Post-hoc analysis of a 52-week phase 3 trial showed subcutaneous foslevodopa/foscarbidopa infusion reduced OFF time and increased ON time without dyskinesia similarly in patients with and without prior DBS, with overall comparable safety but a higher rate of severe treatment-emergent adverse events…
Provides strong translational value by supporting a non-surgical, continuous levodopa/carbidopa option for advanced PD regardless of DBS history, helping guide clinical decision-making and safety monitoring for post-DBS patients.