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NCT00778180 · ClinicalTrials.gov registry record · NA
Bioequivalence Study of Furosemide 80mg Tablets Under Fasting Conditions
A NA study, sponsored by Ranbaxy Laboratories Limited.
- Completed
- Registry status
- NA
- Development phase
- 44
- Enrollment target
NCT00778180: Completed NA study, sponsored by Ranbaxy Laboratories Limited.
NCT00778180 is a NA study that has completed, run by Ranbaxy Laboratories Limited. The registered enrollment target is 44 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00778180, a NA study, has completed, sponsored by Ranbaxy Laboratories Limited.
- COMPLETED
- Registry status
- NA
- Development phase
- 44 participants
- Enrollment target
Study Summary
The purpose of this study was to evaluate the relative bioavailability of the test formulation of furosemide 80 mg tablets (Ohm Laboratories, Inc.) with an already marketed reference formulation Lasix® (furosemide) 80 mg tablets (Aventis Pharmaceuticals NJ) under fasted conditions in healthy adult human subjects
Interventions
- DRUG furosemide 80 mg tablets
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 44 participants |
| Start Date | 2005-10 |
| Est. Completion | 2005-11 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00778180
The ClinicalTrials.gov registry entry for NCT00778180 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 44 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ranbaxy Laboratories Limited, which has 44 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which furosemide 80 mg tablets is the first listed.
NCT00778180 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00778180 about?
NCT00778180 is a clinical study titled "Bioequivalence Study of Furosemide 80mg Tablets Under Fasting Conditions". The purpose of this study was to evaluate the relative bioavailability of the test formulation of furosemide 80 mg tablets (Ohm Laboratories, Inc.) with an already marketed reference formulation Lasix® (furosemide) 80 mg tablets (Aventis Pharmaceuticals NJ) under fasted conditions in healthy adult h...
What is the current status of trial NCT00778180?
This trial is currently completed. It is a NA study. The enrollment target is 44 participants. The study started on 2005-10. Estimated completion is 2005-11.
What interventions are being tested in trial NCT00778180?
The interventions under investigation include: furosemide 80 mg tablets (DRUG).
Who is sponsoring clinical trial NCT00778180?
This trial is sponsored by Ranbaxy Laboratories Limited, which has 44 total clinical trials registered on ClinicalTrials.gov.
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