A Study to Evaluate the Pharmacokinetics, Safety and Tolerability of Upadacitinib in Pediatric Participants With Severe Atopic Dermatitis

PHASE1CompletedINTERVENTIONAL
Enrollment

35

Participants

Timeline

Start Date

January 31, 2019

Primary Completion Date

August 29, 2024

Study Completion Date

August 29, 2024

Conditions
Atopic Dermatitis
Interventions
DRUG

Upadacitinib (ABT-494)

Upadacitinib will be administered orally.

Trial Locations (18)

5021

Haukeland University Hospital /ID# 210162, Bergen

19103

Paddington Testing Co., Inc. /ID# 207079, Philadelphia

26506

West Virginia University Hospitals /ID# 206792, Morgantown

45229

Cincinnati Children's Hospital /ID# 207071, Cincinnati

46256

Dawes Fretzin, LLC /ID# 214958, Indianapolis

76011

Arlington Research Center, Inc /ID# 222901, Arlington

90027

Children's Hospital Los Angeles /ID# 206042, Los Angeles

97239

Oregon Medical Research Center /ID# 206226, Portland

92647-6818

Beach Pediatrics /ID# 207834, Huntington Beach

33146-1837

Pediatric Skin Research, LLC /ID# 213468, Coral Gables

33316-1952

Rybear, Inc /ID# 231801, Fort Lauderdale

31904-8946

IACT Health-Columbus /ID# 216370, Columbus

60611-2927

Northwestern University Feinberg School of Medicine /ID# 206224, Chicago

63141-6399

Duplicate_Washington University of St. Louis /ID# 206972, St Louis

87131-0001

University of New Mexico School of Medicine /ID# 206757, Albuquerque

17033-2360

Penn State University and Milton S. Hershey Medical Center /ID# 207096, Hershey

0450

Rikshospitalet OUS HF /ID# 210163, Oslo

00985

Alma M. Cruz Santana, MD-Private practice /ID# 214890, Carolina

Sponsors

Lead Sponsor

All Listed Sponsors
lead

AbbVie

INDUSTRY