NCT03433001 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Participants took ixazomib, lenalidomide, and dexamethasone under conditions of standard medical care in this study. The dosage and administration of ixazomib, lenalidomide, and dexamethasone were not defined by the protocol but according to the package insert of each drug.
- id
- FG000
- title
- Ixazomib + Lenalidomide + Dexamethasone
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 109
- type
- Lack of Efficacy
- reasons
- group Id
- FG000
- num Subjects
- 69
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 10
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 12
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 4
- type
- Lost to Follow-up
- reasons
- group Id
- FG000
- num Subjects
- 25
- type
- Other
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 295
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 66
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 229
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- A total of 295 participants were enrolled and received the study treatment in this study.
- recruitment Details
- Participant s took part in the survey at 101 investigative sites in Japan, from 2 April 2018 to 11 June 2021.
Complete source fields
- groups
- description
- Participants took ixazomib, lenalidomide, and dexamethasone under conditions of standard medical care in this study. The dosage and administration of ixazomib, lenalidomide, and dexamethasone were not defined by the protocol but according to the package insert of each drug.
- id
- FG000
- title
- Ixazomib + Lenalidomide + Dexamethasone
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 109
- type
- Lack of Efficacy
- reasons
- group Id
- FG000
- num Subjects
- 69
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 10
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 12
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 4
- type
- Lost to Follow-up
- reasons
- group Id
- FG000
- num Subjects
- 25
- type
- Other
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 295
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 66
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 229
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- A total of 295 participants were enrolled and received the study treatment in this study.
- recruitment Details
- Participant s took part in the survey at 101 investigative sites in Japan, from 2 April 2018 to 11 June 2021.
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Preserved source evidence · Not medical advice
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