The purpose of this study is to assess the Safety and Tolerability of REGN668 (how the body reacts to the drug) compared to placebo (an inert substance) in patients with moderate-to-severe extrinsic Atopic Dermatitis.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
30
Unnamed facility
Los Angeles, California, United States
Unnamed facility
Riverside, California, United States
Unnamed facility
Miami, Florida, United States
Unnamed facility
Chicago, Illinois, United States
The primary endpoint in the study is the incidence of treatment-emergent adverse events (TEAEs) in patients treated with REGN668 or Placebo from baseline through week 12.
Time frame: 12 weeks
The secondary endpoint is to characterize PK profile of study drug REGN668 from baseline through week 12.
Time frame: 12 weeks
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Unnamed facility
Troy, Michigan, United States
Unnamed facility
New York, New York, United States
Unnamed facility
Rochester, New York, United States
Unnamed facility
Portland, Oregon, United States
Unnamed facility
Philadelphia, Pennsylvania, United States
Unnamed facility
Dallas, Texas, United States