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SAD and MAD Study With IV and SC Doses of ARGX-117

Phase 1
Completed
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
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SEQUENTIAL
Primary Outcome Measures
NameTimeMethod
Number of (S)AEUp to 37 weeks (arm 1) and up to 42 weeks (arm 2)
Secondary Outcome Measures
NameTimeMethod
Level of anti-drug antibodiesUp to 37 weeks (arm 1) and up to 42 weeks (arm 2)

Immunogenicity against ARGX-117

Total C2 concentrationUp 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 concentrationUp to 37 weeks (arm 1) and up to 42 weeks (arm 2)

Functional complement activity

CH50 titersUp to 37 weeks (arm 1) and up to 42 weeks (arm 2)

Functional complement activity

Trial Locations

Locations (1)

Investigator Site 1

🇳🇱

Groningen, Netherlands

Investigator Site 1
🇳🇱Groningen, Netherlands

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