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COMPLETED Phase 3

PRC-063 in an ADULT Workplace Environment

NCT02225639 · View on ClinicalTrials.gov ↗

Study Summary

The primary objective of this study is to assess the time of onset and time course of efficacy over 16 hours of PRC-063 compared to placebo in adults diagnosed with ADHD in a simulated adult workplace environment (AWE) setting, as measured by the PERMP (an individually-adjusted math test) at pre-dose, 1.0, 2.0, 5.0, 8.0, 11.0, 14.0 and 16.0 hours post-dose.

Interventions

  • DRUG Placebo
  • DRUG PRC-063 25 mg
  • DRUG PRC-063 45 mg
  • DRUG PRC-063 35 mg
  • DRUG PRC-063 55 mg

Study Locations (2)

California

  • AVIDA, Inc. — Newport Beach

Nevada

  • Center for Psychiatry and Behavioral Medicine Inc. — Las Vegas

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2014-08
Est. Completion 2015-05
Phase Phase 3

Sponsor

Rhodes Pharmaceuticals, L.P.

3 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02225639

The ClinicalTrials.gov registry entry for NCT02225639 describes a study currently listed as completed. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Rhodes Pharmaceuticals, L.P., which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Attention Deficit Hyperactivity Disorder (ADHD) appearing as the primary indexed condition, and to 5 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02225639 reports 2 study locations spanning 2 distinct geographic areas — top geographies include California, Nevada. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT02225639 about?

NCT02225639 is a clinical study titled "PRC-063 in an ADULT Workplace Environment". The primary objective of this study is to assess the time of onset and time course of efficacy over 16 hours of PRC-063 compared to placebo in adults diagnosed with ADHD in a simulated adult workplace environment (AWE) setting, as measured by the PERMP (an individually-adjusted math test) at pre-dos...

What is the current status of trial NCT02225639?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 60 participants. The study started on 2014-08. Estimated completion is 2015-05.

What conditions does trial NCT02225639 study?

This clinical trial studies the following conditions: Attention Deficit Hyperactivity Disorder (ADHD). These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02225639?

The interventions under investigation include: Placebo (DRUG), PRC-063 25 mg (DRUG), PRC-063 45 mg (DRUG), PRC-063 35 mg (DRUG), PRC-063 55 mg (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02225639?

This trial is sponsored by Rhodes Pharmaceuticals, L.P., which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02225639 being conducted?

This trial has 2 study locations across California, Nevada. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial