timates," or variations of such words are intended to identify such
forward-looking statements. All statements in this release regarding the
future outlook related to Duska are forward-looking statements, including
the statements that Duska's ATPace entering a pivotal Phase 3 clinical
trial, Duska's CDP-1050 commencing a Phase 2 clinical trial, the belief
that the initial dose of ATPace will be significantly more efficacious than
the initial labeled dose of adenosine in terminating PSVT, the belief that
ATP has dual inhibitory action, the anticipated launch of the key product
and the potential future growth of Duska, the submission of a revised
protocol to the FDA for Special Protocol Assessment procedure approval, the
initiation of a single, prospective, double-blind, placebo- controlled and
randomized trial in patients presenting to the emergency room with PSVT to
demonstrate ATPace's clinical safety and efficacy, the filing of a New Drug
Application under section 505(b)(2) and the development of new chemical
entities to target a newly discovered pathway in the pathophysiology of
chronic obstructive pulmonary disease. The forward-looking statements are
subject to risks and uncertainties that could cause actual results to
differ materially from those set forth or implied by any forward-looking
statements. Such risks include the risk that the clinical trial for
approval of ATPace and the Phase 2 clinical trial for our CDP-1050 may not
be successful, the ability of DSM to meet our specifications and timeline
as well as the FDA requirements of a commercial drug manufacturer and that
our technology may not lead to expected results including the development
or the successful commercialization of technologies relating to the use of
ATP. Additional uncertainties and risks are described in Duska's most
recently filed SEC documents, such as its most recent annual report on Form
10-KSB, all quarterly reports on Form 10-QSB and any current reports on
Form 8-K filed since the
'/>"/>SOURCE Duska Therapeutics, Inc. Copyright©2008 PR Newswire. All rights reserved | |
Page: 1 2 3 4 5 Related medicine news :1.
Duska Therapeutics Acquires Technology for ATPotent Sperm Motility Program2.
Duska Therapeutics Receives Comments From FDA on Phase 3 ATPace(TM) Protocol Synopsis3.
Duska Therapeutics Sponsored University of Pennsylvania Study Demonstrates ATP Improves Sperm Motility and In Vitro Fertilization in Animals4.
Duska Therapeutics Plans 505(b)(2) NDA Filing Route for ATPace(TM)5.
Transition Therapeutics to Hold Conference Call on First Quarter Fiscal 2009 Financial Results on Monday, November 10th, at 4:30 P.M. EST6.
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Cell Therapeutics, Inc. (CTI) Oppenheimer & Co. Healthcare Conference Presentation to be Webcast