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CYTOMEDIX AUTOLOGEL™ CLINICAL TRIAL PRESENTATION RECEIVES TOP AWARD AT APMA ANNUAL MEETING

ROCKVILLE, Md., Aug 23, 2006 – Cytomedix, Inc. (AMEX: GTF), today announced that a presentation based on the clinical trial for the AutoloGel™ System, received the “Outstanding Oral Abstract Presentation” award at the American Podiatric Medical Association Annual Scientific Meeting that was held August 7 though 10 in Las Vegas, NV.

The award-winning presentation was based on the abstract “A Prospective, Randomized, Controlled, Blinded, Multicenter Pivotal Trial of a Platelet-Rich Plasma Gel Versus Control When Added to the Standard of Care in the Treatment of Non-Healing Diabetic Foot Ulcers,” and was delivered by Vickie R. Driver, DPM, MS, Director of Clinical Research at the Center for Lower Extremity Ambulatory Research (CLEAR) at the Dr. William M Scholl College of Podiatric Medicine at Rosalind Franklin University of Medicine and Science in North Chicago, and Chief of the National Center for Limb Preservation at Advocate Lutheran General Hospital in Park Ridge Illinois. Dr. Driver was an investigator in the AutoloGel™ clinical trial. This data was also published recently in the peer-reviewed journal, Ostomy/Wound Management.

Dr. Driver commented, “I am honored and pleased to receive such a distinguished award from my colleagues at APMA. It is with sincere gratitude that I congratulate Cytomedix for developing this new novel therapy to help treat diabetic foot ulcers. When these new therapies are developed, it is, without question, vital that we spend the money and conduct clinical research trials to better understand how patients will benefit. We need to continue to support biomedical companies that support pivotal research to help us heal diabetic foot wounds and thereby prevent or reduce amputations.”

“We are extremely pleased that this presentation by Dr. Driver should receive such a prestigious award at the annual meeting of the country’s leading podiatric medical professionals,” stated Chairman and Chief Executive Officer Kshitij Mohan. “This is further evidence that the medical profession has begun to see the merits of the AutoloGel™ System for use on chronic foot ulcers in people with diabetes. Cytomedix congratulates Dr. Driver for her outstanding performance and is honored and grateful for her research on the AutoloGel™ System.”

The APMA Annual Meeting was attended by approximately 4,000 medical lower extremity specialists who witnessed hundreds of presentations and speeches in the course of the four-day Annual Scientific Meeting.

ABOUT THE AMERICAN PODIATRIC MEDICAL ASSOCIATION

The American Podiatric Medical Association is the premier professional organization representing the nation's Doctors of Podiatric Medicine (podiatrists). The APMA represents approximately 80 percent of the podiatrists in the country. Within APMA's umbrella of organizations are 53 component societies in states and other jurisdictions, as well as 21 affiliated and related societies.

APMA's Council on Podiatric Medical Education is the body designated by the US Department of Education to accredit the nation's podiatric medical schools. In addition, the Council has the responsibility to approve residency programs and continuing medical education programs. The Council recognizes certifying boards within podiatric medicine which meet its standards.


ABOUT CYTOMEDIX

Cytomedix, Inc. is a biotechnology company specializing in processes and products derived from autologous platelet releasates for uses with wounds and other applications. The current offering is AutoloGel™System, a process that utilizes an autologous platelet gel composed of multiple growth factors, other platelet releasates, and fibrin matrix. The Company has announced favorable results from its blinded, prospective, multi-center clinical trial on the use of its technology with diabetic foot ulcers. Additional information regarding Cytomedix is available at: http://www.cytomedix.com

SAFE HARBOR STATEMENT

Statements contained in this press release not relating to historical facts are forward-looking statements that are intended to fall within the safe harbor rule for such statements under the Private Securities Litigation Reform Act of 1995. The information contained in the forward-looking statements is inherently uncertain, and Cytomedix's actual results may differ materially due to a number of factors, many of which are beyond Cytomedix's ability to predict or control, including among others, the success of new sales initiatives, governmental regulation, acceptance by the medical community and competition. There is no guarantee that the FDA will complete its review of the Company’s 510(k) submission for a specific wound healing indication within any estimated timeframe, or that the FDA will fully agree with the Company in the interpretation of the data or the regulatory pathway and provide marketing clearance. Further, even assuming the FDA grants the Company’s request for marketing clearance, there is no guarantee that the Company will receive Medicare reimbursement for its product; the Company’s marketing efforts will be successful; or that it will be able to achieve its other strategic goals.

There is no guarantee that the information reported by Dr. Driver in the presentation discussed above is accurate or that further review of Dr. Driver’s’ conclusions or testing of AutoloGel ™ will prove such information to be accurate. There is also no guarantee that the Company’s current capitalization will be sufficient to attain its goals or that future funding will be available to the Company on acceptable terms. These forward-looking statements are subject to known and unknown risks and uncertainties that could cause actual events to differ from the forward-looking statements. More information about some of these risks and uncertainties may be found in the reports filed with the Securities and Exchange Commission by Cytomedix, Inc. Except as is expressly required by the federal securities laws, Cytomedix undertakes no obligation to update or revise any forward-looking statements, whether as a result of new information, changed circumstances or future events or for any other reason.


SOURCE: Cytomedix, Inc.

The Wall Street Group, Inc.
Ron Stabiner
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