Overview
Apremilast Pediatric Study in Children With Active Oral Ulcers Associated With Behçet's Disease
Status:
Recruiting
Recruiting
Trial end date:
2029-01-01
2029-01-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The aim of this study is to estimate the efficacy of apremilast compared to placebo in the treatment of oral ulcers in pediatric participants from 2 to < 18 years of age with oral ulcers associated with Behçet's disease (BD) through week 12.Phase:
Phase 3Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
AmgenTreatments:
Apremilast
Criteria
Key Inclusion Criteria- Male or Female participants 2 to < 18 years of age at randomization.
- Diagnosed with behçet's disease (BD) meeting the International Study Group for Behçet
Disease (ISGBD) criteria at any time prior to the screening visit.
- Oral ulcers that occurred ≥ 3 times within the 12-month period prior to the screening
visit.
- Participant must have ≥ 2 oral ulcers at both the screening visit and on day 1.
- Participant has had prior treatment with ≥ 1 non-biologic BD therapy, such as, but not
limited to, topical corticosteroids or systemic treatment.
Key Exclusion Criteria
- Behcet's disease-related active major organ involvement - pulmonary (eg, pulmonary artery
aneurysm), vascular (eg, thrombophlebitis), gastrointestinal (eg, ulcers along the
gastrointestinal tract), and central nervous system (CNS) (eg, meningoencephalitis)
manifestations, and ocular lesions (eg, uveitis) requiring immunosuppressive therapy;
however:
- Previous major organ involvement is allowed if it occurred ≥1 year prior to the
screening visit and is not active at time of enrollment
- Participants with mild BD-related ocular lesions not requiring systemic
immunosuppressive therapy are allowed
- Participants with BD-related arthritis and BD-skin manifestations are also allowed.
- Participants with BD-related arthritis and BD-skin manifestations are also allowed.
Previous exposure to biologic therapies for the treatment of BD oral ulcers, previous
biologic exposure is allowed for other indications (including other manifestations of
BD).