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NCT01013142 · ClinicalTrials.gov registry record · Phase 1
Evaluate the Safety of MN-221 in Subjects With Stable Moderate to Severe Chronic Obstructive Pulmonary Disease (COPD)
A Phase 1 study, sponsored by MediciNova.
- Completed
- Registry status
- Phase 1
- Development phase
- 48
- Enrollment target
NCT01013142: Completed Phase 1 study, sponsored by MediciNova.
NCT01013142 is a Phase 1 study that has completed, run by MediciNova. The registered enrollment target is 48 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (20% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01013142, a Phase 1 study, has completed, sponsored by MediciNova.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 48 participants
- Enrollment target
Study Summary
The objective of this clinical study is to determine the safety of intravenous MN-221 compared to placebo when administered in subjects diagnosed with stable moderate to severe COPD.
Interventions
- DRUG MN-221 (Dose Group 1)
- DRUG MN-221 (Dose Group 2)
- DRUG MN-221 (Dose Group 3)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 48 participants |
| Start Date | 2009-11 |
| Est. Completion | 2010-03 |
| Phase | Phase 1 |
What the finished NCT01013142 record still lists
NCT01013142 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 48 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (20% lower).
The record links to 0 conditions, and to 3 interventions - of which MN-221 (Dose Group 1) is the first listed.
NCT01013142 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01013142 about?
NCT01013142 is a clinical study titled "Evaluate the Safety of MN-221 in Subjects With Stable Moderate to Severe Chronic Obstructive Pulmonary Disease (COPD)". The objective of this clinical study is to determine the safety of intravenous MN-221 compared to placebo when administered in subjects diagnosed with stable moderate to severe COPD.
What is the current status of trial NCT01013142?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 48 participants. The study started on 2009-11. Estimated completion is 2010-03.
What interventions are being tested in trial NCT01013142?
The interventions under investigation include: MN-221 (Dose Group 1) (DRUG), MN-221 (Dose Group 2) (DRUG), MN-221 (Dose Group 3) (DRUG).
Who is sponsoring clinical trial NCT01013142?
This trial is sponsored by MediciNova, which has 17 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01013142's enrollment target sits among peer trials
48 1025th of 2000 higher than 948 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 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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