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NCT01484600 · ClinicalTrials.gov registry record · Phase 1
Study of the Safety, Tolerability, Pharmacokinetics, and Immunogenicity of REGN668 Administered Subcutaneously to Healthy Volunteers
A Phase 1 study, sponsored by Regeneron Pharmaceuticals.
- Completed
- Registry status
- Phase 1
- Development phase
- 36
- Enrollment target
NCT01484600: Completed Phase 1 study, sponsored by Regeneron Pharmaceuticals.
NCT01484600 is a Phase 1 study that has completed, run by Regeneron Pharmaceuticals. The registered enrollment target is 36 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (40% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01484600, a Phase 1 study, has completed, sponsored by Regeneron Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 36 participants
- Enrollment target
Study Summary
This is a study of the Safety, Tolerability, Pharmacokinetics, and Immunogenicity of REGN668 Administered Subcutaneously to Healthy Volunteers.
Interventions
- DRUG REGN668: Injection Rate 1
- DRUG REGN668: Injection Rate 2
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 36 participants |
| Start Date | 2011-12 |
| Est. Completion | 2012-02 |
| Phase | Phase 1 |
What the finished NCT01484600 record still lists
NCT01484600 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 36 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (40% lower).
The record links to 0 conditions, and to 2 interventions - of which REGN668: Injection Rate 1 is the first listed.
NCT01484600 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01484600 about?
NCT01484600 is a clinical study titled "Study of the Safety, Tolerability, Pharmacokinetics, and Immunogenicity of REGN668 Administered Subcutaneously to Healthy Volunteers". This is a study of the Safety, Tolerability, Pharmacokinetics, and Immunogenicity of REGN668 Administered Subcutaneously to Healthy Volunteers.
What is the current status of trial NCT01484600?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 36 participants. The study started on 2011-12. Estimated completion is 2012-02.
What interventions are being tested in trial NCT01484600?
The interventions under investigation include: REGN668: Injection Rate 1 (DRUG), REGN668: Injection Rate 2 (DRUG).
Who is sponsoring clinical trial NCT01484600?
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 NCT01484600's enrollment target sits among peer trials
36 1210th of 2000 higher than 743 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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