stock & financial message boards
  Login  |  Register |  Site Map  |  Blogs |  Recent Activity  |  Members  | Glossary
Ticker/Industry
  Joined Today: 0

« Previous | Next » | All Messages |  CLRI Message Board Home | recommend post |  Ignore Poster

Message #29
From: Stock News Bot
Date: November 6, 2006 05:00:00 AM

CLRI News Clearant Announces Record Direct Distribution of Sterile Implants in October

LOS ANGELES--(BUSINESS WIRE)--Clearant, Inc. (OTCBB:CLRI) today announced that 26 Clearant Process® Sterile Implant cervical spinal and soft tissue allograft implants were distributed directly during the month of October. This is a significant increase, as direct distribution of implants has grown 50 percent from the monthly average in the third quarter, which was the company’s first full quarter under the new growth initiative.

Launched in the last few days of June, Clearant’s direct distribution, which makes Clearant Process® Sterile Implants directly available to surgeons and clinics, has resulted in continued growth. In addition to the 26 implants distributed directly by Clearant to the orthopedic surgeon community, an estimated 400 to 500 additional implants were distributed by Clearant licensees during the month of October.

“We are highly encouraged by the past month’s results, demonstrating the growing demand for sterilized implants by surgeons,” said Clearant Chief Executive Officer Alain Delongchamp. “We anticipate that the demand for sterile implants will continue to grow as we reach out to more surgeons and continue to expand the number of Clearant Process® product offerings.”

Clearant’s implants are sterilized using the Clearant Process®, a sterilization technology that virtually eliminates the risk of infection in bone and soft-tissue allograft implants while preserving their functional viability.

About Clearant, Inc.

Clearant, Inc. is a leader in pathogen inactivation for biological products. Clearant has developed the patent-protected Clearant Process, which substantially reduces all types of bacteria and viruses in biological products while maintaining the functionality of the underlying tissue implant or protein. The Company began to distribute directly to surgeons, hospitals and clinics Clearant Process sterile implants in June 2006; in addition, Clearant continues to license the Clearant Process and provides its patented sterilization services to tissue banks and other biological products manufacturers. As of the end of 1Q 2006, Clearant had 10 license and service agreements with tissue banks. To date more than 9,000 patients have been successfully implanted with Clearant Process sterile implants supplied by one of the Company's licensed partners. Whereas various competing sterilization methods only kill specific types of pathogens (such as bacteria or lipid-enveloped viruses) for specific products, the Clearant Process reduces all types of pathogens for products across many market segments including tissue implants, plasma proteins, recombinant products, medical devices and blood products. Also, the Clearant Process can be applied at various stages of product processing and/or manufacturing, including in the final packaging. For more information, please visit www.clearant.com.

Forward-Looking Statements

Except for statements of historical fact, the matters discussed in this press release are forward looking and made pursuant to the Safe Harbor provisions of the Private Securities Litigation Reform Act of 1995, in particular statements regarding surgeons strongly recommending the use of implants with tissue treated by the CLEARANT PROCESS, and the conclusions from a study by surgeons to build demand for sterilized tissue. These forward-looking statements reflect numerous assumptions and involve a variety of risks and uncertainties, many of which are beyond the company's control, which may cause actual results to differ materially from stated expectations. These risk factors include, among others, limited operating history, difficulty in developing, exploiting and protecting proprietary technologies, results of additional clinical studies, acceptance and success of our direct distribution of allografts, efficacy of the technology, intense competition and substantial regulation in the biotechnology industry, and additional risks discussed in the company's filings with the SEC, available on the SEC web site http://www.sec.gov.

« Previous | Next » | All Messages |  CLRI Message Board Home | Ignore Poster