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NCT00880750 · ClinicalTrials.gov registry record · Phase 1
Pharmacodynamic Study of Two Lanthanum Carbonate Formulations in Healthy Adults
A Phase 1 study, sponsored by Shire.
- Completed
- Registry status
- Phase 1
- Development phase
- 72
- Enrollment target
NCT00880750: Completed Phase 1 study, sponsored by Shire.
NCT00880750 is a Phase 1 study that has completed, run by Shire. The registered enrollment target is 72 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (20% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00880750, a Phase 1 study, has completed, sponsored by Shire.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 72 participants
- Enrollment target
Study Summary
This study is being conducted to assess any potential differences in the absorption and excretion between two lanthanum carbonate formulations. This study is also being done to assess the safety and tolerability of the two lanthanum carbonate formulations.
Interventions
- DRUG Lanthanum carbonate Granule Formulation
- DRUG Lanthanum carbonate Chewable Tablets (Fosrenol)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 72 participants |
| Start Date | 2009-01-28 |
| Est. Completion | 2009-06-22 |
| Phase | Phase 1 |
What the finished NCT00880750 record still lists
NCT00880750 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 72 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (20% higher).
The record links to 0 conditions, and to 2 interventions - of which Lanthanum carbonate Granule Formulation is the first listed.
NCT00880750 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00880750 about?
NCT00880750 is a clinical study titled "Pharmacodynamic Study of Two Lanthanum Carbonate Formulations in Healthy Adults". This study is being conducted to assess any potential differences in the absorption and excretion between two lanthanum carbonate formulations. This study is also being done to assess the safety and tolerability of the two lanthanum carbonate formulations.
What is the current status of trial NCT00880750?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 72 participants. The study started on 2009-01-28. Estimated completion is 2009-06-22.
What interventions are being tested in trial NCT00880750?
The interventions under investigation include: Lanthanum carbonate Granule Formulation (DRUG), Lanthanum carbonate Chewable Tablets (Fosrenol) (DRUG).
Who is sponsoring clinical trial NCT00880750?
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 NCT00880750's enrollment target sits among peer trials
72 736th of 2000 higher than 1,254 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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