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Clinical Trials associated with S-606001 / Not yet recruitingPhase 2 A Phase 2, Multicenter, Randomized, Placebo-controlled, Double-blind Study to Investigate the Safety, Pharmacodynamics, and Preliminary Efficacy of S-606001 as an Add-on to Enzyme Replacement Therapy in Patients With Late-onset Pompe Disease
The purpose of this study is to evaluate the safety, pharmacodynamics (PD), and exploratory clinical efficacy of S-606001 in adult participants with LOPD as an add-on to ERT.
A Phase 1, crossover, open-label study to compare the bioavailability of S-606001 between capsules and tablets and to investigate the food effect with the tablets following a single oral dose in healthy adults aged 18 to 55 years
Start Date04 Jul 2024 |
Sponsor / Collaborator- |
100 Clinical Results associated with S-606001
100 Translational Medicine associated with S-606001
100 Patents (Medical) associated with S-606001
100 Deals associated with S-606001