drugset / Trial / NCT05683249

Study to Evaluate NRCT-101SR in Adult Attention Deficit Hyperactivity Disorder (ADHD)

NCT05683249 ↗

Phase 2/3 Completed 223 enrolled Neurocentria, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The goal of this clinical trial is to evaluate the efficacy and safety of NRCT-101SR compared to placebo in adult patients with ADHD aged 18 years and older.

Timeline

Start
2023-02-25
Primary completion
2024-01-17
Completion
2024-01-17

Drugs

EvaluationDrugModalityDoseRoute
Subject NRCT-101SR Unknown 1500 mg Oral
Subject NRCT-101SR Unknown 2000 mg Oral