Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT00888004Phase 2Completed
Phase 2, randomised, double-blind trial in dyskinesia comparing AFQ056 + L-dopa with Placebo + L-dopa (2 arms). Primary endpoints: modified Abnormal Involuntary Movement Scale at 20 days, Safety and Tolerability at 20 days and 1 more. Started Mar 2009; status: completed.
Beyond the preview
Study design, results and competitive context are available in the Gosset platform where reported.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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