Many human cancers depend on deregulated expression of MYC family members for growth and proliferation. Deregulated MYC is transcriptionally regulated by 'super-enhancers' (clusters of enhancers that are occupied densely by transcription factors, cofactors and chromatin regulators). Here, the authors report that a covalent inhibitor of cyclin dependent kinase 7 (CDK7), THZ1, disrupts the transcription of amplified MYCN in neuroblastoma cells and induces tumour regression in a mouse model of neuroblastoma. The selectivity of THZ1 for MYCN-amplified cells correlates with reduced expression of super-enhancer-associated oncogenic drivers, including MYCN.