Phase 1/2, multicenter, multiple dose clinical study designed to evaluate lonigutamab in subjects with TED.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
31
subcutaneous injection
subcutaneous injection
Clinical Research Site
Jacksonville, Florida, United States
Clinical Research Site
Atlanta, Georgia, United States
Clinical Research Site
Ann Arbor, Michigan, United States
Incidence and characterization of nonserious treatment emergent adverse events (TEAEs)
Safety and Tolerability
Time frame: Day 1 to Day 169
Incidence and characterization of serious treatment emergent adverse events (TEAEs)
Safety and Tolerability
Time frame: Day 1 to Day 169
PK profile of lonigutamab
minimum observed concentration (Cmin)
Time frame: Day 1 to Day 169
PK profile of lonigutamab
Maximum observed concentration (Cmax)
Time frame: Day 1 to Day 169
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Clinical Research Site
East Setauket, New York, United States
Clinical Research Site
New York, New York, United States
Clinical Research Site
Morgantown, West Virginia, United States
Clinical Research Site
Sydney, New South Wales, Australia
Clinical Research Site
Woolloongabba, Queensland, Australia
Clinical Research Site
Adelaide, South Australia, Australia
Clinical Research Site
East Melbourne, Victoria, Australia
...and 1 more locations