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NCT00820885 · ClinicalTrials.gov registry record · Phase 1
A Double-Blind Multi-Dose Tolerability and Pharmacokinetic Study of Teduglutide
A Phase 1 study, sponsored by Shire.
- Completed
- Registry status
- Phase 1
- Development phase
- 95
- Enrollment target
NCT00820885: Completed Phase 1 study, sponsored by Shire.
NCT00820885 is a Phase 1 study that has completed, run by Shire. The registered enrollment target is 95 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (58% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00820885, a Phase 1 study, has completed, sponsored by Shire.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 95 participants
- Enrollment target
Study Summary
The primary objective of the study was to study the safety and tolerability of teduglutide following a once or possibly twice daily subcutaneous injection for eight consecutive days in healthy subjects. A secondary objective was to study the pharmacokinetics of teduglutide following a once or possibly twice daily injection for eight consecutive days in healthy subjects.
Interventions
- DRUG teduglutide
- DRUG tedguglutide
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 95 participants |
| Start Date | 2006-09-06 |
| Est. Completion | 2007-04-23 |
| Phase | Phase 1 |
What the finished NCT00820885 record still lists
NCT00820885 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 95 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (58% higher).
The record links to 0 conditions, and to 2 interventions - of which teduglutide is the first listed.
NCT00820885 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00820885 about?
NCT00820885 is a clinical study titled "A Double-Blind Multi-Dose Tolerability and Pharmacokinetic Study of Teduglutide". The primary objective of the study was to study the safety and tolerability of teduglutide following a once or possibly twice daily subcutaneous injection for eight consecutive days in healthy subjects. A secondary objective was to study the pharmacokinetics of teduglutide following a once or possib...
What is the current status of trial NCT00820885?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 95 participants. The study started on 2006-09-06. Estimated completion is 2007-04-23.
What interventions are being tested in trial NCT00820885?
The interventions under investigation include: teduglutide (DRUG), tedguglutide (DRUG).
Who is sponsoring clinical trial NCT00820885?
This trial is sponsored by Shire, which has 245 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00820885's enrollment target sits among peer trials
95 610th of 2000 higher than 1,386 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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