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NCT00722501 · ClinicalTrials.gov registry record · Phase 1
Study Evaluating the Safety and Pharmacokinetics of Ascending Single IV Doses of ERB-257
A Phase 1 study, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.
- Completed
- Registry status
- Phase 1
- Development phase
- 48
- Enrollment target
NCT00722501: Completed Phase 1 study, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.
NCT00722501 is a Phase 1 study that has completed, run by Wyeth is now a wholly owned subsidiary of Pfizer. The registered enrollment target is 48 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (20% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00722501, a Phase 1 study, has completed, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 48 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics of ascending single IV doses of ERB-257 in healthy subjects
Interventions
- OTHER placebo
- DRUG ERB-257
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 48 participants |
| Start Date | 2008-08 |
| Est. Completion | 2008-11 |
| Phase | Phase 1 |
What the finished NCT00722501 record still lists
NCT00722501 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 48 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (20% lower).
The record links to 0 conditions, and to 2 interventions - of which placebo is the first listed.
NCT00722501 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00722501 about?
NCT00722501 is a clinical study titled "Study Evaluating the Safety and Pharmacokinetics of Ascending Single IV Doses of ERB-257". The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics of ascending single IV doses of ERB-257 in healthy subjects
What is the current status of trial NCT00722501?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 48 participants. The study started on 2008-08. Estimated completion is 2008-11.
What interventions are being tested in trial NCT00722501?
The interventions under investigation include: placebo (OTHER), ERB-257 (DRUG).
Who is sponsoring clinical trial NCT00722501?
This trial is sponsored by Wyeth is now a wholly owned subsidiary of Pfizer, which has 167 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00722501's enrollment target sits among peer trials
48 1025th of 2000 higher than 948 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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