NCT03599713 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Participants with recurrent, advanced locoregional disease or distant metastatic disease who did not receive any prior chemotherapy received retifanlimab 500 milligrams (mg), administered by intravenous (IV) infusion over 60 minutes on Day 1 of each 28-day cycle (Q4W).
- id
- FG000
- title
- Chemotherapy: Naïve
- description
- Participants with disease not responding to prior chemotherapy received retifanlimab 500 mg, administered by IV infusion over 60 minutes on Day 1 Q4W.
- id
- FG001
- title
- Chemotherapy: Refractory
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 38
- group Id
- FG001
- num Subjects
- 3
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 17
- group Id
- FG001
- num Subjects
- 0
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 4
- group Id
- FG001
- num Subjects
- 0
- type
- Lost to Follow-up
- reasons
- group Id
- FG000
- num Subjects
- 42
- group Id
- FG001
- num Subjects
- 3
- type
- Discontinued Due to End of Study
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 101
- group Id
- FG001
- num Subjects
- 6
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 101
- group Id
- FG001
- num Subjects
- 6
- type
- Safety Evaluable Population
- achievements
- group Id
- FG000
- num Subjects
- 101
- group Id
- FG001
- num Subjects
- 6
- type
- Enrolled Population
- achievements
- group Id
- FG000
- num Subjects
- 65
- group Id
- FG001
- num Subjects
- 6
- type
- Full Analysis Set
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 101
- group Id
- FG001
- num Subjects
- 6
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- Participants were enrolled and treated at 34 study centers in Italy, France, the United States, Poland, Canada, Switzerland, Hungary, the Czech Republic, Germany, Spain, and the United Kingdom.
Complete source fields
- groups
- description
- Participants with recurrent, advanced locoregional disease or distant metastatic disease who did not receive any prior chemotherapy received retifanlimab 500 milligrams (mg), administered by intravenous (IV) infusion over 60 minutes on Day 1 of each 28-day cycle (Q4W).
- id
- FG000
- title
- Chemotherapy: Naïve
- description
- Participants with disease not responding to prior chemotherapy received retifanlimab 500 mg, administered by IV infusion over 60 minutes on Day 1 Q4W.
- id
- FG001
- title
- Chemotherapy: Refractory
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 38
- group Id
- FG001
- num Subjects
- 3
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 17
- group Id
- FG001
- num Subjects
- 0
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 4
- group Id
- FG001
- num Subjects
- 0
- type
- Lost to Follow-up
- reasons
- group Id
- FG000
- num Subjects
- 42
- group Id
- FG001
- num Subjects
- 3
- type
- Discontinued Due to End of Study
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 101
- group Id
- FG001
- num Subjects
- 6
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 101
- group Id
- FG001
- num Subjects
- 6
- type
- Safety Evaluable Population
- achievements
- group Id
- FG000
- num Subjects
- 101
- group Id
- FG001
- num Subjects
- 6
- type
- Enrolled Population
- achievements
- group Id
- FG000
- num Subjects
- 65
- group Id
- FG001
- num Subjects
- 6
- type
- Full Analysis Set
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 101
- group Id
- FG001
- num Subjects
- 6
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- Participants were enrolled and treated at 34 study centers in Italy, France, the United States, Poland, Canada, Switzerland, Hungary, the Czech Republic, Germany, Spain, and the United Kingdom.
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Preserved source evidence · Not medical advice
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