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Study identifier: NCT06742073 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Histiocytosis and Inflammatory Manifestations in Patients with H Syndrome

Condition: H Syndrome  ·  Sponsor: Rabin Medical Center

PhaseN/A
Planned participants120
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

H syndrome is a rare genetic disorder predisposing to histiocytosis. Our knowledge of the clinical spectrum of these patients is based on case reports and small patient series. Patients with H syndrome have been treated with a range of immunomodulatory and chemotherapeutic agents, with limited success. We aim to comprehensively assess the clinical manifestations and patterns of treatment response in a multinational cohort of patients with H syndrome.

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

Talk to the study team

Sarah Elitzur, MD  ·  +97239253766  ·  sarhae@clalit.org.il

Naomi Litichever, PhD  ·  +97239253705  ·  naomilitichever@clalit.org.il

Always discuss trial participation with your own doctor first.

Locations (1)

Schneider Children's Medical CenterPetah Tikva, IsraelRecruiting

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Source record: clinicaltrials.gov/study/NCT06742073