NCT04644237 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Participants randomized to receive trastuzumab deruxtecan 5.4 mg/kg, administered by intravenous infusion every 3 weeks (Q3W).
- id
- FG000
- title
- Trastuzumab Deruxtecan 5.4 mg/kg
- description
- Participants randomized to receive trastuzumab deruxtecan 6.4 mg/kg, administered by intravenous infusion every 3 weeks (Q3W).
- id
- FG001
- title
- Trastuzumab Deruxtecan 6.4 mg/kg
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 4
- group Id
- FG001
- num Subjects
- 2
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 18
- group Id
- FG001
- num Subjects
- 19
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 61
- group Id
- FG001
- num Subjects
- 23
- type
- Progressive Disease
- reasons
- group Id
- FG000
- num Subjects
- 4
- group Id
- FG001
- num Subjects
- 1
- type
- Clinical Progression
- reasons
- group Id
- FG000
- num Subjects
- 4
- group Id
- FG001
- num Subjects
- 2
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 4
- group Id
- FG001
- num Subjects
- 0
- type
- Physician Decision
- reasons
- group Id
- FG000
- num Subjects
- 6
- group Id
- FG001
- num Subjects
- 3
- type
- Other
- reasons
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 0
- type
- Randomized but not Treated
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 102
- group Id
- FG001
- num Subjects
- 50
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 102
- group Id
- FG001
- num Subjects
- 50
- type
- NOT COMPLETED
- title
- Overall Study
- recruitment Details
- A total of 152 participants were enrolled and treated at clinic centers in North America, Europe, and Asia-Pacific.
Complete source fields
- groups
- description
- Participants randomized to receive trastuzumab deruxtecan 5.4 mg/kg, administered by intravenous infusion every 3 weeks (Q3W).
- id
- FG000
- title
- Trastuzumab Deruxtecan 5.4 mg/kg
- description
- Participants randomized to receive trastuzumab deruxtecan 6.4 mg/kg, administered by intravenous infusion every 3 weeks (Q3W).
- id
- FG001
- title
- Trastuzumab Deruxtecan 6.4 mg/kg
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 4
- group Id
- FG001
- num Subjects
- 2
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 18
- group Id
- FG001
- num Subjects
- 19
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 61
- group Id
- FG001
- num Subjects
- 23
- type
- Progressive Disease
- reasons
- group Id
- FG000
- num Subjects
- 4
- group Id
- FG001
- num Subjects
- 1
- type
- Clinical Progression
- reasons
- group Id
- FG000
- num Subjects
- 4
- group Id
- FG001
- num Subjects
- 2
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 4
- group Id
- FG001
- num Subjects
- 0
- type
- Physician Decision
- reasons
- group Id
- FG000
- num Subjects
- 6
- group Id
- FG001
- num Subjects
- 3
- type
- Other
- reasons
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 0
- type
- Randomized but not Treated
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 102
- group Id
- FG001
- num Subjects
- 50
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 102
- group Id
- FG001
- num Subjects
- 50
- type
- NOT COMPLETED
- title
- Overall Study
- recruitment Details
- A total of 152 participants were enrolled and treated at clinic centers in North America, Europe, and Asia-Pacific.
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Preserved source evidence · Not medical advice
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