NCT05565391 · 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 TCR MM who initiated elranatamab (PF-06863135) following TCR eligibility in study C1071003 (NCT04649359) were included.
- id
- FG000
- title
- Study C1071003 Cohort A
- description
- Participants with RW TCR MM who initiated standard of care treatment following TCR eligibility between 16-Nov-2015 and 31-Mar-2022 identified from COTA database were included.
- id
- FG001
- title
- COTA Cohort
- description
- Participants with RW TCR MM who initiated standard of care treatment following TCR eligibility between 16-Nov-2015 and 31-Mar-2022 identified from Flatiron Health database were included.
- id
- FG002
- title
- Flatiron Health Cohort
- periods
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 123
- group Id
- FG001
- num Subjects
- 233
- group Id
- FG002
- num Subjects
- 152
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 123
- group Id
- FG001
- num Subjects
- 233
- group Id
- FG002
- num Subjects
- 152
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- Index date was defined as the date of initiation of the first regimen after TCR MM eligibility. Only participants with an index date between 16-Nov-2015 and 31-Mar-2022 were selected. Participants were observed from the index date to the earliest of death, or the latest available participants record, whichever occurred first.
- recruitment Details
- This retrospective cohort study included triple-class refractory (TCR) multiple myeloma (MM) participants who initiated elranatamab in study C1071003 (NCT04649359) and 2 cohorts of real-world (RW) TCR MM participants who initiated standard of care (SOC) treatment identified from Flatiron Health and COTA databases as external control arms for Study C1071003.
Complete source fields
- groups
- description
- Participants with TCR MM who initiated elranatamab (PF-06863135) following TCR eligibility in study C1071003 (NCT04649359) were included.
- id
- FG000
- title
- Study C1071003 Cohort A
- description
- Participants with RW TCR MM who initiated standard of care treatment following TCR eligibility between 16-Nov-2015 and 31-Mar-2022 identified from COTA database were included.
- id
- FG001
- title
- COTA Cohort
- description
- Participants with RW TCR MM who initiated standard of care treatment following TCR eligibility between 16-Nov-2015 and 31-Mar-2022 identified from Flatiron Health database were included.
- id
- FG002
- title
- Flatiron Health Cohort
- periods
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 123
- group Id
- FG001
- num Subjects
- 233
- group Id
- FG002
- num Subjects
- 152
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 123
- group Id
- FG001
- num Subjects
- 233
- group Id
- FG002
- num Subjects
- 152
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- Index date was defined as the date of initiation of the first regimen after TCR MM eligibility. Only participants with an index date between 16-Nov-2015 and 31-Mar-2022 were selected. Participants were observed from the index date to the earliest of death, or the latest available participants record, whichever occurred first.
- recruitment Details
- This retrospective cohort study included triple-class refractory (TCR) multiple myeloma (MM) participants who initiated elranatamab in study C1071003 (NCT04649359) and 2 cohorts of real-world (RW) TCR MM participants who initiated standard of care (SOC) treatment identified from Flatiron Health and COTA databases as external control arms for Study C1071003.
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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