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NCT00633048 · ClinicalTrials.gov registry record · Phase 1
Study Evaluating the Safety and Tolerability of NSA-789
A Phase 1 study, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.
- Completed
- Registry status
- Phase 1
- Development phase
- 64
- Enrollment target
NCT00633048 is a Phase 1 study that has completed, run by Wyeth is now a wholly owned subsidiary of Pfizer. The registered enrollment target is 64 participants.
The verdict
NCT00633048, a Phase 1 study, has completed, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 64 participants
- Enrollment target
Study Summary
This is the first time that NSA-789, a new compound being developed for schizophrenia, will be given to humans. Each healthy subject will receive a single dose, except for 8 subjects who will receive 2 doses-- one dose under fasting conditions and one dose after eating food.
Interventions
- DRUG placebo
- DRUG NSA-789
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 64 participants |
| Start Date | 2008-03 |
| Est. Completion | 2008-05 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00633048
The ClinicalTrials.gov registry entry for NCT00633048 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 64 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.
NCT00633048 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00633048 about?
NCT00633048 is a clinical study titled "Study Evaluating the Safety and Tolerability of NSA-789". This is the first time that NSA-789, a new compound being developed for schizophrenia, will be given to humans. Each healthy subject will receive a single dose, except for 8 subjects who will receive 2 doses-- one dose under fasting conditions and one dose after eating food.
What is the current status of trial NCT00633048?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 64 participants. The study started on 2008-03. Estimated completion is 2008-05.
What interventions are being tested in trial NCT00633048?
The interventions under investigation include: placebo (DRUG), NSA-789 (DRUG).
Who is sponsoring clinical trial NCT00633048?
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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