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Additionally, as indicated in previous filings, there can be no assurance that the results from the Sulonex Phase 3 study will track the data from the pilot Collaborative Study Group Phase 2 study or the DiNAS Phase 2 study. Results from these earlier Sulonex studies may not be indicative of results from future clinical trials and the risk remains that the pivotal program for Sulonex may generate efficacy data that will be insufficient for the approval of the drug, or may raise safety concerns that may prevent approval of the drug.
Some of the statements included in this press release anticipating
future clinical and business prospects for our lead drug candidate Sulonex,
may be forward-looking statements that involve a number of risks and
uncertainties. For those statements, we claim the protection of the safe
harbor for forward- looking statements contained in the Private Securities
Litigation Reform Act of 1995. Among the factors that could cause our
actual results to differ materially are the following: if, upon final
analysis, it is determined that all trials of Sulonex should be terminated,
our ability to successfully adjust our strategy and reduce our operating
expenses in order to properly support the trials of our other drug
candidates; if, upon final analysis of the Phase 3 data, it is determined
that dosing should continue in the Phase 4 study, our ability to complete
enrollment into the Phase 4 study on the timetable previously set for
completion of Phase 4; our ability to complete cost- effective clinical
trials or meet anticipated development timelines for the o
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| SOURCE Keryx Biopharmaceuticals, Inc. Copyright©2008 PR Newswire. All rights reserved |