Small molecule · Inhibitor of EGFR and HER2 (ERBB2) · developed by ORIC Pharmaceuticals
Enozertinib is an orally bioavailable, CNS-penetrating covalent inhibitor of mutant EGFR and HER2, particularly exon 20 insertion mutations. It irreversibly binds to and inhibits EGFR/HER2-mediated signaling, inducing cell death in overexpressing tumor cells and potentially targeting CNS primary tumors and metastases.
Summary written with AI from the sources listed at the end of this page.
| Trial | Phase | Condition | Status | Sponsor |
|---|---|---|---|---|
| NCT05315700 | Phase 1/2 | Solid Tumors | Recruiting | ORIC |
Trials of the companies BioRadar tracks, from ClinicalTrials.gov, most advanced phase first.
Solid Tumors
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