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SmithKline Beecham's Drug For Parkinson's Disease Clears FDA
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WESTPORT, Sep 23 (Reuters) - Ropinirole hydrochloride (Requip, SmithKline
Beecham) has been approved by the FDA for treatment of patients with
Parkinson's disease.

According to a company press release, ropinirole hydrochloride, a second
generation dopamine agonist, has been cleared for marketing both as initial
therapy for early signs and symptoms of Parkinson's disease and as
adjunctive therapy for patients with advanced Parkinson's disease who are
already taking levodopa.

"Requip is a significant advancement that may change the way physicians
treat this complicated disease," Dr. Ray Watts of Emory said in the press
release.

"Requip allows physicians to delay the use of levodopa... which may be
associated with severe motor fluctuations after long-term use."

In clinical trials, patients with mild to moderate Parkinson's disease
treated with ropinirole experienced significantly greater improvement in
motor score compared with placebo-treated patients.

In a separate trial, patients with advanced Parkinson's disease were able
to reduce their requirement for levodopa while taking ropinirole. The drug
was well-tolerated in both trials.

Westport Newsroom 203 319 2700
Copyright 1997 Reuters Limited.
<http://www.reutershealth.com/news/docs/199709/19970923rgc.html>
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