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OpenTrials
Completed

NCT Number: NCT01209793

Safety and Tolerability Study of REGN846 (SAR302352) in Healthy Volunteers

This study is being conducted to assess the safety and tolerability of a single ascending intravenous (IV) dose of REGN846 in healthy volunteers.

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Key information

Conditions

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Nucleus Network

Melbourne, Australia

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy men and women between the ages of 18 and 65; women must be postmenopausal or surgically sterile
  • Body Mass Index (BMI) between 18.0 and 30.0 kg/m2, inclusive
  • Normal vital signs after resting in a sitting position for 5 minutes:
  • Normal standard 12-lead ECG
  • Willing and able to comply with clinic visits and study-related procedures
  • Provide signed informed consent
  • Able to understand and complete study-related questionnaires

Exclusion criteria

  • Current or prior history of smoking
  • Any illness or condition that would adversely affect the subject's participation in this study
  • Hospitalization within 60 days of the screening visit
  • Any clinically significant abnormalities observed during the screening visit
  • History of or positive human immunodeficiency virus (HIV) screen result at the screening visit
  • History of positive blood test for hepatitis B/hepatitis C or positive hepatitis screen result at the screening visit
  • History of positive drug screen result for drug or alcohol abuse within a year prior to the screening visit
  • Known sensitivity to any of the components of the Investigational Product formulation
  • Participation in any clinical research study evaluating another investigational drug or therapy within 30 days or at least 5 half-lives (whichever is longer), of the investigational drug prior to the screening visit
  • Any condition that would place the subject at risk, interfere with participation in the study
  • History of a parasitic infection or recent (within the previous 6 months) travel to a parasitic endemic area
  • Live/attenuated vaccinations within 12 weeks of screening or during the study
  • Any subjects with planned elective surgery
  • Sexually active men who are unwilling to utilize adequate contraception

Treatment and study plan

REGN846

Biological

5 IV cohorts (Dose 1, 2, 3, 4, 5)

Primary outcomes

  1. Incidence and severity of adverse events

    Time frame: Baseline through end of study

Secondary outcomes

  1. PK profile

    Time frame: Baseline through end of study

  2. Immunogenicity

    Time frame: Visits 2, 8, 10 and 12

Sponsors and collaborators

Lead sponsor

Regeneron Pharmaceuticals

Industry

Collaborators

  • Sanofi

Registry information

Official study title

A Randomized, Double-blind, Placebo-controlled, Single Ascending Dose Study of the Safety and Tolerability of Intravenously Administered REGN846 (SAR302352) in Healthy Volunteers

Important dates

Study start
2010
Primary completion
2011
Study completion
2011
First posted
Sep 27, 2010
Registry last updated
Jun 1, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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