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Study completion pushed from Jun 14, 2026 to Sep 14, 2026
Eligibility criteria shortened, about 27 words
Secondary endpoints: details revised at 2 of 2 entries
MinorStudy completion date: Jun 14, 2026 to Sep 14, 2026
Secondary endpoints revised (2)
Primary endpoint revised
v19
MinorStudy completion date: Mar 14, 2026 to Jun 14, 2026v18
NotablePrimary completion date: Mar 14, 2024 to Mar 14, 2025
Study completion date: Mar 14, 2025 to Mar 14, 2026
v17
MinorPrimary completion date: Jan 5, 2024 to Mar 14, 2024
Study completion date: Jan 5, 2025 to Mar 14, 2025
v16
Show 14 earlier versionsHide 14 earlier versions
MinorPrimary completion date: Jan 1, 2024 to Jan 5, 2024v15
MinorPrimary completion date changed from estimate of Jan 5, 2025 to Jan 1, 2024v14
NotablePrimary completion date: Jan 5, 2024 to Jan 5, 2025v13
MinorPrimary completion date: Nov 3, 2023 to Jan 5, 2024
Study completion date: Nov 3, 2023 to Jan 5, 2025
v12
MinorPrimary and study completion dates: Sep 3, 2023 to Nov 3, 2023v11
NotableEnrollment target: estimated 152 to confirmed 9
Trial status: Recruiting to Active, Not Recruiting
Site details revised
v10
NotablePrimary completion date: Sep 3, 2022 to Sep 3, 2023
Start date: Feb 13, 2020 to Aug 13, 2020
v9
MinorCollaborators shortened, about 4 wordsv8
MinorEligibility criteria expanded, about 53 words
Study description expanded, about 2 words
v7
NotableTrial status: Not Yet Recruiting to Recruiting
Start date changed from estimate of Mar 30, 2020 to Feb 13, 2020
Site details revised
v6
NotableStart date: Dec 30, 2019 to Mar 30, 2020v5
NotableStart date: Nov 3, 2019 to Dec 30, 2019v4
NotableStart date: Sep 3, 2019 to Nov 3, 2019v3
MinorRe-verified, no change to tracked fieldsv2
MinorStudy First Submitted
Stopped: an ongoing trial was terminated, suspended or withdrawn.
Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This phase II trial studies how well pembrolizumab given every 12 weeks works compared to every 3 weeks in treating patients with non-small cell lung cancer. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Giving pembrolizumab every 12 weeks may provide similar disease control with fewer treatments for patients with non-small cell lung cancer when compared to every 3 weeks. Demonstrating that 12 week dosing is as effective as 3 week dosing may also have a significant impact when considering the cost required for these medications.