2 results
Approved WMOCompleted
The primary objectives of this study are: - To evaluate the efficacy of GFT505 80mg and GFT505 120mg once daily (according to adaptive design, after 6-month interim safety analysis of the 80mg data on at least 50% of patients) for 52 weeks versus…
Approved WMORecruiting
This pilot study sets out to assess stimulation-evoked PESP-BP using various stimulation protocols and to compare outcomes with PESP-BP by spontaneous ESB. Moreover, we aim to derive a stimulation protocol for PESP-BP assessment, which can be used…