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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 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.
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00722501
The ClinicalTrials.gov registry entry for NCT00722501 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 48 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wyeth is now a wholly owned subsidiary of Pfizer, which has 167 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which placebo is the first listed.
NCT00722501 reports 0 study locations.
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.
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