A Study to Evaluate the Pharmacokinetics, Safety and Tolerability of Upadacitinib in Pediatric Participants With Severe Atopic Dermatitis
Part of paid clinical trials in Huntington Beach, California.
- Sponsor
- AbbVie
- Study ID
- NCT03646604
- Phase
- PHASE1
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 2 Years - 12 Years
- Healthy Volunteers
- Not accepted
Interventions
- Upadacitinib (ABT-494) — DRUGUpadacitinib will be administered orally.
Study Details
The objective of this study is to evaluate the safety, pharmacokinetics and tolerability of multiple doses of upadacitinib in pediatric participants with severe atopic dermatitis and to evaluate palatability of upadacitinib oral solution in pediatric participants.
Key Dates
- Start date
- Jan 31, 2019
- Status verified
- Feb 2025
- Primary completion
- Aug 29, 2024
- Completion
- Aug 29, 2024
Study Design
- Enrollment
- 35 participants (actual)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- Experimental: Part 1; Cohort 1Participants, 6 to \<12 years of age, will receive low dose of upadacitinib.
- Experimental: Part 1; Cohort 2Participants, 6 to \<12 years of age, will receive high dose of upadacitinib.
- Experimental: Part 1; Cohort 3Participants, 2 to \<6 years of age, will receive low dose of upadacitinib.
- Experimental: Part 1; Cohort 4Participants, 2 to \<6 years of age, will receive high dose of upadacitinib.
- Experimental: Part 2Eligible participants who completed Part 1 will receive weight-dependant low dose of upadacitinib.
Primary Outcome Measure
Maximum Plasma Concentration (Cmax) [ Time Frame: Up to 7 days ]
Locations (15)
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