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NCT00835042 · ClinicalTrials.gov registry record · Phase 1
Moexipril HCL/Hydrochlorothiazide 15/25 mg Tablets Under Fasting Conditions
A Phase 1 study, sponsored by Teva Pharmaceuticals USA.
- Completed
- Registry status
- Phase 1
- Development phase
- 60
- Enrollment target
NCT00835042: Completed Phase 1 study, sponsored by Teva Pharmaceuticals USA.
NCT00835042 is a Phase 1 study that has completed, run by Teva Pharmaceuticals USA. The registered enrollment target is 60 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00835042, a Phase 1 study, has completed, sponsored by Teva Pharmaceuticals USA.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 60 participants
- Enrollment target
Study Summary
The objective of this study is to compare the relative bioavailability of Moexipril HCl/hydrochlorothiazide 15/25 mg tablets (manufactured and distributed by TEVA Pharmaceuticals USA) with that of UNIRETIC® 15/25 mg tablets (Schwartz Pharma) in healthy, adult non-smoking subjects under fasting conditions.
Interventions
- DRUG Moexipril HCl/hydrochlorothiazide 15/25 mg tablets
- DRUG UNIRETIC® 15/25 mg tablets
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2003-10 |
| Est. Completion | 2003-11 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00835042
The ClinicalTrials.gov registry entry for NCT00835042 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Teva Pharmaceuticals USA, which has 83 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Moexipril HCl/hydrochlorothiazide 15/25 mg tablets is the first listed.
NCT00835042 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00835042 about?
NCT00835042 is a clinical study titled "Moexipril HCL/Hydrochlorothiazide 15/25 mg Tablets Under Fasting Conditions". The objective of this study is to compare the relative bioavailability of Moexipril HCl/hydrochlorothiazide 15/25 mg tablets (manufactured and distributed by TEVA Pharmaceuticals USA) with that of UNIRETIC® 15/25 mg tablets (Schwartz Pharma) in healthy, adult non-smoking subjects under fasting condi...
What is the current status of trial NCT00835042?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 60 participants. The study started on 2003-10. Estimated completion is 2003-11.
What interventions are being tested in trial NCT00835042?
The interventions under investigation include: Moexipril HCl/hydrochlorothiazide 15/25 mg tablets (DRUG), UNIRETIC® 15/25 mg tablets (DRUG).
Who is sponsoring clinical trial NCT00835042?
This trial is sponsored by Teva Pharmaceuticals USA, which has 83 total clinical trials registered on ClinicalTrials.gov.
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