Scottsdale, Arizona 10/30/2008 1:30:39 AM
News / Finance

Oxygen Biotherapeutics Inc. (OXBO.OB) to Submit Test Protocol to FDA for Multi-Center Study for Traumatic Brain Injury

www.QualityStocks.Net would like to highlight Oxygen Biotherapeutics Inc. (OTCBB: OXBO). The Company is dedicated to commercializing innovative pharmaceuticals and medical devices in the field of oxygen therapeutics and continuous substrate monitoring. The Company has under development a perfluorocarbon therapeutic oxygen carrier and liquid ventilation product and an implantable glucose sensor. These products are based upon core technologies that include biomedical applications for PFCs and medical and industrial applications for biosensors.

 

In the company’s news yesterday,

 

Oxygen Biotherapeutics Inc. announced it will submit an amended test protocol to the U.S. Food and Drug Administration, as well as in Canada, to cover the dose escalation studies of the company’s therapeutic oxygen carrier Oxycyte. The company plans on recruiting 40 traumatic brain injury (TBI) patients in each country to test the safety and efficacy of Oxycyte.

 

“Personally, I think that the extensive data we will collect in the dose escalation studies should be more than needed for proof-of-concept in both safety and efficacy. The advantage is that we should have the data we need much earlier, after each cohort of 10, rather than after 200 patients as it was previously planned. Another important advantage is that this approach could save us a substantial amount of money – perhaps as much as 50 percent compared to the original phase IIb design. Most importantly, having good data sooner could give us a much earlier opportunity to reach out to potential license partners,” said company chairman and CEO Chris J. Stern, DBA.

 

Oxygen Biotherapeutics’ multi-center studies will seek to determine the lowest dose of Oxycyte that reduces thrombocytopenia while providing clinical benefit in TBI. After receiving the assigned dose level, each patient will be followed and observed for six months.

 

Oxygen Biotherapeutics will file the amendment in a global format, allowing the company to submit the protocol in the United States, as well as abroad, within about 50 days. Patient enrollment is scheduled for the first quarter of 2009; and the company is negotiating whether or not to conduct an additional study in Switzerland.

 

The company will finance the escalation study partially with a previously-announced $1.9 million grant from the United States Department of Defense to M. Ross Bullock, M.D., Ph.D., of the University Of Miami Miller School Of Medicine, Department of Neurosurgery. According to the press release, Dr. Bullock is the principal investigator for the traumatic brain injury trial protocol with Oxycyte.

 

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Forward-Looking Statement:

This release may contain forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. All forward-looking statements are inherently uncertain as they are based on current expectations and assumptions concerning future events or future performance of the company. Readers are cautioned not to place undue reliance on these forward-looking statements, which are only predictions and speak only as of the date hereof. Risks and uncertainties applicable to the company and its business could cause the company's actual results to differ materially from those indicated in any forward-looking statements.