Osimertinib in Treating Participants With Stage I-IIIA EGFR-mutant Non-small Cell Lung Cancer Before Surgery
Part of paid clinical trials in Davis, California.
- Sponsor
- University of California, San Francisco
- Study ID
- NCT03433469
- Phase
- PHASE2
- Status
- Active Not Recruiting
Conditions
- Stage I Non-Small Cell Lung Cancer
- Stage IA Non-Small Cell Lung Cancer
- Stage IB Non-Small Cell Lung Cancer
- Stage II Non-Small Cell Lung Cancer
- Stage IIA Non-Small Cell Lung Cancer
- Stage IIB Non-Small Cell Lung Cancer
- Stage IIIA Non-Small Cell Lung Cancer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Osimertinib — DRUGGiven PO (orally)
- Therapeutic Conventional Surgery — PROCEDUREUndergo surgery
Study Details
This phase II trial studies how well osimertinib works in treating participants with stage I-IIIA Epithelial Growth Factor Receptor (EGFR) -mutant non-small cell lung cancer before surgery. Osimertinib may stop the growth of tumor cells by blocking mutant EGFR signaling in cancer cells.
Key Dates
- Start date
- Jul 31, 2018
- Status verified
- Mar 2026
- Primary completion
- Jan 31, 2023
- Completion
- Sep 30, 2027
Study Design
- Enrollment
- 27 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Treatment (osimertinib)Participants receive 80mg osimertinib orally, once a day (PO QD) on days 1-28. Treatment repeats every 28 days for a minimum of 1 cycle prior to surgery in the absence of disease progression or unacceptable toxicity. Investigators will have the option to give a second cycle of study drug prior to surgery if clinically indicated. Depending on the timing of the final scans, patients may ultimately receive up to two weeks additional therapy with study drug beyond end of cycle 1 (or cycle 2) while awaiting surgery. Patients then undergo surgical resection of their cancer. No treatment with the study drug will be given after surgery.
Primary Outcome Measure
Percentage of Participants With a Major Pathological Response (MPR) [ Time Frame: Up to 1 year ]
Locations (3)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of California, Davis | Davis | California | 95864 | - |
| University of California, San Francisco | San Francisco | California | 94143 | - |
| University of Colorado | Aurora | Colorado | 80045 | - |