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NCT00189176 · ClinicalTrials.gov registry record · Phase 1
Safety Study of Tetrathiomolybdate in Patients With Idiopathic Pulmonary Fibrosis
A Phase 1 study, sponsored by University of Michigan.
- Completed
- Registry status
- Phase 1
- Development phase
- 23
- Enrollment target
NCT00189176: Completed Phase 1 study, sponsored by University of Michigan.
NCT00189176 is a Phase 1 study that has completed, run by University of Michigan. The registered enrollment target is 23 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (62% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00189176, a Phase 1 study, has completed, sponsored by University of Michigan.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 23 participants
- Enrollment target
Study Summary
This study will evaluate the safety of the administration of a copper chelating agent, tetrathiomolybdate, for patients with idiopathic pulmonary fibrosis that have failed previous treatment. The primary endpoint for this study is safety with secondary endpoints including change in pulmonary function, exercise capacity, and quality of life.
Interventions
- DRUG Tetrathiomolybdate
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 23 participants |
| Start Date | 2003-03 |
| Est. Completion | 2006-05 |
| Phase | Phase 1 |
What the finished NCT00189176 record still lists
NCT00189176 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 23 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (62% lower).
The record links to 0 conditions, and to 1 intervention - of which Tetrathiomolybdate is the first listed.
NCT00189176 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00189176 about?
NCT00189176 is a clinical study titled "Safety Study of Tetrathiomolybdate in Patients With Idiopathic Pulmonary Fibrosis". This study will evaluate the safety of the administration of a copper chelating agent, tetrathiomolybdate, for patients with idiopathic pulmonary fibrosis that have failed previous treatment. The primary endpoint for this study is safety with secondary endpoints including change in pulmonary functio...
What is the current status of trial NCT00189176?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 23 participants. The study started on 2003-03. Estimated completion is 2006-05.
What interventions are being tested in trial NCT00189176?
The interventions under investigation include: Tetrathiomolybdate (DRUG).
Who is sponsoring clinical trial NCT00189176?
This trial is sponsored by University of Michigan, which has 1,327 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00189176's enrollment target sits among peer trials
23 1596th of 2000 higher than 400 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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