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NCT00474136 · ClinicalTrials.gov registry record · Phase 1
Study to Compare the Pharmacokinetics of IV Diclofenac Sodium (2 Doses)Versus Oral Diclofenac Potassium
A Phase 1 study, sponsored by Javelin Pharmaceuticals.
- Completed
- Registry status
- Phase 1
- Development phase
- 36
- Enrollment target
NCT00474136: Completed Phase 1 study, sponsored by Javelin Pharmaceuticals.
NCT00474136 is a Phase 1 study that has completed, run by Javelin Pharmaceuticals. The registered enrollment target is 36 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (40% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00474136, a Phase 1 study, has completed, sponsored by Javelin Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 36 participants
- Enrollment target
Study Summary
The purpose of this study is to assess the pharmacokinetic parameters of intravenous diclofenac sodium (DIC075V) 18.75 mg and 37.5 mg following single- and multiple-dose administration, as compared to oral diclofenac potassium (Cataflam® 50 mg), the approved reference product.
Interventions
- DRUG Intravenous diclofenac sodium (DIC075V) 18.75 mg
- DRUG Intravenous diclofenac sodium (DIC075V) 37.5 mg
- DRUG Oral diclofenac potassium 50 mg
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 36 participants |
| Start Date | 2007-03 |
| Est. Completion | 2007-05 |
| Phase | Phase 1 |
What the finished NCT00474136 record still lists
NCT00474136 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 36 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (40% lower).
The record links to 0 conditions, and to 3 interventions - of which Intravenous diclofenac sodium (DIC075V) 18.75 mg is the first listed.
NCT00474136 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00474136 about?
NCT00474136 is a clinical study titled "Study to Compare the Pharmacokinetics of IV Diclofenac Sodium (2 Doses)Versus Oral Diclofenac Potassium". The purpose of this study is to assess the pharmacokinetic parameters of intravenous diclofenac sodium (DIC075V) 18.75 mg and 37.5 mg following single- and multiple-dose administration, as compared to oral diclofenac potassium (Cataflam® 50 mg), the approved reference product.
What is the current status of trial NCT00474136?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 36 participants. The study started on 2007-03. Estimated completion is 2007-05.
What interventions are being tested in trial NCT00474136?
The interventions under investigation include: Intravenous diclofenac sodium (DIC075V) 18.75 mg (DRUG), Intravenous diclofenac sodium (DIC075V) 37.5 mg (DRUG), Oral diclofenac potassium 50 mg (DRUG).
Who is sponsoring clinical trial NCT00474136?
This trial is sponsored by Javelin Pharmaceuticals, which has 9 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00474136's enrollment target sits among peer trials
36 1210th of 2000 higher than 743 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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