Congenital/infantile spindle cell rhabdomyosarcoma with VGLL2/NCOA2/CITED2 rearrangements

MONDO:0100060

Congenital/infantile spindle cell rhabdomyosarcoma characterized by the presence of gene fusions involving the VGLL2, SRF, TEAD1, NCOA2, and CITED2 genes.

2538 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by

Showing the 400 most recently updated of 459 trials in this tab.