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NCT02121080 · ClinicalTrials.gov registry record · Phase 1
Study of the Safety and Tolerability of REGN2222(SAR438584) in Healthy Adult Volunteers
A Phase 1 study of Healthy Volunteers, sponsored by Regeneron Pharmaceuticals.
- Completed
- Registry status
- Phase 1
- Development phase
- 132
- Enrollment target
- 3
- Study locations
NCT02121080 is a Phase 1 study of Healthy Volunteers that has completed, run by Regeneron Pharmaceuticals. The registered enrollment target is 132 participants, below the 481-participant average among 283 other Healthy Volunteers trials with a reported enrollment target (73% lower). The trial reports 3 study locations across 3 states.
The verdict
NCT02121080, a Phase 1 study of Healthy Volunteers, has completed, sponsored by Regeneron Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 132 participants
- Enrollment target
- 3
- Study locations
Study Summary
This is a phase 1, randomized, double-blind, placebo-controlled study evaluating the safety, tolerability, pharmacokinetic (PK) profile, and immunogenicity of REGN2222 ascending in cohorts of healthy adult volunteers.
Conditions Studied
Interventions
- DRUG placebo
- DRUG REGN2222(SAR438584)
Study Locations (3)
Florida
- - Daytona Beach
Indiana
- - Evansville
Texas
- - Dallas
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 132 participants |
| Start Date | 2014-05 |
| Est. Completion | 2015-02 |
| Phase | Phase 1 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02121080
The ClinicalTrials.gov registry entry for NCT02121080 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 132 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 481-participant average among 283 other Healthy Volunteers trials with a reported enrollment target (73% lower). The listed sponsor is Regeneron Pharmaceuticals, which has 280 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Healthy Volunteers appearing as the primary indexed condition, and to 2 interventions - of which placebo is the first listed.
NCT02121080 reports 3 study locations spanning 3 distinct geographic areas - top geographies include Florida, Indiana, Texas.
Frequently Asked Questions
What is clinical trial NCT02121080 about?
NCT02121080 is a clinical study titled "Study of the Safety and Tolerability of REGN2222(SAR438584) in Healthy Adult Volunteers". This is a phase 1, randomized, double-blind, placebo-controlled study evaluating the safety, tolerability, pharmacokinetic (PK) profile, and immunogenicity of REGN2222 ascending in cohorts of healthy adult volunteers.
What is the current status of trial NCT02121080?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 132 participants. The study started on 2014-05. Estimated completion is 2015-02.
What conditions does trial NCT02121080 study?
This clinical trial studies the following conditions: Healthy Volunteers.
What interventions are being tested in trial NCT02121080?
The interventions under investigation include: placebo (DRUG), REGN2222(SAR438584) (DRUG).
Who is sponsoring clinical trial NCT02121080?
This trial is sponsored by Regeneron Pharmaceuticals, which has 280 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02121080 being conducted?
This trial has 3 study locations across Florida, Indiana, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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