AEGiS-PRn: Zerit(R) (stavudine) Approved For First-Line Treatment of HIV in Europe; Indication Includes Adults and Children PRNewswireImportant note: Information in this article was accurate in 1997. The state of the art may have changed since the publication date.
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Zerit(R) (stavudine) Approved For First-Line Treatment of HIV in Europe; Indication Includes Adults and Children

PR Newswire, 810 Seventh Avenue, New York, NY 10019 - Monday August 25 7:00 PM EDT


PRINCETON, N.J., Aug. 25 /PRNewswire/ -- Bristol-Myers Squibb Company (NYSE:BMY) today announced that Zerit(R) (stavudine), also known as d4T, received approval by the European Union for use in combination therapy in the first-line treatment of HIV, the virus that causes AIDS, in Europe.

The decision was based on recent data from clinical trials using Zerit in adults and children which demonstrate that combinations that include d4T can reduce viral load, often to undetectable levels, and increase the body's infection-fighting CD4 cells. Both are proven markers of disease improvement.

Bristol-Myers Squibb is one of the leading companies in the research and development of HIV treatments. In addition to Zerit, the company markets VIDEX(R) (didanosine), also known as ddI, for treating HIV. Bristol-Myers Squibb is also developing two protease inhibitors for the treatment of HIV.

Zerit has been available in the U.S. since June 1994 and in Europe since May 1996, and is available in several other countries worldwide. In the U.S., Zerit is indicated for the treatment of HIV-infected patients who have received prolonged prior AZT (zidovudine) therapy. The most notable clinical toxicity of Zerit is peripheral neuropathy, which usually resolves if treatment is withdrawn. Resumption of treatment may be considered at a reduced dose.

VIDEX has been on the market in the U.S. since 1991 and is available worldwide. VIDEX is indicated for the first-line treatment of HIV infection when antiretroviral therapy is warranted. The most common adverse events associated with VIDEX are diarrhea and peripheral neuropathy. Both Zerit and VIDEX are now available for the treatment of children with AIDS.

Bristol-Myers Squibb also markets TAXOL(R) (paclitaxel) injection for AIDS-related Kaposi's sarcoma, Megace(R) (megestrol acetate) Oral Suspension for HIV anorexia/cachexia, and Fungizone(R) (amphotericin B) Oral Suspension for oral candidiasis in HIV-infected patients.

Bristol-Myers Squibb is a diversified worldwide health and personal care company whose principal businesses are pharmaceuticals, consumer products, nutritional and medical devices. It is a leading maker of innovative therapies for cardiovascular, metabolic and infectious diseases, central nervous system and dermatological disorders, and cancer. The company is a leader in consumer medicines, orthopaedic devices, ostomy care, wound management, nutritional supplements, infant formulas, and hair and skin products.

Visit Bristol-Myers Squibb on the World Wide Web at : http:/www.bms.com

SOURCE: Bristol-Myers Squibb Company

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Always watch for outdated information. This article first appeared in 1997. This material is designed to support, not replace, the relationship that exists between you and your doctor.

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