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NCT02363998 · ClinicalTrials.gov registry record · Phase 3
Open-Label, Safety Study of Lofexidine
A Phase 3 study, sponsored by USWM, LLC (dba US WorldMeds).
- Completed
- Registry status
- Phase 3
- Development phase
- 286
- Enrollment target
NCT02363998: Completed Phase 3 study, sponsored by USWM, LLC (dba US WorldMeds).
NCT02363998 is a Phase 3 study that has completed, run by USWM, LLC (dba US WorldMeds). The registered enrollment target is 286 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (63% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02363998, a Phase 3 study, has completed, sponsored by USWM, LLC (dba US WorldMeds).
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 286 participants
- Enrollment target
Study Summary
The purpose of this Phase 3 open-label treatment study is to evaluate the safety and effectiveness of lofexidine at a clinically relevant dose to alleviate symptoms of acute withdrawal from any opioid, including methadone and buprenorphine. This study will take place in a variety of clinical scenarios, both in-clinic and outpatient settings.
Primary Outcome
Subjects with at least 1 TEAE occurring on days 1-14.
Interventions
- DRUG Lofexidine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 286 participants |
| Start Date | 2015-02 |
| Est. Completion | 2015-10 |
| Phase | Phase 3 |
What the finished NCT02363998 record still lists
NCT02363998 is an interventional study that assigns participants to a tested intervention. The registered 286 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (63% lower).
The record links to 0 conditions, and to 1 intervention - of which Lofexidine is the first listed.
NCT02363998 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02363998 about?
NCT02363998 is a clinical study titled "Open-Label, Safety Study of Lofexidine". The purpose of this Phase 3 open-label treatment study is to evaluate the safety and effectiveness of lofexidine at a clinically relevant dose to alleviate symptoms of acute withdrawal from any opioid, including methadone and buprenorphine. This study will take place in a variety of clinical scenari...
What is the current status of trial NCT02363998?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 286 participants. The study started on 2015-02. Estimated completion is 2015-10.
What interventions are being tested in trial NCT02363998?
The interventions under investigation include: Lofexidine (DRUG).
Who is sponsoring clinical trial NCT02363998?
This trial is sponsored by USWM, LLC (dba US WorldMeds), which has 16 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02363998's enrollment target sits among peer trials
286 1182nd of 2000 higher than 816 of 2,000 other Phase 3 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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