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NCT00822835 · ClinicalTrials.gov registry record · Phase 1
Study Evaluating Single Doses of ILV-095 in Healthy Subjects
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
NCT00822835 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
NCT00822835, 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 and tolerability of single doses of ILV-095 in healthy subjects.
Interventions
- BIOLOGICAL Placebo
- BIOLOGICAL ILV-095
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 48 participants |
| Start Date | 2009-01 |
| Est. Completion | 2009-08 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00822835
The ClinicalTrials.gov registry entry for NCT00822835 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.
NCT00822835 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00822835 about?
NCT00822835 is a clinical study titled "Study Evaluating Single Doses of ILV-095 in Healthy Subjects". The purpose of this study is to evaluate the safety and tolerability of single doses of ILV-095 in healthy subjects.
What is the current status of trial NCT00822835?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 48 participants. The study started on 2009-01. Estimated completion is 2009-08.
What interventions are being tested in trial NCT00822835?
The interventions under investigation include: Placebo (BIOLOGICAL), ILV-095 (BIOLOGICAL).
Who is sponsoring clinical trial NCT00822835?
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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Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.