Study to Assess the Safety and Bioeffect of REGN1033 (SAR391786)



Status:Completed
Conditions:Healthy Studies
Therapuetic Areas:Other
Healthy:No
Age Range:60 - Any
Updated:5/5/2014
Start Date:August 2013
End Date:September 2014
Contact:Clinical Trials Administrator
Email:clinicaltrials@regeneron.com

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This is a study to assess the safety and bioeffect of REGN1033 (SAR391786) in healthy
volunteers.


Inclusion Criteria:

1. Males and postmenopausal females aged 60 years and older with no significant health
issues or clinically significant abnormal laboratory values.

2. Low activity lifestyle

3. Diet and exercise adherence

Exclusion Criteria:

1. Significant concomitant illness such as, but not limited to cardiac, renal,
rheumatologic, gastrointestinal, hematological, skeletal/muscular, neurologic,
psychiatric, endocrine, metabolic or immunological disease.

2. Participation in any clinical trial within 6 months prior to screening.

3. Hospitalization, immobilization, or major surgical procedure requiring general
anesthesia within 6 months prior to screening, or any planned surgical procedures
during the study period.

4. Limb amputation (except for toes) and/or any fracture within 6 months.

The above information is not intended to contain all considerations relevant to a
patient's potential participation in a clinical trial and not all inclusion/ exclusion
criteria are listed.
We found this trial at
5
sites
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St. Louis, MO
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Athens, OH
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Boston, MA
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Gainesville, FL
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Orlando, FL
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