CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 288 enrolled
Drug / intervention
PRC-063 oral capsules +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03618030
NCT03618030Phase 3Completed

A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Adult Laboratory Classroom Study to Evaluate the Safety and Efficacy of PRC-063 Compared to Placebo in Adults With ADHD

Purdue Pharma, Canada·interventional·Posted Aug 7, 2018·Updated Jul 26, 2021

In Brief

A Phase 3 clinical trial evaluating PRC-063 oral capsules and Placebo oral capsules for ADHD. Completed, enrolled 288 participants across 8 sites.

Detailed Summary

This is a randomized, double-blind, parallel group, placebo-controlled, dose optimized, phase 3 study to evaluate the safety and efficacy of PRC-063 in the treatment of ADHD in adults

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsADHD
CountriesUnited States
Collaborators--

Timeline

Phase 3CompletedFinished
20192020202120222023202420252026
First PostedAug 7, 2018
Enrollment StartAug 21, 2018
Primary CompletionJul 5, 2019
TodayJul 2, 2026
Enrollment to primary: 10 monthsPosted 7.9 years ago

Interventions

PRC-063 oral capsulesdrug

Daily dose

Placebo oral capsulesdrug

Daily dose