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NCT00648882 · ClinicalTrials.gov registry record · Phase 1
Fasting Study of Levothyroxine Sodium Tablets 300 mcg to Synthroid® Tablets 300 mcg
A Phase 1 study, sponsored by Mylan Pharmaceuticals.
- Completed
- Registry status
- Phase 1
- Development phase
- 33
- Enrollment target
NCT00648882: Completed Phase 1 study, sponsored by Mylan Pharmaceuticals.
NCT00648882 is a Phase 1 study that has completed, run by Mylan Pharmaceuticals. The registered enrollment target is 33 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (45% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00648882, a Phase 1 study, has completed, sponsored by Mylan Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 33 participants
- Enrollment target
Study Summary
The objective of this study was to investigate the bioequivalence of Mylan's levothyroxine sodium 300 mcg tablets to Abbott's Synthroid® 300 mcg tablets following a single, oral 600 mcg dose (2 × 300 mcg) administered under fasting conditions.
Interventions
- DRUG LEVOTHYROXINE SODIUM TABLETS,
- DRUG SYNTHROID® 300 mcg Tablets
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 33 participants |
| Start Date | 2007-03 |
| Est. Completion | 2007-05 |
| Phase | Phase 1 |
What the finished NCT00648882 record still lists
NCT00648882 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 33 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (45% lower).
The record links to 0 conditions, and to 2 interventions - of which LEVOTHYROXINE SODIUM TABLETS, is the first listed.
NCT00648882 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00648882 about?
NCT00648882 is a clinical study titled "Fasting Study of Levothyroxine Sodium Tablets 300 mcg to Synthroid® Tablets 300 mcg". The objective of this study was to investigate the bioequivalence of Mylan's levothyroxine sodium 300 mcg tablets to Abbott's Synthroid® 300 mcg tablets following a single, oral 600 mcg dose (2 × 300 mcg) administered under fasting conditions.
What is the current status of trial NCT00648882?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 33 participants. The study started on 2007-03. Estimated completion is 2007-05.
What interventions are being tested in trial NCT00648882?
The interventions under investigation include: LEVOTHYROXINE SODIUM TABLETS, (DRUG), SYNTHROID® 300 mcg Tablets (DRUG).
Who is sponsoring clinical trial NCT00648882?
This trial is sponsored by Mylan Pharmaceuticals, which has 146 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00648882's enrollment target sits among peer trials
33 1280th of 2000 higher than 705 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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