← Eichor
Study identifier: NCT04943198 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Optimization of the Time and Dosage of Vemurafenib in BRAF Positive Juvenile Patients With Refractory Histiocytosis

Condition: Histiocytosis  ·  Sponsor: Anna Raciborska

PhasePhase 2
Planned participants25
Who can joinAll sexes, 1 Year to 18 Years
Healthy volunteersNo

About this study

Prospective, interventional, open, randomized, single-center, non-commercial clinical trial to optimize treatment and dosage of vemurafenib in juvenile patients with histiocytosis resistant to conventional therapy and in whom the BRAF gene mutation has been found.

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

Talk to the study team

Katarzyna Maleszewska  ·  +48 22 32 77 205  ·  klinika.onkologii@imid.med.pl

Always discuss trial participation with your own doctor first.

Locations (1)

Mother and Child InstituteWarsaw, Mazovian, PolandRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT04943198