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ArTec Inc., of Reno, Nevada, Announces Its Readiness to Review PRECLINICAL APPLICATION with US FDA - Tubercin-Anti-Cancer Immunostimulant.


RENO, Nev. -- ArTec, Inc., www.artec-inc.net (Pink Sheets:ATKJ) The Pharmaceutical Company's Board of Directors has given a directive to management to prepare for PRECLINICAL US 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.
 APPLICATION. Specifically, a committee was designated the responsibility to prepare for reviewing PRIVATE MEDICAL REGULATORY CONSULTANTS to lead ArTec, Inc.'s efforts. In the PRECLINICAL phase: in vitro in vitro /in vi·tro/ (in ve´tro) [L.] within a glass; observable in a test tube; in an artificial environment.

in vi·tro
adj.
In an artificial environment outside a living organism.
 and in vivo in vivo /in vi·vo/ (ve´vo) [L.] within the living body.

in vi·vo
adj.
Within a living organism.



in vivo adv.
, non-human studies are considered. In the same vein, ArTec, Inc., will prepare to review possible PRECLINICAL COLLABORATORS. At the PRECLINICAL stage, determination will be made about the basis for applying under the investigational new drug application (IND) to the FDA.

The stages for PHASE 1, PHASE 2 and PHASE 3 consist of human studies. At the beginning, ArTec, Inc. plans to include resources involving CLINICAL COLLABERATORS, ALLIANCES and possible GRANTS-SPECIAL RESEARCH PROJECTS to assist Tubercin in completing the FDA approval process. No doubt the FAST TRACK status will also be considered in light of the origin of Tubercin at a highly accredited accredited

recognition by an appropriate authority that the performance of a particular institution has satisfied a prestated set of criteria.


accredited herds
cattle herds which have achieved a low level of reactors to, e.g.
 University facility with clinical treatments and evaluations occurring on site.

Tubercin is "carbohydrate complex, which is a mixture of low molecular-weight polysaccharides of an arabinomannan structure extract from Mycobacterium tuberculosis Mycobacterium tuberculosis
n.
Tubercic bacillus.


Mycobacterium tuberculosis
, is highly effective in treating various cancer patients without incurring any adverse side effects Side effects

Effects of a proposed project on other parts of the firm.
." For further information, the US Patent and Trademark Office's Official web site is retrievable at our web site: www.artec-inc.net.

Forward-looking statements in this press release, the company cautions the investors, involve risks and uncertainties pursuant to the "Safe Harbor" 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. In addition, the company cautions investors that it undertakes no obligations or responsibilities to publicly update these forward-looking statements to reflect Company's expectations with regard to these forward-looking statements or the occurrence of unanticipated events.
COPYRIGHT 2004 Business Wire
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2004, Gale Group. All rights reserved. Gale Group is a Thomson Corporation Company.

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Publication:Business Wire
Geographic Code:1USA
Date:Oct 11, 2004
Words:291
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