About this trial
The purpose of this study is to evaluate the safety, efficacy and pharmacokinetics (PK) of zipalertinib in participants with locally advanced or metastatic Non-Small Cell Lung Cancer (NSCLC) harboring EGFR ex20ins mutations and other mutations.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Written informed consent.
≥18 years of age (or meets the country's regulatory definition of legal adult age, whichever is greater.
Documented EGFR ex20ins status, as determined by local testing performed at a Clinical Laboratory Improvement Amendments (CLIA) certified (United States [US]) or locally certified laboratory (outside the US).
Progressed on or after systemic therapy with an agent targeting ex20ins, either alone or in combination with standard platinum-based chemotherapy for the treatment of advanced disease. Participants who discontinued previous treatment due to unacceptable toxicity are eligible.
Disqualifiers
Participant is currently receiving an investigational drug in a clinical trial or participating in any other type of medical research judged to be scientifically or medically incompatible with this study.
Participant has received Zipalertinib (TAS6417/CLN081) at any time
CNS radiotherapy (gamma knife radiotherapy is allowed) ≤ 12 weeks, thoracic radiotherapy ≤ 28 days, or other palliative radiation ≤ 14 days prior to the first dose of study
Anticancer immunotherapy ≤28 days prior to the first dose of study treatment
Trial design
Parallel
Treatments tested in this trial
TAS6417
DrugOral tablets
CYP Cocktail
DrugSingle dose of CYP enzyme probe substrates (CYP cocktail) alone prior to the start of zipalertinib dosing and a single dose of CYP cocktail in combination with zipalertinib at steady state.
Transporter Cocktail
DrugSingle dose of transporter probe substrates (Transporter cocktail) alone prior to the start of zipalertinib dosing and a single dose of Transporter cocktail in combination with zipalertinib at steady state.
Treatment groups
8
Treatment groupsSee each treatment group below.
Trial outcomes
Primary outcomes
Cohorts 1-4: Objective Response Rate (ORR)
Dose Optimization Substudy: ORR as Assessed by Blinded Independent Central Review (BICR)
Secondary outcomes
Cohorts 1-4: Number of Participants With Treatment Emergent Adverse Events (TEAEs) Graded According to the National Cancer Institute Common Terminology Criteria for Adverse Events Version 5.0 (CTCAE v5.0)
Cohorts 1-4: Number of Participants with Clinically Significant Changes in Clinical Laboratory Parameters
Cohorts 1-4: Number of Participants with Clinically Significant Changes in Vital Signs
Cohorts 1-4: Number of Participants with Clinically Significant Changes in Electrocardiogram (ECG) Parameters
Sponsors and contacts
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