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Generex Announces Enrollment of Over 150 Patients in Phase III Trial of Generex Oral-lyn WORCESTER, Mass., Aug. 12, 2008 (PRIME NEWSWIRE) -- Generex
Biotechnology Corporation (NasdaqCM:GNBT - News) (http://www.generex.com),
the leader in drug delivery for metabolic diseases through
the inner lining of the mouth, announced today that it has
enrolled over 150 patients in the Company's pivotal Phase
III clinical trial of Generex Oral-lyn(tm), its flagship
proprietary oral insulin spray product. Of those patients,
over 100 have been dosed. There are 55 sites in the United
States, Canada, Bulgaria, Russia, Poland and Ukraine actively
screening and enrolling patients, including 39 clinical
trial sites where patients are being dosed. Generex Oral-lyn(tm)
has been shipped to all of the sites. ``We are pleased to report that the enrollment and dosing of additional patients into the trial is progressing,'' said George Markus, the Company's Vice President of Regulatory and Scientific Affairs. ``We continue to look forward to dosing initiation in more patients and are encouraged by the continuity and progress of this pivotal study.'' The Phase III study will involve up to 750 patients with Type-1 Diabetes Mellitus within centers in the United States, Canada, EU, Russia, Poland, Bulgaria, Romania and Ukraine. The objective of the six-month study is to compare the efficacy of Generex Oral-lyn and the Company's RapidMist(tm) Diabetes Management System with prandial injections of regular human insulin as measured by HbA1c. The Company believes that Generex Oral-lyn will offer a safe, simple, fast, effective, and pain-free alternative to prandial insulin injections, which will improve patient compliance with therapeutic regimes, thereby delaying the progress of diabetes and the onset of its myriad complications. Generex Oral-lyn is presently approved for commercial sale in India and Ecuador. The delivery of Generex Oral-lyn clinical supplies to global sites and centers, including Ukraine and Russia, is ongoing with other regional rollout to follow. About Generex Biotechnology Corporation Generex is engaged in the research, development, and commercialization of drug delivery systems and technologies. Generex has developed a proprietary platform technology for the delivery of drugs into the human body through the oral cavity (with no deposit in the lungs). The Company's proprietary liquid formulations allow drugs typically administered by injection to be absorbed into the body by the lining of the inner mouth using the Company's proprietary RapidMist(tm) device. The Company's flagship product, oral insulin (Generex Oral-lyn(tm)), which is available for sale in Ecuador for the treatment of patients with Type-1 and Type-2 diabetes and which was approved for sale in India in October 2007, is in Phase 3 clinical trials at several sites around the world. For more information, visit the Generex website at http://www.generex.com. The Generex Biotechnology Corp. logo is available at http://www.primenewswire.com/newsroom/prs/?pkgid=3831 Safe Harbor Statement This release and oral statements made from time to time by Generex representatives concerning the same subject matter may contain ``forward-looking statements'' within the meaning of the Private Securities Litigation Reform Act of 1995. These statements can be identified by introductory words such as ``expects,'' ``plans,'' ``intends,'' ``believes,'' ``will,'' ``estimates,'' ``forecasts,'' ``projects'' or words of similar meaning, and by the fact that they do not relate strictly to historical or current facts. Forward-looking statements frequently are used in discussing potential product applications, potential collaborations, product development activities, clinical studies, regulatory submissions and approvals, and similar operating matters. Many factors may cause actual results to differ from forward-looking statements, including inaccurate assumptions and a broad variety of risks and uncertainties, some of which are known and others of which are not. Known risks and uncertainties include those identified from time to time in the reports filed by Generex with the Securities and Exchange Commission, which should be considered together with any forward-looking statement. No forward-looking statement is a guarantee of future results or events, and one should avoid placing undue reliance on such statements. Generex undertakes no obligation to update publicly any forward-looking statements, whether as a result of new information, future events or otherwise. Generex cannot be sure when or if it will be permitted by regulatory agencies to undertake additional clinical trials or to commence any particular phase of clinical trials. Because of this, statements regarding the expected timing of clinical trials cannot be regarded as actual predictions of when Generex will obtain regulatory approval for any ``phase'' of clinical trials. Generex claims the protection of the safe harbor for forward-looking statements that is contained in the Private Securities Litigation Reform Act. Contact: CEOcast, Inc.
Gary Nash
212-732-4300
American Capital Ventures, Inc.
For Generex:
Howard Gostfrand
877-918-0774
Source: Generex Biotechnology Corp.
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