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writingreview and editing, QL and NhZ

, & Rittmann, S

There was a larger change in the mean HRR at 60 s in the pooled BAY 2413555 treatment arms in Part A (1.25 mg) compared to the placebo (+ 7.3 vs

As for LV-GCH1-TH-AADC, results of a phase I/II trial with two study sites (France and UK) showed long-term safety and tolerability of ProSavin , as well motor symptom improvement, as assessed with the UPDRS part 3 motor score

Results can vary depending on various factors such as individual metabolism and dosage

Gopinath, V
