DALLAS, Feb. 22 /PRNewswire-FirstCall/ -- HemoBioTech announced today that Dr. Arthur P. Bollon, Chairman and CEO of HemoBioTech will make a presentation at the MedTech Insight conference “Investment in Innovation (In3)West: a Preview of Early-Stage Medical Technology companies” in Irvine, California on February 23, 2006.
The conference features several emerging medical technology companies and will be attended by investment bankers, venture capitalists and company executives.
About HemoBioTech, Inc.
HemoBioTech is engaged in the development of HemoTech(TM), a novel human blood substitute technology exclusively licensed from Texas Tech University Health Science Center. HemoTech(TM) is chemically modified hemoglobin, which not only carries oxygen in the blood, but can also induce red blood cell production. The Company believes that HemoTech(TM) may possess properties that diminish the intrinsic toxicities which have plagued other attempts at developing blood substitutes, based upon pre-clinical and initial human clinical trials undertaken outside the U.S. by prior holders of this technology. HemoTech(TM) is being developed to help reduce or eliminate the danger resulting from acute blood loss in trauma, as well as for other conditions. Corporate headquarters are located at J. P. Morgan International Plaza, 14221 Dallas Parkway, Suite 1400, Dallas, Texas 75254. For further information contact Dr. Arthur Bollon at 214-540-8411 or arthurb@flash.net . The Company website is http://www.hemobiotech.com .
Safe Harbor Statement
Except for historical information, the matters discussed in this news release may be considered “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. Such statements include declarations regarding the intent, belief or current expectations of HemoBioTech and its management and are valid only as of today, and we disclaim any obligation to update this information. These statements are subject to known and unknown risks and uncertainties that may cause actual future experience and results to differ materially from the statements made. Factors that might cause such a difference include, among others the successful pre- clinical development, the successful completion of clinical trials, the FDA review process and other governmental regulation, pharmaceutical collaborator interest and ability to successfully develop and commercialize drug candidates, competition from other pharmaceutical companies, product pricing and third party reimbursement, and other factors which are included in HemoBioTech’s prospectus dated May 13, 2005, as supplemented, and HemoBioTech’s other reports filed with the Securities and Exchange Commission.
HemoBioTech, Inc.
CONTACT: Dr. Arthur Bollon of HemoBioTech, Inc., +1-214-540-8411, orarthurb@flash.net
Web site: http://www.hemobiotech.com/
