drugset / Trial / NCT06215144

Study to Evaluate NRCT-101SR in Pediatric Subjects With ADHD

NCT06215144 ↗

Phase 2/3 Terminated 95 enrolled Neurocentria, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

To evaluate the efficacy and safety of NRCT-101SR compared to placebo in subjects 13-17 years of age with ADHD

Timeline

Start
2024-01-25
Primary completion
2025-10-10
Completion
2025-11-06

Outcome

Outcome not reported

Stopped (Enrollment): “Slow enrollment”

Drugs

EvaluationDrugModalityDoseRoute
Subject NRCT-101SR Unknown 2000 mg —
Subject NRCT-101SR Unknown 2250 mg —