CLINICAL TRIALS PROFILE FOR XADAGO
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All Clinical Trials for xadago
Trial ID | Title | Status | Sponsor | Phase | Start Date | Summary |
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NCT02495831 ↗ | Drug Interaction Study of Safinamide and a BCRP Substrate, Diclofenac, Concomitantly Administered to Healthy Volunteers | Completed | Cross Research S.A. | Phase 1 | 2015-05-01 | To evaluate if a single dose of safinamide 200 mg has an effect on the pharmacokinetics of diclofenamic acid, concomitantly administered as a single 50 mg diclofenac sodium dose, with respect to 50 mg diclofenac sodium administered alone. |
NCT02495831 ↗ | Drug Interaction Study of Safinamide and a BCRP Substrate, Diclofenac, Concomitantly Administered to Healthy Volunteers | Completed | Zambon SpA | Phase 1 | 2015-05-01 | To evaluate if a single dose of safinamide 200 mg has an effect on the pharmacokinetics of diclofenamic acid, concomitantly administered as a single 50 mg diclofenac sodium dose, with respect to 50 mg diclofenac sodium administered alone. |
NCT03216304 ↗ | Safinamide Steady State Interaction With Rosuvastatin | Completed | Zambon SpA | Phase 1 | 2017-05-22 | To evaluate if safinamide at the steady state, obtained after multiple 100 mg once a day administrations, has an effect on the pharmacokinetics of rosuvastatin, concomitantly administered as a single 20 mg dose, with respect to the pharmacokinetics of 20 mg rosuvastatin administered alone. |
NCT03216304 ↗ | Safinamide Steady State Interaction With Rosuvastatin | Completed | Cross Research S.A. | Phase 1 | 2017-05-22 | To evaluate if safinamide at the steady state, obtained after multiple 100 mg once a day administrations, has an effect on the pharmacokinetics of rosuvastatin, concomitantly administered as a single 20 mg dose, with respect to the pharmacokinetics of 20 mg rosuvastatin administered alone. |
NCT03753763 ↗ | Safinamide for Multiple System Atrophy (MSA) | Completed | Zambon SpA | Phase 2 | 2019-10-29 | The study is a placebo controlled study, with two parallel arms, in which participants will be randomly assigned in a 2:1 ratio to receive either active (200 mg safinamide) or placebo in a double blind manner. Study population is patients diagnosed, with possible or probable parkinsonian variant of Multiple System Atrophy who are on a stable treatment of levodopa |
>Trial ID | >Title | >Status | >Sponsor | >Phase | >Start Date | >Summary |
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