NCT02267603 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Patients receive pembrolizumab IV over 30 minutes on day 1. Treatment repeats every 21 days for up to 24 months in the absence of disease progression\* or unacceptable toxicity. \* NOTE: Patients with confirmed disease progression may continue to receive treatment if they are otherwise clinically stable until there is an increase in tumor burden of 25% or more following initial confirmation of progression. Under exceptional circumstances, and with protocol P.I. and CITN P.I. approval, patients may receive treatment beyond 2 years. Laboratory Biomarker Analysis: Ancillary studies Pembrolizumab: Given IV
- id
- FG000
- title
- Treatment (Pembrolizumab)
- periods
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 50
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 6
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 44
- type
- NOT COMPLETED
- title
- Overall Study
- recruitment Details
- The study was expanded from 24 patients to 50 patients at the request of the pharmaceutical collaborator.
Complete source fields
- groups
- description
- Patients receive pembrolizumab IV over 30 minutes on day 1. Treatment repeats every 21 days for up to 24 months in the absence of disease progression\* or unacceptable toxicity. \* NOTE: Patients with confirmed disease progression may continue to receive treatment if they are otherwise clinically stable until there is an increase in tumor burden of 25% or more following initial confirmation of progression. Under exceptional circumstances, and with protocol P.I. and CITN P.I. approval, patients may receive treatment beyond 2 years. Laboratory Biomarker Analysis: Ancillary studies Pembrolizumab: Given IV
- id
- FG000
- title
- Treatment (Pembrolizumab)
- periods
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 50
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 6
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 44
- type
- NOT COMPLETED
- title
- Overall Study
- recruitment Details
- The study was expanded from 24 patients to 50 patients at the request of the pharmaceutical collaborator.
Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0
Preserved source evidence · Not medical advice
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