ποΈ Verified NIH Record β’ Updated 2026-07-30
A Study to Assess the Pharmacokinetics and Safety of Bimekizumab in Children and Adolescents With Moderate to Severe Hidradenitis Suppurativa (NCT06921850)
A Multicenter, Open-Label Study to Assess The Pharmacokinetics And Safety of Bimekizumab in Pubertal Children And Adolescents With Moderate to Severe Hidradenitis Suppurativa
π΅ Active, Not Recruiting Phase3 π Investigational Drug / Biologic Sponsor: UCB Biopharma SRL
π©Ί Plain-English Summary (8th-Grade Level)
The purpose of the study is to assess the PK of bimekizumab following subcutaneous (sc) administration in study participants with moderate to severe hidradenitis suppurativa (HS)
Who can join: Review the eligibility criteria below.
Location: Hs0006 50175 β Phoenix, Arizona
Age range: 9 Years to 17 Years
π§ͺ Interventions in This Study
π "Do I Qualify?" β 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria β
π All Participating Trial Locations (18 Sites)
- Hs0006 50175 β Phoenix, Arizona
- Hs0006 50708 β Roseville, California
- Hs0006 50684 β Sacramento, California
- Hs0006 50707 β Washington D.C., District of Columbia
- Hs0006 50199 β Miami, Florida
- Hs0006 50712 β Bowling Green, Kentucky
- Hs0006 50178 β Clarkston, Michigan
- Hs0006 50710 β Fort Gratiot, Michigan
- Hs0006 50711 β Troy, Michigan
- Hs0006 50706 β Chapel Hill, North Carolina
- Hs0006 50202 β Fairborn, Ohio
- Hs0006 50201 β Arlington, Texas
- Hs0006 40326 β Berlin,
- Hs0006 40747 β Mainz,
- Hs0006 40625 β Lodz,
- Hs0006 40761 β Warsaw,
- Hs0006 40095 β Wroclaw,
- Hs0006 40845 β Wroclaw,
π° Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA Β§ 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Hidradenitis Suppurativa
- A Study to Assess Disease Activity and Safety of Subcutaneous Lutikizumab (ABT-981) in Adult Participants With Moderate to Severe Hidradenitis Suppurativa Who Have Failed Anti-Tumor Necrosis Factor (TNF) Therapy and Who Are NaΓ―ve to Biologic Therapy β Phoenix, Arizona
- Study to Evaluate the Efficacy and Safety of Ruxolitinib Cream in Participants With Hidradenitis Suppurativa (TRuE-HS1) β Phoenix, Arizona
- Study of Single Doses of SBT777101 in Subjects With Hidradenitis Suppurativa β Boston, Massachusetts
- Study to Evaluate the Efficacy and Safety of Ruxolitinib Cream in Participants With Hidradenitis Suppurativa (TRuE-HS2) β Birmingham, Alabama
- A Phase 3 Study to Assess Efficacy Safety and Tolerability of Remibrutinib in Adult and Adolescent Patients With Moderate to Severe Hidradenitis Suppurativa β Birmingham, Alabama
Explore by condition: All Hidradenitis Suppurativa clinical trials
π‘ How to Participate
- Check the checklist above to see if you may qualify.
- Review the official NIH record below to find the coordinating site.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.