are evaluating
our lead MEK inhibitor, RDEA119, in a Phase 1 study in advanced cancer
patients, and have completed a Phase 1 study in normal healthy volunteers
as a precursor to trials in patients with inflammatory diseases. Lastly, we
have evaluated our second-generation MEK inhibitor for the treatment of
cancer and inflammatory diseases, RDEA436, in a human micro-dose
pharmacokinetic study and have selected it for clinical development.
Statements contained in this press release regarding matters that are
not historical facts are "forward-looking statements" within the meaning of
the Private Securities Litigation Reform Act of 1995. Because such
statements are subject to risks and uncertainties, actual results may
differ materially from those expressed or implied by such forward-looking
statements. Such statements include, but are not limited to, statements
regarding our goals, including the expected properties and benefits of
RDEA806, RDEA427, RDEA594, RDEA119, RDEA436 and our other compounds and the
results of preclinical, clinical and other studies. Risks that contribute
to the uncertain nature of the
forward-looking statements include: risks related to the outcome of
preclinical and clinical studies, risks related to regulatory approvals,
delays in commencement of preclinical and clinical studies, and costs
associated with our drug discovery and development programs and business
development activities. These and other risks and uncertainties are
described more fully in our most recently filed SEC documents, including
our Annual Report on Form 10-K and our Quarterly Reports on Form 10-Q,
under the headings "Risk Factors." All forward-looking statements contained
in this press release speak only as of the date on which they were made. We
undertake no obligation to update such statements to reflect events that
occur or circumstances that exist after the date on which they were made.
'/>"/>SOURCE Ardea Biosciences, Inc. Copyright©2008 PR Newswire. All rights reserved | |
Page: 1 2 Related medicine technology :1.
Ardea Biosciences Advances Lead Product Candidate for the Treatment of Gout, RDEA594, Into Phase 1 Clinical Trial2.
Ardea Biosciences Presents Phase 2a Antiviral Activity Data for Lead HIV Candidate, RDEA806 at XVII International AIDS Conference3.
Ardea Biosciences Reports Additional Positive Phase 2a Results for Lead HIV Candidate, RDEA806, Demonstrating Up to 1.9 Log Reduction in Plasma Viral Load with Once-Daily Dosing4.
Ardea Announces Progress with HIV Non-Nucleoside Reverse Transcriptase Inhibitor Program5.
Ardea Biosciences Presents Preclinical Data on RDEA119 Demonstrating Favorable Anti-Inflammatory Profile for Potential Use in Ulcerative Colitis6.
Ardea Biosciences Identifies Lead Development Candidate for Gout, RDEA5947.
Ardea Biosciences Appoints John W. Beck Chief Financial Officer, Announces Clinical Development Progress and Reports First Quarter 2008 Financial Results8.
Ardea Biosciences Presents Data Demonstrating Favorable Pharmacokinetics and Efficacy for Mitogen-Activated ERK Kinase (MEK) Inhibitors9.
Ardea Biosciences Reports Positive Phase 2a Results for Lead HIV Candidate, RDEA806, Demonstrating up to 2.0 Log Reduction in Plasma Viral Load10.
Ardea Biosciences Presents Preclinical Data Demonstrating Favorable Resistance Profiles for Non-Nucleoside Reverse Transcriptase Inhibitors for the Treatment of Human Immunodeficiency Virus11.
Ardea Biosciences, Inc. Announces New Clinical Development Program Directed Toward the Treatment of Gout