ADVR Announces the Completion of Patient Enrollment in its Phase I/II Clinical Trial in AIDS Business Wire
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ADVR Announces the Completion of Patient Enrollment in its Phase I/II Clinical Trial in AIDS

Business Wire - August 9, 2004


YONKERS, N.Y.-- Advanced Viral Research Corp. announced today that all 30 patients have been enrolled in its Phase I/II clinical trial of AVR118 in patients with AIDS, thereby completing patient enrollment in this trial. This Phase I/II trial is being conducted at the Kaplan Medical Center in Israel in cachectic AIDS patients who may or may not be receiving anti-retroviral or highly active anti-retroviral therapy.

ADVR's AVR118 represents a biopolymer that possesses novel immunomodulator activity. This peptide-nucleic acid complex, which to date has demonstrated a very favorable safety profile, appears to stimulate the proinflammatory responses required to combat viral infections such as AIDS and human papillomavirus and to dampen aberrant autoimmune-type inflammatory responses, such as occur in patients with rheumatoid arthritis.

For further information regarding Advanced Viral Research Corp., please visit our website at www.adviral.com. ADVR, based in Yonkers, New York, is a biopharmaceutical firm dedicated to improving patients' lives by researching, developing and bringing to market new and effective therapies for viral and other diseases.

Note: This news release contains forward-looking statements that involve risks associated with clinical development, regulatory approvals, including application to the FDA, product commercialization and other risks described from time to time in the SEC reports filed by the Company. AVR118 (Product R) is not approved by the U.S. Food and Drug Administration or any comparable agencies of any other countries. There is no assurance that the Company will be able to secure the financing necessary to continue and/or complete the clinical trials of AVR118 or satisfy certain other conditions relating to clinical trials including obtaining adequate insurance on terms acceptable to the Company or that if completed, clinical trials performed outside the United States will assist the Company in obtaining FDA or other regulatory approval. . The Company undertakes no obligation to update or revise the information contained in this announcement whether as a result of new information, future events or circumstances or otherwise.

CONTACT: CWR & Partners, LLP

Ronnie Welch, 508-222-4802

Ronnie@cwrpartners.com

SOURCE: Advanced Viral Research Corp.


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