Merck Serono announced today the initiation of the SETTLE(1) study. This study will evaluate the efficacy and safety of a dose range of safinamide (50-100 mg once daily) as add-on therapy to a stable dose of levodopa, in mid- to late-stage Parkinson's disease patients with motor fluctuations compared to placebo.
The SETTLE study is one of the Phase III trials that constitute the clinical development program designed to support an application for marketing authorization as discussed with regulatory authorities. SETTLE is a six-month (24-week), randomized, double-blind, international Phase III trial. The trial will involve more than 450 patients with mid- to late-stage idiopathic Parkinson's disease (more than five years of disease duration) treated with a stable dose of levodopa for at least four weeks who have motor fluctuations with more than one and a half hours of "OFF"(2) time during the day. Additionally, patients may be receiving concomitant treatment with stable doses of a dopamine agonist, a COMT inhibitor, an anticholinergic and/or amantadine. After a four-week levodopa dosage stabilization phase, study participants will be randomized in one of the two arms of the trial (1:1) to receive either safinamide or matching placebo tablets, as adjunctive treatment to levodopa therapy.
The primary endpoint of the trial is the change in daily "ON" time, as assessed by the recordings of diary cards maintained by patients after prior training, from baseline to week 24. Secondary endpoints include changes in measures of activities of daily living, global clinical status and health-related quality of life.
"Managing motor fluctuations and reducing the time during which anti-Parkinson drugs are not working and symptoms return, the so-called 'OFF' times, are still unmet medical needs for patients with mid- to late-stage Parkinson's disease," said Bernhard Kirschbaum, Merck Serono's Head of Global Research and Development. "After the encouraging results we obtained for study 016, we aim to confirm the efficacy of safinamide as an add-on therapy to levodopa in a flexible dosing regimen."
Additional results from the analyses of study 016
Additional results from the analyses of study 016 (for which top-line data were reported previously, showing that safinamide significantly improved motor function in patients with advanced Parkinson's disease) are now available and will be shared in detail at the Movement Disorder Society's 13th International Congress in Paris in June: safinamide was shown to have a significant benefit on motor fluctuations (increase in "ON" time, decrease in "OFF" time) at both 50 and 100 mg doses without any increase in "ON" time with troublesome dyskinesias. A statistically significant reduction in the UPDRS(3) part IV scale was seen at both doses. The 100 mg dose was also shown to improve depressive symptoms in this non-depressed patient population as measured by the GRID-HAMD(4) scale total score, and to result in an improvement of the emotional well-being as measured by a subscale of the PDQ-39(5).
"The additional results from study 016 are encouraging and suggest that safinamide could have benefits beyond motor symptoms, motor fluctuations and activities of daily living. The increase in 'ON' time without any increase in troublesome dyskinesia is critical for patients and physicians," said Ravi Anand, Newron's Chief Medical Officer. "Depressive symptoms are important aspects of PD and the ability of safinamide to improve some of these symptoms in addition to the other benefits is promising and warrants further studying safinamide as a potential new treatment option."
Merck Serono has exclusive worldwide rights to develop, manufacture and commercialize safinamide in Parkinson's disease, Alzheimer's disease and other therapeutic applications, as per the agreement signed with Newron in 2006.
Footnotes
(1) SETTLE: SafinamidE Treatment as add-on To LEvodopa in idiopathic Parkinson's disease with motor fluctuations