Pembrolizumab in Patients With Non-Small Cell Lung Cancer and a Performance Status 2
- Sponsor
- University of Birmingham
- Study ID
- NCT02733159
- Phase
- PHASE2
- Status
- Completed
Conditions
- Carcinoma, Non-Small-Cell Lung
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- pembrolizumab — DRUGanti PD-1
Study Details
This study is to determine that pembrolizumab is safe and tolerable at the selected dose for the treatment of Non-Small Cell Lung Cancer (NSCLC) in patients with a performance status of 2. All patients will receive pembrolizumab.
Key Dates
- Start date
- Jan 4, 2017
- Status verified
- Jan 2025
- Primary completion
- Feb 7, 2023
- Completion
- Feb 5, 2024
Study Design
- Enrollment
- 62 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: PembrolizumabPembrolizumab: 200 mg Q3W, intravenous administration for a maximum of 2 years, or until progression or unacceptable toxicity.
Primary Outcome Measure
Toxicity Rate [ Time Frame: Date of patient registration until 6 months after the administration of the last treatment (a maximum of 2 years treatment and 6 months followup after end of treatment) ]
Related coverage on Hipa.ai
- Pembrolizumab Shows Median 9.8-Month OS in NSCLC with PS 2 PatientsPembrolizumab · Feb 10, 2025 · ClinicalTrials.gov
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