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ORIC's enozertinib showed strong results in NSCLC patients with HER2 or EGFR mutations, leading to a selected dose for future trials.
ORIC Pharmaceuticals reported Phase 1b trial results for enozertinib in previously treated NSCLC patients with HER2 exon 20 mutations, showing a 35% objective response rate and 100% disease control rate at 80 mg daily, with mostly mild side effects.
The 80 mg dose was selected for future first-line development based on tolerability and efficacy, while no further development is planned for the HER2 cohort.
A separate analysis showed strong responses in EGFR atypical mutation patients, including high intracranial response rates.
The company will host a conference call on December 6, 2025, to discuss findings.
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El enozertinib de ORIC mostró fuertes resultados en pacientes con NSCLC con mutaciones de HER2 o EGFR, lo que condujo a una dosis seleccionada para ensayos futuros.