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Association details:
Biomarker:EGFRvIII mutation
Cancer:Astrocytoma
Drug:WSD0922 (EGFR inhibitor, EGFRvIII inhibitor)
Direction:Sensitive
Evidence:
Evidence Level:
Sensitive: C3 – Early Trials
Source:
Title:

First-in-human phase 1 trial of the safety, tolerability, pharmacokinetics, and preliminary anti-tumor activity of WSD0922-Fu: Initial report from dose escalation cohort.

Published date:
05/25/2023
Excerpt:
Among patients treated at MTD or higher dose levels and with available response data, 100% (5/5) of patients with NSCLC demonstrated clinical benefit (SD + PR) while 60% of patients had partial responses (intracranial and extracranial)….The MTD for WSD0922-Fu monotherapy is 160 mg BID. Preliminary efficacy was observed in patients with osimertinib-resistant NSCLC and EGFRvIII mutant HGA.
DOI:
10.1200/JCO.2023.41.16_suppl.3109
Trial ID: