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BioQuest Inc. Announces M. Ross Johnson, Ph.D. Joins BioQuest Inc.


HOUSTON--(BW HealthWire)--July 6, 1999--

BioQuest Inc. (OTC OTC

See: Over-the-counter.


OTC

See over-the-counter market (OTC).
 BB:HIVX) announced today that M. Ross Johnson, Ph.D. has joined the company as special advisor to the Board of Directors. Dr. Johnson, formerly president and chief executive officer of Trimeris Inc. (Nasdaq:TRMS) of Durham, N.C., will advise BioQuest on drug development, 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.
 regulatory matters, corporate partnership opportunities, capital formation, and technology acquisition and development.

Dr. Johnson, best known for his expertise in analgetic receptor technology, enjoyed a twenty-year career in drug development with Pfizer and Glaxo. He is a discoverer of the ultra-short acting analgetic/anesthetic remifentanil (ULTIVA((R))), the oral anti-diabetic englitazone, and the prostaglandin analog sulprostone. His resume includes over one hundred patents and two hundred peer-review publications and invited lecture presentations. Dr. Johnson serves on numerous boards including the Board of the Inter-company Collaboration for AIDS and is the incoming Chair of the Division of Organic Chemistry of the American Chemical Society The American Chemical Society (ACS) is a learned society (professional association) based in the United States that supports scientific inquiry in the field of chemistry. Founded in 1876 at New York University, the ACS currently has over 160,000 members at all degree-levels and in .

At Trimeris from 1995 to 1999, Dr. Johnson served first as chief scientific officer, and then in March, 1996 was promoted to president and chief executive officer. During his tenure, Trimeris transitioned from small private company to public company with Trimeris' HIV HIV (Human Immunodeficiency Virus), either of two closely related retroviruses that invade T-helper lymphocytes and are responsible for AIDS. There are two types of HIV: HIV-1 and HIV-2. HIV-1 is responsible for the vast majority of AIDS in the United States.  fusion inhibitor progressing from the discovery stage to FDA Phase II, obtaining FDA Fast Track Fast Track is a designation of the Food and Drug Administration that accelerates the approval of experimental drugs, such as experimental cancer treatments, that treat a serious or life-threatening medical condition for which no other drug either exists or works as well.  designation in the process.

Warren C. Lau, president of BioQuest Inc. stated, "Ross Johnson brings a unique set of qualifications to BioQuest Inc. It would be difficult to imagine a better person to help the company drive our projects, especially our R15K HIV blocking agent, through to commercialization."

BioQuest Inc. is a biotechnology development company in the field of HIV/AIDS HIV/AIDS Human Immunodeficiency Virus/Acquired Immune Deficiency Syndrome  therapy, prophylaxis, and vaccine. BioQuest's lead compound is R15K, a blocking agent designed to prevent HIV from entering and infecting human immune system cells. In laboratory testing and in mice, rhesus monkeys, and chimpanzees it has shown encouraging results and is being readied to enter FDA human testing.

In the pipeline are two more approaches to treatment and prevention of HIV/AIDS. The patented compound S4S has been shown in vitro to be able to attack and disable the very proteins HIV uses to bind to to contract; as, to bind one's self to a wife s>.

See also: Bind
 and infect human immune system cells, thus rendering HIV non-infectious. Finally, BioQuest's patented Antibody-negative Cell Mediated Immunity Vaccine is now undergoing testing in rhesus monkeys using a "chimeric" Simian/Human Immunodeficiency Virus. This trial is currently producing data that, if confirmed in subsequent testing, represent exciting proof of principle.

This press release contains certain forward looking statements within the meaning of 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. Such statements are made based on management's current expectations and beliefs. Actual results may vary from those currently anticipated based upon a number of factors, including uncertainties inherent in the drug development process, the timing and success of clinical trials, and the receipt of necessary approvals from the United States Food and Drug Administration United States Food and Drug Administration (FDA),
n.pr a unit of the Public Health Service created to protect the health of the nation against impure and unsafe foods, drugs, and cosmetics.
. The company undertakes no obligation to release publicly any revisions which may be made to reflect events or circumstances after the date hereof.
COPYRIGHT 1999 Business Wire
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 1999, Gale Group. All rights reserved. Gale Group is a Thomson Corporation Company.

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Publication:Business Wire
Geographic Code:1USA
Date:Jul 6, 1999
Words:513
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