A Clinical Trial of PRAX-944 in Participants With Essential Tremor
Trial details
- Registry ID
- NCT05021978
- Phase
- Phase 2
Company identity has not yet been verified
Browse linked trials and recorded changes, or follow this company for updates.
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.
NCT06999902 · Praxis Precision Medicines
Estimated
Actual
count: 230; type: ESTIMATED
count: 255; type: ACTUAL
Estimated
Actual
2025-11-24
2026-05-14
Recruiting
Completed
NCT07010471 · Praxis Precision Medicines
Recruiting
Active not recruiting
NCT07505004 · Praxis Precision Medicines
Recruiting
Active not recruiting
NCT07019922 · Praxis Precision Medicines
2026-06
2026-12
NCT06087276 · Praxis Precision Medicines
Estimated
Actual
2025-09
2025-10-10
Enrolling by invitation
Active not recruiting
NCT07019922 · Praxis Precision Medicines
count: 50; type: ESTIMATED
count: 40; type: ESTIMATED
NCT07010471 · Praxis Precision Medicines
2026-07
2026-12
NCT05818553 · Praxis Precision Medicines
measure: To assess the effect of PRAX-562 on the frequency of countable motor seizures in pediatric participants with DEEs
measure: PART A (Cohorts 1 and 2) RDB: To evaluate the safety and tolerability of PRAX 562 in pediatric participants with SCN2A- and SCN8A- DEEs; measure: PART B (Cohorts 1 and 2) OLE: To evaluate the long-term safety and tolerability of PRAX-562 in pediatric participants with DEEs
The saved outcome text may be shortened. Check the source for full wording.
count: 100; type: ESTIMATED
count: 77; type: ESTIMATED
Estimated
Actual
2026-03-23
2025-11-12
Recruiting
Active not recruiting
NCT07010471 · Praxis Precision Medicines
2026-04
2026-07
NCT06087276 · Praxis Precision Medicines
measure: Parallel Design: Change from Baseline (CFB) to Week 12 (Day 84) on mADL11; measure: Randomized Withdrawal: The proportion of participants that maintain response, as defined by change in mADL11 score, following randomized withdrawal; measure: Long-term Safety Study: Number of participants with Adverse Events (AE) and their severity.
measure: Parallel Design: Change from Baseline (CFB) to Week 8 (Day 56) on mADL11 score; measure: Randomized Withdrawal: The proportion of participants that maintain response, as defined by change in mADL11 score, following randomized withdrawal; measure: Long-term Safety Study: Number of participants with Adverse Events (AE) and their severity.
The saved outcome text may be shortened. Check the source for full wording.
count: 600; type: ESTIMATED
count: 1000; type: ESTIMATED
2024-09
2025-09
Recruiting
Enrolling by invitation