Dose-finding Study of QGE031 as add-on Therapy to Evaluate Efficacy and Safety in Patients With CSU
Part of paid clinical trials in Birmingham, Alabama.
- Sponsor
- Novartis Pharmaceuticals
- Study ID
- NCT02477332
- Phase
- PHASE2
- Status
- Completed
Conditions
- Chronic Spontaneous Urticaria
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- QGE031 — BIOLOGICAL
- Omalizumab — BIOLOGICAL
- Placebo — OTHER
Study Details
This is a placebo and active-controlled phase 2b dose-finding study to evaluate efficacy and safety of QGE031 monthly subcutaneous injections as add-on therapy in patients with Chronic Spontaneous Urticaria.
Key Dates
- Start date
- Jul 15, 2015
- Status verified
- Oct 2018
- Primary completion
- Nov 2, 2016
- Completion
- Jun 12, 2017
Study Design
- Enrollment
- 382 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: QGE031 24 mg s.c. q4wligelizumab 24 mg injection subcutaneous every 4 weeks
- Experimental: QGE031 72 mg s.c. q4wligelizumab 72 mg injection subcutaneous every 4 weeks
- Experimental: QGE031 240 mg s.c. q4wligelizumab 240 mg injection subcutaneous every 4 weeks
- Active Comparator: Omalizumab 300 mg s.c. q4womalizumab 300 mg injection subcutaneous every 4 weeks
- Placebo Comparator: Placebo s.c. q4wplacebo injection subcutaneous every 4 weeks
- Experimental: QGE031 120 mg s.c. s.d.ligelizumab 120 mg injection subcutaneous single dose
Primary Outcome Measure
Percentage of Participants With Complete Hives Response (HSS7=0) [ Time Frame: Week 12 ]
Locations (25)
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