Schering-Plough Reports Long-Term Vicriviroc Data From Phase II Open-Label Extension Study in Treatment-Experienced HIV-Infecte...(e Private Securities Litigation Reform A...),Health

Date:9/14/2009

e Private Securities Litigation Reform Act of 1995, including statements relating to the company's clinical development plans and the potential for vicriviroc. Forward-looking statements relate to expectations or forecasts of future events. Schering-Plough does not assume the obligation to update any forward-looking statement. Many factors could cause actual results to differ materially from Schering-Plough's forward-looking statements, including uncertainties in the regulatory process, among other uncertainties. For further details about these and other factors that may impact the forward-looking statements, see Schering-Plough's Securities and Exchange Commission filings, including Part II, Item 1A. "Risk Factors" in the Company's second quarter 2009 10-Q, filed July 24, 2009.

Endnotes

(1) McCarthy M, Suleiman J, Diaz R, et al. Vicriviroc Long-Term Safety and Efficacy: 96-Week Results from the VICTOR-E1 Study. 49th Annual Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC); Sept. 12-15, 2009; San Francisco, CA, USA; No. H-923.

(2) Coakley E, et al. Second International Workshop Targeting HIV Entry. Oct. 20-21, 2006; Boston, MA, USA; No. 8.

(3) Hoffmann C (2007) The epidemiology of HIV coreceptor tropism. Eur J Med Res (2007) 12: 385-390.

(4) Atazanavir sulfate is a Bristol-Myers Squibb Company prescription medicine. Please see the atazanavir product insert for information on this product.

(5) Truvada is a registered trademark of Gilead Sciences, Inc. Please see the Truvada product insert for information on this product.

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