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NCT00856310 · ClinicalTrials.gov registry record · Phase 1
A Single-Dose Study of the Safety and Tolerability of REGN475(SAR164877) in Healthy Subjects
A Phase 1 study, sponsored by Regeneron Pharmaceuticals.
- Completed
- Registry status
- Phase 1
- Development phase
- 56
- Enrollment target
NCT00856310: Completed Phase 1 study, sponsored by Regeneron Pharmaceuticals.
NCT00856310 is a Phase 1 study that has completed, run by Regeneron Pharmaceuticals. The registered enrollment target is 56 participants, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00856310, a Phase 1 study, has completed, sponsored by Regeneron Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 56 participants
- Enrollment target
Study Summary
This is a randomized, double-blind, placebo-controlled single-dose study of the safety and tolerability of intravenously administered REGN475 in healthy volunteers. The primary objective of the study is to assess the safety and tolerability of REGN475. The secondary objectives are to characterize the pharmacokinetic and immunogenicity profiles of REGN475.
Interventions
- BIOLOGICAL REGN475 (SAR164877)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 56 participants |
| Start Date | 2009-02 |
| Est. Completion | 2009-11 |
| Phase | Phase 1 |
What the finished NCT00856310 record still lists
NCT00856310 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 56 participants, a relatively small participant target, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target.
The record links to 0 conditions, and to 1 intervention - of which REGN475 (SAR164877) is the first listed.
NCT00856310 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00856310 about?
NCT00856310 is a clinical study titled "A Single-Dose Study of the Safety and Tolerability of REGN475(SAR164877) in Healthy Subjects". This is a randomized, double-blind, placebo-controlled single-dose study of the safety and tolerability of intravenously administered REGN475 in healthy volunteers. The primary objective of the study is to assess the safety and tolerability of REGN475. The secondary objectives are to characterize th...
What is the current status of trial NCT00856310?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 56 participants. The study started on 2009-02. Estimated completion is 2009-11.
What interventions are being tested in trial NCT00856310?
The interventions under investigation include: REGN475 (SAR164877) (BIOLOGICAL).
Who is sponsoring clinical trial NCT00856310?
This trial is sponsored by Regeneron Pharmaceuticals, which has 280 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00856310's enrollment target sits among peer trials
56 902nd of 2000 higher than 1,083 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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