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NCT00725881 · ClinicalTrials.gov registry record · Phase 1
Safety, Efficacy, and Pharmacokinetics (PK) Study of Trans Sodium Crocetinate (TSC) in Patients With Intermittent Claudication
A Phase 1 study, sponsored by Diffusion Pharmaceuticals.
- Completed
- Registry status
- Phase 1
- Development phase
- 48
- Enrollment target
NCT00725881: Completed Phase 1 study, sponsored by Diffusion Pharmaceuticals.
NCT00725881 is a Phase 1 study that has completed, run by Diffusion Pharmaceuticals. 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
NCT00725881, a Phase 1 study, has completed, sponsored by Diffusion Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 48 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the safety and pharmacokinetics of multiple, once-daily, intravenous doses of trans sodium crocetinate (TSC). The effectiveness of TSC in alleviating the symptoms of intermittent claudication (IC) will also be assessed.
Interventions
- DRUG Trans sodium crocetinate (TSC)
- DRUG 0.9% normal saline
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 48 participants |
| Start Date | 2008-08 |
| Est. Completion | 2010-03 |
| Phase | Phase 1 |
What the finished NCT00725881 record still lists
NCT00725881 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 2 interventions - of which Trans sodium crocetinate (TSC) is the first listed.
NCT00725881 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00725881 about?
NCT00725881 is a clinical study titled "Safety, Efficacy, and Pharmacokinetics (PK) Study of Trans Sodium Crocetinate (TSC) in Patients With Intermittent Claudication". The purpose of this study is to evaluate the safety and pharmacokinetics of multiple, once-daily, intravenous doses of trans sodium crocetinate (TSC). The effectiveness of TSC in alleviating the symptoms of intermittent claudication (IC) will also be assessed.
What is the current status of trial NCT00725881?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 48 participants. The study started on 2008-08. Estimated completion is 2010-03.
What interventions are being tested in trial NCT00725881?
The interventions under investigation include: Trans sodium crocetinate (TSC) (DRUG), 0.9% normal saline (DRUG).
Who is sponsoring clinical trial NCT00725881?
This trial is sponsored by Diffusion Pharmaceuticals, which has 8 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00725881'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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