Clinical trials

4

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Optimization of the Time and Dosage of Trametinib in BRAF Negative Juvenile Patients

Prospective, interventional, open, randomized, single-center, non-commercial clinical trial to optimize treatment and dosage of trametinib in juvenile patients with histiocytosis resistant to conventional therapy and without the BRAF gene mutation or after the failure of vemurafenib treatment.

Participants needed: 12
Trial details
Phase: Phase 2Age: 1-18Biological sex: AllType: InterventionalSponsor: Anna RaciborskaUpdated: Mar 27, 2026Locations: 1
Eligibility criteria

Lack of mutations in the BRAF gene in tumor tissues and/or circulating tumor DNA... [+5]

Lack of inclusion criteria. [+7]

Status: Recruiting

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

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.

Participants needed: 25
Trial details
Phase: Phase 2Age: 1-18Biological sex: AllType: InterventionalSponsor: Anna RaciborskaUpdated: Mar 27, 2026Locations: 1
Eligibility criteria

The presence of mutations in the BRAF gene in tumor tissues and/or in circulatin... [+8]

Lack of inclusion criteria. [+7]

Status: Recruiting

Determination of Molecular Status, the Efficacy and Safety of Fluorodeoxyglucose in PET-CT Imaging

Prospective, low intervention, open, single-center, non-commercial clinical trial to improve diagnostics in patients with histiocytosis by assessing the molecular profile of the tumor tissues, monitoring its presence in free-circulating DNA, and determining the efficacy of fluorodeoxyglucose (18F-FDG) in PET-CT imaging.

Participants needed: 150
Trial details
Phase: Phase 3Age: 1-18Biological sex: AllType: InterventionalSponsor: Anna RaciborskaUpdated: Mar 25, 2026Locations: 1
Eligibility criteria

Patient under 18 years of age at the time of inclusion. [+2]

Lack of inclusion criteria. [+2]

Status: Recruiting

To Evaluate the Efficacy and Safety of Naxitamab in Patients With Refractory Ewing's Sarcoma (Butterfly)

Prospective, interventional, open, randomized, national, multicenter, non-commercial trial

Participants needed: 24
Trial details
Phase: Phase 2Age: 2-21Biological sex: AllType: InterventionalSponsor: Anna RaciborskaUpdated: Apr 10, 2025Locations: 2
Eligibility criteria

Histologically proven Ewing sarcoma of the bone or soft tissues. [+9]

Failure to meet any of the inclusion criteria. [+12]