A Study to Evaluate XEN1101 as Adjunctive Therapy in Focal Epilepsy
Trial details
- Registry ID
- NCT03796962
- Phase
- Phase 2
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Research sample: selected versions from May 2023 onward plus a preceding baseline where available. Only selected fields were retained; endpoint measures were truncated to 300 characters. This is not complete trial or sponsor history. Daily snapshots begin when collection starts.
NCT05376150 · Xenon Pharmaceuticals Inc.
Text changed; whether the study measures changed has not been verified. Saved text may be shortened.
Measure: Change in Montgomery-Åsberg Depression Rating Scale (MADRS) score.
Measure: Frequency and severity of treatment-emergent adverse events (TEAEs), treatment-emergent serious adverse events (SAEs), and TEAEs leading to treatment discontinuations.
Measure: Change in Montgomery-Åsberg Depression Rating Scale (MADRS) Score.
NCT05718817 · Xenon Pharmaceuticals Inc.
Jul 2028
Apr 2033
NCT05614063 · Xenon Pharmaceuticals Inc.
Estimated
Actual
360 participants (planned)
380 participants (actual)
Estimated
Actual
Dec 2025
12 Jan 2026
Active not recruiting
Completed
NCT05716100 · Xenon Pharmaceuticals Inc.
Aug 2025
Oct 2026