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David K. Waldman / John J. Quirk The Quigley Corporation
Lippert Heilshorn & Associates Carl Fonash
(212) 838-3777 Shareholder Relations
dwaldman@lhai.com (267) 880-1111

Quigley Provides Updates on Quigley Pharma's Business and Research Activities

- Quigley Pharma to Conduct Dose Ranging Animal Model Study for Influenza -
- Company Receives Notice of Allowance on Patent Application for Radiation Dermatitis -
- Company on Schedule with FDA Filing for Diabetic Neuropathy -

DOYLESTOWN, PA. - January 20, 2004 - The Quigley Corporation (Nasdaq: QGLY) today provided updates on key developments in its pharmaceutical business.

First, the company announced that it has re-engaged Retroscreen Virology Limited, under the direction of Professor John Oxford, to conduct two further studies. The first study is intended to repeat the previously announced results, which demonstrated QR-435 to be 100 percent effective in preventing non-infected ferrets in close proximity to an infected ferret from becoming infected with the influenza A virus.

The second study is a final dose ranging study on Quigley's QR-435 test compound. Upon dosage determination and confirmation results from this forthcoming animal model study, Quigley plans to design a human proof of concept study using a virus challenge with Influenza A virus in a quarantine unit.

As previously announced, in an independent, in vitro study conducted by Retroscreen Virology, QR-435 has demonstrated significant virucidal activity against the Urbani strain of the Severe Acute Respiratory Syndrome (SARS) virus.

Separately, Quigley announced that the company has received a "Notice of Allowance" from the United States Patent and Trademark Office for QR-335 covering "Composition and Method for Prevention, Reduction, and Treatment of Radiation Dermatitis." The company's formula QR-335 is a topical treatment to potentially prevent and relieve the effects of radiation dermatitis. A "Notice of Allowance" is sent by the Patent and Trademark Office "if, on examination, it appears that an applicant is entitled to a patent under the law."

Lastly, regarding Quigley Pharma's QR-333 and the company's intended filing with the United States Food and Drug Administration for approval of future studies for diabetic neuropathy, the company stated that it is on schedule.

Retroscreen Virology Limited is an independent research virology company affiliated with the University of London. Professor John S. Oxford, the firm's senior scientist, is Professor of Virology at St. Bartholomew's and The Royal London School of Medicine and Dentistry at the University of London. Dr. Oxford is the co-author of two standard texts on influenza and virology and has published more than 250 scientific papers throughout the world. Retroscreen specializes in developing anti-viral compounds and vaccines, and has worked with many pharmaceutical companies to assist them in developing products that now help to fight viral disease worldwide. Additional information is available on the company's website at www.retroscreen.com.

The Quigley Corporation (Nasdaq: QGLY, http://www.Quigleyco.com) is a leading developer and marketer of diversified health products including the Cold-Eeze® family of patented zinc gluconate glycine (ZIGGTM) lozenges and sugar free tablets. Cold-Eeze is the only (ZIGGTM) lozenge proven in two double-blind studies to reduce the duration of the common cold from 7.6 to 4.4 days or by 42%. In addition to Over-The-Counter (OTC) products, the company has formed Quigley Pharma Inc. (http://www.QuigleyPharma.com ), a wholly owned ethical pharmaceutical subsidiary, to introduce a line of naturally-derived patented prescription drugs. The Quigley Corporation's customers include leading national wholesalers and distributors, as well as independent and chain food, drug and mass merchandise stores and pharmacies. The Quigley Corporation makes no representation that the U.S. Food and Drug Administration or any other regulatory agency will grant an IND or take any other action to allow the aforementioned products to be studied or marketed. Furthermore, no claim is made that the potential medicine discussed here is safe, effective, or approved by the Food and Drug Administration.

Certain statements in this press release are "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995 and involve known and unknown risk, uncertainties and other factors that may cause the company's actual performance or achievements to be materially different from the results, performance or achievements expressed or implied by the forward-looking statement. Factors that impact such forward-looking statements include, among others, changes in worldwide general economic conditions, changes in interest rates, government regulations, and worldwide competition.

 

 
 
 
 


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