SAR231893-LPS15497- "Dupilumab Effect on Sleep in AD Patients"
Part of paid clinical trials in North Little Rock, Arkansas.
- Sponsor
- Sanofi
- Study ID
- NCT04033367
- Phase
- PHASE4
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Dupilumab — DRUGPharmaceutical form: solution for injection Route of administration: subcutaneous
- Placebo — DRUGPharmaceutical form: solution for injection Route of administration: subcutaneous
Study Details
Primary Objective: To evaluate the effect of dupilumab on sleep quality in adult participants with moderate to severe atopic dermatitis (AD). Secondary Objectives: To evaluate the effect of dupilumab on objective and subjective quantitative sleep parameters, AD related outcomes, and daytime consequences of sleep deprivation. To continue to assess the safety and tolerability throughout the study.
Key Dates
- Start date
- Aug 22, 2019
- Status verified
- Sep 2025
- Primary completion
- Oct 6, 2021
- Completion
- Oct 6, 2021
Study Design
- Enrollment
- 188 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Dupilumab/DupilumabParticipants received dupilumab 600 milligrams (mg) (loading dose) injection subcutaneously (SC) on Day 1 followed by dupilumab 300 mg injection SC every 2 weeks (q2w) up to Week 10 in the double-blind (DB) period of 12 weeks. After completion of DB period, participants entered in the open-label extension (OLE) period (Week 12 to 24) and continued to receive dupilumab 300 mg injection SC q2w from Week 12 up to Week 22.
- Placebo Comparator: Placebo/DupilumabParticipants received placebo matching to dupilumab injection SC on Day 1 then followed by placebo injection SC q2w up to Week 10 in the DB period of 12 weeks. After completion of DB period, participants entered in the OLE period (Week 12 to 24) and received dupilumab 600 mg (loading dose) at Week 12 followed by dupilumab 300 mg injection SC q2w up to Week 22.
Primary Outcome Measure
DB Period: Percent Change From Baseline in Sleep Quality Numerical Rating Scale (NRS) at Week 12 [ Time Frame: Baseline, Week 12 ]
Locations (8)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Investigational Site Number :8400012 | North Little Rock | Arkansas | 72117 | - |
| Investigational Site Number :8400002 | Redwood City | California | 94063 | - |
| Investigational Site Number :8400001 | Rolling Hills Estates | California | 90274 | - |
| Investigational Site Number :8400013 | Colorado Springs | Colorado | 80907 | - |
| Investigational Site Number :8400005 | Denver | Colorado | 80230 | - |
| Investigational Site Number :8400003 | Sarasota | Florida | 34239 | - |
| Investigational Site Number :8400007 | Medford | Oregon | 97504 | - |
| Investigational Site Number :8400008 | Charleston | South Carolina | 29407 | - |
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