OncoMatch/Clinical Trials/NCT06046495
A Study of the Oral EGFR Inhibitor PLB1004 in Non-Small Cell Lung Cancer
Is NCT06046495 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies PLB1004 for non-small cell lung cancer.
Treatment: PLB1004 — This is a Phase I, multicenter, open-label, dose escalation and dose expansion study to assess the safety and pharmacokinetic profile of PLB1004, a mono-anilino-pyrimidine compound, given alone in NSCLC patients with EGFR exon 20 insertion mutations,uncommon mutations, classical mutations (Ex19del and L858R), and drug-resistant mutation (T790M). Patients will be enrolled and dosed according to the most current protocol. This study is made of two Parts. Part 1 includes a dose escalation into 7 cohorts and patient allocation to these cohorts will be via slot allocation. Each cohort has a minimum of 3 and a maximum of 6 patients for a total of 21 - 42 patients. The patient population of the dose escalation phase will include patients with advanced NSCLC harboring EGFR classical mutations or Ex20ins mutations, or uncommon mutations. Part 2 includes an expansion phase and the expansion phase will explore one or more dose levels of PLB1004 in NSCLC patients with EGFR Ex20ins mutations, classical mutations, or uncommon mutations.
Check if I qualifyExtracted eligibility criteria
Cancer type
Non-Small Cell Lung Carcinoma
Biomarker criteria
Required: EGFR mutation
Prior therapy
Cannot have received: radiotherapy
Received radiotherapy within 14 days before enrollment
Cannot have received: experimental drugs
Have used other experimental drugs within 2 weeks prior to the first dose of PLB1004
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- University of California-Davis · Sacramento, California
- Research Site · Louisville, Kentucky
- Nebraska Cancer Specialists · Omaha, Nebraska
- Research Site · New York, New York
- Sarah Cannon Research Institute · Nashville, Tennessee
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