An Ascending Single-Dose Study of the Safety, Tolerability and Bioeffect of REGN1193
Completed · Phase 1 · Has a placebo group
Conditions studied: Healthy Volunteers
In brief
Study to assess the safety and tolerability of ascending single-doses of REGN1193 in healthy volunteers.
Key facts
- Study ID
- NCT01933763
- Run by
- Regeneron Pharmaceuticals
- People needed
- 56
- Starts
- 2013-08-01
- Expected to finish
- 2015-01-01
- Last updated by the study team
- 2015-03-13
Who can join
Age: 18 and older, up to 45. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Healthy men and women 18 to 45 years of age (inclusive)
- Body mass index 18.0 to 30.0 kg/m\^2 (inclusive)
- Normal standard 12-lead ECG
- Willing and able to comply with clinic visits and study-related procedures
- Provide signed informed consent
- For sexually active men and women of childbearing potential, willingness to utilize adequate contraception and not become pregnant (or have their partner[s] become pregnant) during and for up to 3 months after participation in the study.
You may not qualify if…
- Any clinically significant abnormalities or other characteristics that would preclude the subject from safely enrolling or successfully completing the study
- History of drug or alcohol abuse within a year prior to the screening visit
- Current regular smoking, or a history of smoking greater than ½ pack
- Receipt of an investigational drug within 30 days of screening, or within 5 half-lives of the investigational drug or therapy being studied (whichever is longer)
- 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 may adversely affect the subject's participation in this study
- Known history of human immunodeficiency virus (HIV) antibody; and/or positive hepatitis B surface antigen (HBsAg), and/or positive hepatitis C antibody (HCV) at the screening visit
- Hospitalization for any reason within 60 days of screening
- History or presence of malignancy (including carcinoma in situ) prior to the screening visit
- Any subject who is the investigator or any sub-investigator, research assistant, pharmacist, study coordinator, or other staff directly involved in the conduct of the protocol, or family member of staff involved in the conduct of the protocol
- Pregnant or breast-feeding women
- (The inclusion/ exclusion criteria provided above are not intended to contain all considerations relevant to a subject's potential participation in this clinical trial).
Where it is running
- Study site — Dallas, Texas, United States
Full record on ClinicalTrials.gov
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