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Study identifier: NCT05233397 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

ACTEMRA® for the Treatment of Pediatric Adamantinomatous Craniopharyngioma

Condition: Adamantinomatous Craniopharyngioma · Recurrent Adamantinomatous Craniopharyngioma  ·  Sponsor: Nationwide Children's Hospital

PhasePhase 2
Planned participants30
Who can joinAll sexes, 1 Year to 39 Years
Healthy volunteersNo

About this study

ACTEMRA (tocilizumab) is an IL-6 receptor antagonist used for the treatment of adult Rheumatoid Arthritis as well as Polyarticular (PJIA) and Systemic (SJIA) Juvenile Idiopathic Arthritis. In this Phase II, the drug will be used to treat pediatric patients diagnosed with recurrent Adamantinomatous Craniopharyngioma including patients who have undergone surgery and/or radiation therapy.

This description comes directly from the study's public registry record.

Talk to the study team

Kelsey H Troyer, PhD  ·  16147223284  ·  kelsey.troyer@nationwidechildrens.org

Always discuss trial participation with your own doctor first.

Locations (14)

Children's Hospital ColoradoAurora, Colorado, United StatesRecruiting
Children's National Medical CenterWashington D.C., District of Columbia, United StatesRecruiting
Nicklaus Children's HospitalMiami, Florida, United StatesActive Not Recruiting
Duke Children's HospitalDurham, North Carolina, United StatesRecruiting
Cincinnati Children's Hospital Medical CenterCincinnati, Ohio, United StatesRecruiting
Nationwide Children's HospitalColumbus, Ohio, United StatesRecruiting
Texas Children's HospitalHouston, Texas, United StatesRecruiting
Seattle Children's HospitalSeattle, Washington, United StatesRecruiting
Sydney Children's HospitalRandwick, New South Wales, AustraliaRecruiting
Queensland Children's HospitalSouth Brisbane, Queensland, AustraliaRecruiting
Perth Children's HospitalPerth, Western Australia, AustraliaRecruiting
Stollery Children's HospitalEdmonton, Alberta, CanadaRecruiting

+ 2 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT05233397