent upon collaborative
arrangements to complete the development and commercialization of
some of its product candidates, and these collaborative arrangements
may place the development of its product candidates outside its
control, may require it to relinquish important rights or may otherwise
be on terms unfavorable to the Company; and if the Company is not
able to obtain required regulatory approvals, the Company will not
be able to commercialize its product candidates. The annual report
filed on Form 10-K with the U.S. Securities and Exchange Commission
on March 26, 2004 contains under the heading "Additional Factors
That Might Affect Future Results" a more comprehensive description
of these and other risks to which GTx is subject. GTx expressly
disclaims any obligation or undertaking to release publicly any
updates or revisions to any forward-looking statements contained
herein to reflect any change in its expectations with regard thereto
or any change in events, conditions or circumstances on which any
such statements are based.
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