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NCT00783341 · ClinicalTrials.gov registry record · Phase 1
Study of the Safety, Tolerability, and Pharmacokinetics of GAP-134 Administered Intravenously
A Phase 1 study, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.
- Completed
- Registry status
- Phase 1
- Development phase
- 25
- Enrollment target
NCT00783341 is a Phase 1 study that has completed, run by Wyeth is now a wholly owned subsidiary of Pfizer. The registered enrollment target is 25 participants.
The verdict
NCT00783341, a Phase 1 study, has completed, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 25 participants
- Enrollment target
Study Summary
This study will evaluate the safety, tolerability, and pharmacokinetics (PK) of ascending doses of GAP 134 administered as 6-day continuous IV infusions to healthy subjects.
Interventions
- DRUG placebo
- DRUG GAP-134
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 25 participants |
| Start Date | 2008-11 |
| Est. Completion | 2009-02 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00783341
The ClinicalTrials.gov registry entry for NCT00783341 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 25 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.
NCT00783341 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00783341 about?
NCT00783341 is a clinical study titled "Study of the Safety, Tolerability, and Pharmacokinetics of GAP-134 Administered Intravenously". This study will evaluate the safety, tolerability, and pharmacokinetics (PK) of ascending doses of GAP 134 administered as 6-day continuous IV infusions to healthy subjects.
What is the current status of trial NCT00783341?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 25 participants. The study started on 2008-11. Estimated completion is 2009-02.
What interventions are being tested in trial NCT00783341?
The interventions under investigation include: placebo (DRUG), GAP-134 (DRUG).
Who is sponsoring clinical trial NCT00783341?
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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