ID
25951
Description
Investigators Statement Ropinirole Case Report Form GSK Study ID: 100013 Clinical Study ID: RRL100013 A 12-Week, Double-Blind, Placebo-Controlled, Twice-Daily Dosing Study to Assess the Efficacy and Safety of Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS) Requiring Extended Treatment Coverage
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Versions (1)
- 10/1/17 10/1/17 -
Copyright Holder
gsk
Uploaded on
October 1, 2017
DOI
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License
Creative Commons BY-NC 3.0
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Investigators Statement Ropinirole Case Report Form GSK RRL100013
Investigators Statement Ropinirole Case Report Form GSK RRL100013
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