NCT01015027CompletedPhase 1
A Randomized, Double-Blind, Placebo-Controlled, Single Ascending Dose Phase 1 Study of the Safety and Tolerability of Intravenously Administered REGN668 in Healthy Volunteers
Regeneron Pharmaceuticals1 site in 1 country48 target enrollmentStarted: October 1, 2009Last updated:
Conditions
Interventions
Trial Snapshot
- Phase
- Phase 1
- Status
- Completed
- Sponsor
- Regeneron Pharmaceuticals
- Enrollment
- 48
- Locations
- 1
- Primary Endpoint
- The primary endpoint in the study is the incidence of treatment-emergent adverse events in subjects treated with REGN668 or placebo, reported from the administration of study drug on day 1 to the completion of the study on day 85/visit 11.
Study Overview
Brief Summary
This study will test the safety and tolerability (how the body reacts to the drug) of REGN668 and placebo (an inactive substance that contains no medicine) in healthy subjects.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Single Group
- Primary Purpose
- Treatment
- Masking
- Double (Participant, Investigator)
Eligibility Criteria
- Ages
- 18 Years to 65 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Male or female 18 to 65 years of age.
- •Weight > 50 kg and < 120 kg.
- •For women of childbearing potential, a negative serum pregnancy test at the screening visit (visit 1) and a negative urine pregnancy test on day -
- •Willingness to refrain from the consumption of alcohol for 24 hours prior to each study visit.
- •For men and women of childbearing potential, willingness to utilize adequate contraception and not become pregnant (or have their partner[s] become pregnant) during the full duration of the study.
- •Willing, committed, and able to return for ALL clinic visits and complete all study-related procedures.
- •Able to read, understand and willing to sign the informed consent form.
Exclusion Criteria
- •Onset of a new exercise routine or major change to a previous exercise routine within 4 weeks prior to screening visit.
- •Pregnant or breast-feeding women.
- •Significant concomitant illness or history of significant illness such as cardiac, renal, neurological, endocrinological, metabolic or lymphatic disease, or any other illness or condition that would adversely affect the subject's participation in this study.
- •Hospitalization for any reason within 60 days of screening (visit 1).
- •Known history of Human Immunodeficiency Virus (HIV), Hepatitis B or Hepatitis C, and/or positive Hepatitis B surface antigen (HBsAg), positive Hepatitis C antibody (HCV).
- •Previous exposure to any therapeutic or investigational biological agent. results.
- •History of alcohol or substance abuse within previous 5 years.
Arms & Interventions
Dose 4
Experimental
(3:1, active:placebo)
Intervention: REGN668 (Biological)
Dose 3
Experimental
(3:1, active:placebo)
Intervention: REGN668 (Biological)
Dose 2
Experimental
(3:1, active:placebo)
Intervention: REGN668 (Biological)
Dose 1
Experimental
(3:1, active:placebo)
Intervention: REGN668 (Biological)
Outcomes
Primary Outcomes
The primary endpoint in the study is the incidence of treatment-emergent adverse events in subjects treated with REGN668 or placebo, reported from the administration of study drug on day 1 to the completion of the study on day 85/visit 11.
Time Frame: 85 days
Secondary Outcomes
- Pharmacokinetics: Serum concentrations of REGN668 over time.(85 days)
Investigators
Study Sites (1)
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