SAD and MAD Study With IV and SC Doses of ARGX-117
- Conditions
- Healthy Volunteers
- Registration Number
- NCT04532125
- Lead Sponsor
- argenx
- Brief Summary
This is a phase 1, first-in-human, double-blinded, randomized, placebo-controlled, escalating single and multiple dose levels trial to evaluate the safety, pharmacokinetics, pharmacodynamics, and immunogenicity of ARGX-117 administered IV and/or SC. Up to 112 healthy, adult male and female subjects of non-childbearing potential will be enrolled in this trial.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 110
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SEQUENTIAL
- Primary Outcome Measures
Name Time Method Number of (S)AE Up to 37 weeks (arm 1) and up to 42 weeks (arm 2)
- Secondary Outcome Measures
Name Time Method Level of anti-drug antibodies Up to 37 weeks (arm 1) and up to 42 weeks (arm 2) Immunogenicity against ARGX-117
Total C2 concentration Up to 37 weeks (arm 1) and up to 42 weeks (arm 2) Functional complement activity
Area Under The Curve (AUC) Up to 37 weeks (arm 1) and up to 42 weeks (arm 2) Maximum serum concentrations (Cmax) Up to 37 weeks (arm 1) and up to 42 weeks (arm 2) Maximum observed serum concentration
Time to reach maximum serum concentrations (Tmax) Up to 37 weeks (arm 1) and up to 42 weeks (arm 2) Time calculated to reach Cmax
Free C2 concentration Up to 37 weeks (arm 1) and up to 42 weeks (arm 2) Functional complement activity
CH50 titers Up to 37 weeks (arm 1) and up to 42 weeks (arm 2) Functional complement activity
Related Research Topics
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Trial Locations
- Locations (1)
Investigator Site 1
🇳🇱Groningen, Netherlands
Investigator Site 1🇳🇱Groningen, Netherlands