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Bone Bank Allografts Becomes First Tissue Bank to Select the Recently-Launched Clearant Sterilization Service.


LOS ANGELES -- Clearant, Inc. (OTCBB OTCBB

See OTC Bulletin Board (OTCBB).
: CLRI CLRI Central Leather Research Institute (India) ), the developer of the patent-protected CLEARANT PROCESS(R) for pathogen inactivation inactivation /in·ac·ti·va·tion/ (in-ak?ti-va´shun) the destruction of biological activity, as of a virus, by the action of heat or other agent. , announced today that Bone Bank Allografts allografts (al´graf´ts),
n.pl the transplantation of tissue between genetically nonidentical individuals of the same species.
, a leading tissue bank, has become the first company to select the Clearant Sterilization sterilization

Any surgical procedure intended to end fertility permanently (see contraception). Such operations remove or interrupt the anatomical pathways through which the cells involved in fertilization travel (see reproductive system).
 Service for its tissue sterilization needs. Bone Bank Allografts, which distributes 30,000 allografts annually, will utilize Clearant's Sterilization Service on a variety of human-sourced bone and connective soft-tissue allograft allograft: see transplantation, medical.  implants. The Clearant Sterilization Service, which was launched earlier this month, is a complementary offering to the CLEARANT PROCESS(R) for tissue banks, allowing use of Clearant's technology on a pay-per-order basis.

"Based on my previous experience with utilizing the CLEARANT PROCESS(R), I am confident Bone Bank Allografts' clients will benefit from the higher sterility assurance levels associated with this special tissue sterilization process," said John Lee, COO of Bone Bank Allografts. "Clearant's innovative business model for access to this technology makes the tissue sterilization process more streamlined, and more practical to apply."

In order to use the new Clearant Sterilization Service, a client tissue bank will soak the tissue in a radioprotectant solution developed by Clearant. The tissue bank then transfers the tissue to Clearant's Chicago-area facility where it will be sterilized ster·il·ize  
tr.v. ster·il·ized, ster·il·iz·ing, ster·il·iz·es
1. To make free from live bacteria or other microorganisms.

2.
 using controlled levels of radiation. The terminally-sealed and sterilized tissue may be returned to the tissue bank within 72 hours. No long-term contract is necessary for clients to access this service.

"The favorable response we have received from tissue banks at the recent American Association of Tissue Banks Conference has quickly turned into an agreement," said Alain Delongchamp, Chief Executive Officer of Clearant, Inc. "Clearant offers the only commercially-available technology that meets final-packaging sterility levels equal to those of medical devices while maintaining tissue integrity. Results to date, combined with the recent FDA FDA
abbr.
Food and Drug Administration


FDA,
n.pr See Food and Drug Administration.

FDA,
n.pr the abbreviation for the Food and Drug Administration.
 guidance on Good Tissue Practices, should increasingly drive tissue banks to employ our technology."

In addition to Bone Bank Allografts' announced agreement to adopt the Clearant Sterilization Service, Clearant holds five North American North American

named after North America.


North American blastomycosis
see North American blastomycosis.

North American cattle tick
see boophilusannulatus.
 tissue license agreements for the CLEARANT PROCESS(R).

About Clearant, Inc.

Clearant, Inc., a biotechnology company headquartered in Los Angeles, California, is a leader in pathogen inactivation for biological products. Clearant, Inc. has developed the patent-protected CLEARANT PROCESS(R), designed to substantially reduce all types of pathogens in biological products while maintaining a high degree of the underlying protein. Various sterilization methods on the market today only kill specific types of pathogens, such as bacteria or lipid-enveloped viruses, for specific products. The CLEARANT PROCESS(R) can substantially reduce all types of pathogens for products across many market segments including plasma proteins, tissue implants, recombinant products and blood products, and can be applied at various stages of product processing/manufacturing, including in the final container.

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 Safe Harbor

1. A legal provision to reduce or eliminate liability as long as good faith is demonstrated.

2. A form of shark repellent implemented by a target company acquiring a business that is so poorly regulated that the target itself is less attractive.
 provisions of the Private Securities Litigation Reform Act The Private Securities Litigation Reform Act of 1995 (PSLRA) implemented several significant substantive changes affecting certain cases brought under the federal securities laws, including changes related to pleading, discovery, liability, class representation and awards fees and  of 1995. 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, intense competition and substantial regulation in the biotechnology industry, and additional risks discussed in the company's filings with the SEC.

For more information about Clearant, Inc., please see www.clearant.com.
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No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2005, Gale Group. All rights reserved. Gale Group is a Thomson Corporation Company.

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Publication:Business Wire
Geographic Code:1USA
Date:Sep 27, 2005
Words:567
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