NCT03762018 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Atezolizumab 1200mg intravenously on day 1 every 3 weeks plus bevacizumab 15mg/kg intravenously on day 1 every 3 weeks plus 4-6 cycles of carboplatin AUC 5 plus pemetrexed 500mg/m\^2 intravenously on day 1 every 3 weeks
- id
- FG000
- title
- Atezolizumab Plus Bevacizumab Plus Chemotherapy
- description
- Bevacizumab 15mg/kg intravenously on day 1 every 3 weeks plus 4-6 cycles of carboplatin AUC 5 plus pemetrexed 500mg/m\^2 intravenously on day 1 every 3 weeks
- id
- FG001
- title
- Bevacizumab Plus Chemotherapy
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 145
- group Id
- FG001
- num Subjects
- 150
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 4
- group Id
- FG001
- num Subjects
- 2
- type
- Withdrawal/Lost to follow-up
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 200
- group Id
- FG001
- num Subjects
- 200
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 198
- comment
- There is one patient assigned in the BC arm who actually received ABC treatment. This patient is evaluated in the treatment arm to which he/she was randomly assigned (BC) for all the efficacy (Intention-to-Treat (ITT)) analyses. For the safety analysis the patient is evaluated according to the treatment he/she received (ABC treatment), irrespective of the allocated treatment at randomization.
- group Id
- FG001
- num Subjects
- 200
- type
- Received at least one dose of trial treatment
- achievements
- group Id
- FG000
- num Subjects
- 8
- group Id
- FG001
- num Subjects
- 4
- comment
- Patients who were on treatment at database cut-off for final efficacy analysis: September 01, 2023
- type
- On treatment
- achievements
- group Id
- FG000
- num Subjects
- 192
- group Id
- FG001
- num Subjects
- 196
- comment
- Atezolizumab plus bevacizumab plus chemotherapy: 109 progressions, 62 toxicities, 9 deaths, 7 investigator decisions, 1 patient decision, 2 other; Bevacizumab plus chemotherapy: 141 progressions, 35 toxicities, 9 deaths, 1 investigator decision, 2 patient decisions, 8 other
- type
- Treatment failures
- achievements
- group Id
- FG000
- num Subjects
- 2
- group Id
- FG001
- num Subjects
- 0
- type
- Never started treatment
- achievements
- group Id
- FG000
- num Subjects
- 51
- group Id
- FG001
- num Subjects
- 48
- comment
- Patients who were on follow-up at database cut-off for final efficacy analysis: September 01, 2023
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 149
- group Id
- FG001
- num Subjects
- 152
- type
- NOT COMPLETED
- title
- Overall Study
Complete source fields
- groups
- description
- Atezolizumab 1200mg intravenously on day 1 every 3 weeks plus bevacizumab 15mg/kg intravenously on day 1 every 3 weeks plus 4-6 cycles of carboplatin AUC 5 plus pemetrexed 500mg/m\^2 intravenously on day 1 every 3 weeks
- id
- FG000
- title
- Atezolizumab Plus Bevacizumab Plus Chemotherapy
- description
- Bevacizumab 15mg/kg intravenously on day 1 every 3 weeks plus 4-6 cycles of carboplatin AUC 5 plus pemetrexed 500mg/m\^2 intravenously on day 1 every 3 weeks
- id
- FG001
- title
- Bevacizumab Plus Chemotherapy
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 145
- group Id
- FG001
- num Subjects
- 150
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 4
- group Id
- FG001
- num Subjects
- 2
- type
- Withdrawal/Lost to follow-up
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 200
- group Id
- FG001
- num Subjects
- 200
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 198
- comment
- There is one patient assigned in the BC arm who actually received ABC treatment. This patient is evaluated in the treatment arm to which he/she was randomly assigned (BC) for all the efficacy (Intention-to-Treat (ITT)) analyses. For the safety analysis the patient is evaluated according to the treatment he/she received (ABC treatment), irrespective of the allocated treatment at randomization.
- group Id
- FG001
- num Subjects
- 200
- type
- Received at least one dose of trial treatment
- achievements
- group Id
- FG000
- num Subjects
- 8
- group Id
- FG001
- num Subjects
- 4
- comment
- Patients who were on treatment at database cut-off for final efficacy analysis: September 01, 2023
- type
- On treatment
- achievements
- group Id
- FG000
- num Subjects
- 192
- group Id
- FG001
- num Subjects
- 196
- comment
- Atezolizumab plus bevacizumab plus chemotherapy: 109 progressions, 62 toxicities, 9 deaths, 7 investigator decisions, 1 patient decision, 2 other; Bevacizumab plus chemotherapy: 141 progressions, 35 toxicities, 9 deaths, 1 investigator decision, 2 patient decisions, 8 other
- type
- Treatment failures
- achievements
- group Id
- FG000
- num Subjects
- 2
- group Id
- FG001
- num Subjects
- 0
- type
- Never started treatment
- achievements
- group Id
- FG000
- num Subjects
- 51
- group Id
- FG001
- num Subjects
- 48
- comment
- Patients who were on follow-up at database cut-off for final efficacy analysis: September 01, 2023
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 149
- group Id
- FG001
- num Subjects
- 152
- type
- NOT COMPLETED
- title
- Overall Study
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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