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ependymoblastoma - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

ependymoblastoma

MONDO:0016715

Also known as:ETMR, C19MC-alteredembryonal tumor with Multilayered Rosettesembryonal tumor with Multilayered Rosettes with C19MC amplification

Find Clinical TrialsTrials

Overview

Ependymoblastoma is a rare type of primitive neuroectodermal tumor (PNET) that usually occurs in young children under the age of 2 and is histologically distinguished by the production of ependymoblastic rosettes. It is associated with an aggressive course and a poor prognosis.

Clinical Trials13 registered · 12 recruiting

Diagnosis

Biomarker and diagnostic research for ependymoblastoma has been reported in the published literature.

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

13 clinical trials registered, 12 recruiting. Interventions under study include drug therapy, biologic therapy, other interventions, and procedural interventions. Pipeline includes 1 PHASE2, 9 PHASE1, 1 EARLY_PHASE1. Research is sponsored by a mix of industry and academic institutions.

NCT ID	Title	Phase	Sponsor	Status
[NCT03911388](https://clinicaltrials.gov/study/NCT03911388)

Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 11:53 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:251880

GARD

Genetic and Rare Diseases Info Center

GARD:20720

Questions for Your Care Team

→Are any of the 13 active clinical trials a good fit for my situation?
→Are there specialists or centers of excellence for this condition in my area?
→Is there a patient registry I should consider joining?

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Research Type	Count	% of Total
Laboratory research	63	44%
New treatment approaches	23	16%
Clinical study results	17	12%
Research summaries	12	8%
Testing and diagnosis research	11	8%
Patient case studies	10	7%
Disease patterns and progression	8	6%

ependymoblastoma

Overview

Diagnosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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