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Schering-Plough Reports Financial Results for Third Quarter of 2007
Date:10/22/2007

tional CCR5 antagonist, administered

once-daily in combination with an optimized background therapy in adult

treatment-experienced HIV patients with R5-type virus only. (Announced

Sept. 17)

-- Reported that the Committee for Medicinal Products for Human Use (CHMP)

of the European Medicines Agency (EMEA) had issued a positive opinion

recommending approval of combination therapy with PEGINTRON

(peginterferon alfa-2b) and REBETOL (ribavirin) for retreating adult

patients with chronic hepatitis C whose previous treatment with

interferon alpha (pegylated or non-pegylated) and ribavirin combination

therapy or interferon alpha monotherapy did not result in a sustained

response. (Announced Sept. 24)

-- Received approval from the European Commission for Schering-Plough's

planned acquisition of Organon BioSciences N.V. from Akzo Nobel N.V.

(Announced Oct. 11)

-- Provided an update on the clinical development program for boceprevir,

the company's investigational oral hepatitis C protease inhibitor. In

a Phase II study in treatment-nave hepatitis C patients, boceprevir

combination therapy with PEGINTRON and REBETOL achieved a high rate of

early virologic response. In a second study in treatment non

responders (the most difficult-to-treat patient population), while

boceprevir combination therapy with PEGINTRON and REBETOL demonstrated

antiviral activity, the majority of patients did not achieve a

sustained virologic response (SVR). No increase in skin adverse events

(rash) beyond what was seen in the control group was observed in these

studies. (Announced Oct. 18)

Third Quarter 2007 Conference Call and Webcast

Schering-Plough will conduct a conference call today at 8 a.m. (EDT) to review the 2007 third quarter results. To listen live to the call, di
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SOURCE Schering-Plough Corporation
Copyright©2007 PR Newswire.
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