CLINICAL TRIALS PROFILE FOR GALAFOLD
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All Clinical Trials for galafold
Trial ID | Title | Status | Sponsor | Phase | Start Date | Summary |
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NCT00214500 ↗ | A Study of AT1001 (Migalastat Hydrochloride) in Participants With Fabry Disease | Completed | Amicus Therapeutics | Phase 2 | 2006-01-02 | Study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of migalastat hydrochloride (HCl) (migalastat) in participants with Fabry disease. |
NCT00283933 ↗ | A 24-Week Safety and Pharmacodynamic Study of AT1001 (Migalastat Hydrochloride) in Participants With Fabry Disease | Completed | Amicus Therapeutics | Phase 2 | 2006-05-09 | Study to evaluate the safety, tolerability, and pharmacodynamics of migalastat hydrochloride (HCl) (migalastat) in participants with Fabry disease. |
NCT00283959 ↗ | A 12-Week Safety and Pharmacodynamic Study of AT1001 (Migalastat Hydrochloride) in Participants With Fabry Disease | Completed | Amicus Therapeutics | Phase 2 | 2006-06-27 | Study to evaluate the safety, tolerability, and pharmacodynamics of migalastat hydrochloride (HCl) (migalastat) and how migalastat works in participants with Fabry disease. |
NCT00304512 ↗ | A 12-Week Safety and Pharmacodynamic Study of AT1001 (Migalastat Hydrochloride) in Female Participants With Fabry Disease | Completed | Amicus Therapeutics | Phase 2 | 2006-09-07 | Study to evaluate the safety, tolerability, and pharmacodynamics of migalastat hydrochloride (HCl) (migalastat) in participants with Fabry disease. |
NCT00526071 ↗ | Open-label Long-term Safety Study of AT1001 (Migalastat Hydrochloride) in Participants With Fabry Disease Who Have Completed a Previous AT1001 Study | Terminated | Amicus Therapeutics | Phase 2 | 2007-09-17 | Study to evaluate the long-term safety, tolerability, and pharmacodynamics (PD) of migalastat hydrochloride (HCl) (migalastat) in participants with Fabry disease |
NCT00925301 ↗ | Study of the Effects of Oral AT1001 (Migalastat Hydrochloride) in Patients With Fabry Disease | Completed | Amicus Therapeutics | Phase 3 | 2009-10-23 | The primary objective of this study was to compare the effect of migalastat (123 milligrams [mg] of migalastat [equivalent to 150 mg of migalastat hydrochloride]) (migalastat) versus placebo on kidney globotriaosylceramide (GL-3). |
>Trial ID | >Title | >Status | >Sponsor | >Phase | >Start Date | >Summary |
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