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A Study to Investigate the Pharmacokinetics and Safety of Dupilumab in Participants ≥2 Years to <12 Years of Age With Uncontrolled Chronic Spontaneous Urticaria (CSU) (LIBERTY-CSU CUPIDKids)

Completed · Phase 3 · NCT05526521

Conditions: Chronic Spontaneous Urticaria

At a glance

Research payments reported, 2025
$152,580
U.S. investigators named
7
Sites paid
7
Planned or actual enrollment
15

About the trial

Sponsor
Sanofi
Tested
Dupilumab (drug)
Dates
Started 2022-08-25; completion 2025-02-03
Results posted
Yes

This was a multicenter, single-arm, 24-week treatment, Phase 3 study. The purpose of this study was to investigate the PK and safety of dupilumab in children diagnosed with CSU who remain symptomatic despite the use of H1-antihistamine treatment. Study details included: Screening: 2 to 4 weeks; The treatment duration was 24 weeks; Follow-up period: 12 weeks; The study duration was 38 to 40 weeks (including screening and follow-up); The number of study visits was 6.

From ClinicalTrials.gov, last updated 2025-11-25. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Sanofi US Services Inc. reported $152,580 in research payments for this study in 2025 (18 payments).

Products named: Dupixent

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.