About this trial
A phase 1 study to determine the safety, tolerability, PK, PD, and preliminary anti-tumor activity of ascending doses of EPI-326 administered to patients with locally advanced or metastatic HNSCC and to patients with any documented EGFR-mutant locally advanced or metastatic NSCLC.
Eligibility criteria
Qualifiers
Participant has a life expectancy > 12 weeks at Day 1.
Participant has an ECOG performance status of 0-2.
Participant has pathologically confirmed NSCLC or HNSCC.
Participant has locally advanced or metastatic NSCLC or HNSCC.
Disqualifiers
Participant has history of uncontrolled illness.
Participant has symptomatic brain metastases.
Participant has a diagnosis of any secondary malignancy within 3 years prior to enrollment, except for those patients treated with curative intent and no evidence of active disease.
Trial design
Treatments tested in this trial
- EPI-326