Disease & disorder

rhabdomyosarcoma

MONDO:0005212

A rare aggressive malignant mesenchymal neoplasm arising from skeletal muscle. It usually occurs in children and young adults. Only a small percentage of tumors arise in the skeletal muscle of the extremities. The majority arise in other anatomical sites.

Clinical trials6
Recruiting2
Drug concepts studied2
Synonyms3

Research intelligence

Directly mapped studies only · unique clinical trials

Current registry observations. Phase counts may overlap. Study start dates are not registry registration dates. Investigational interventions are not approved-treatment recommendations.

Medications under investigation

Verified disease and drug mappings that co-occur within the same study; not evidence of effectiveness.

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MONDO disease family

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Recruiting studies by city

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Trial status

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Trial phase

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Study start year

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Investigated drug interventions

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Clinical trials

6 shown
Ivonescimab in the Treatment of Multiple Advanced TumorsNCT06683846 · 2024-11-20
RECRUITING
Familial Investigations of Childhood Cancer PredispositionNCT03050268 · 2017-04-06
RECRUITING
Indo-cyanine Green (ICG) in Paediatric Oncology MISNCT04854018 · 2021-04-30
COMPLETED
PRospective REgistry of Advanced Stage CancER (PREFER) Patients to Assess Prevalence of Actionable Biomarkers and Driver Mutations to Address Disparities in Precision MedicineNCT05697198 · 2021-04-19
COMPLETED
Vemurafenib in Treating Patients With Relapsed or Refractory Advanced Solid Tumors, Non-Hodgkin Lymphoma, or Histiocytic Disorders With BRAF V600 Mutations (A Pediatric MATCH Treatment Trial)NCT03220035 · 2017-11-08
COMPLETED
Stereotactic Body Radiotherapy (SBRT) for Pulmonary Metastases in Ewing Sarcoma, Rhabdomyosarcoma, and Wilms TumorsNCT02581384 · 2017-01-01
TERMINATED

Disease identity and terminology: MONDO. Trial relationships: ClinicalTrials.gov.