NCT03477539 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Patients receive daratumumab IV on days 1, 8, 15, and 22 of cycles 1-2, and on days 1 and 15 of cycles 3-4. Treatment repeats every 28 days for up to 4 cycles in the absence of disease progression or unacceptable toxicity. Beginning 8 weeks after completion of daratumumab cycle 2 or 4, patients undergo ASCT. Within 14 days after completion of day 100 visit post-SCT, patients receive daratumumab IV on day 1 and lenalidomide PO daily on days 1-21. Treatment repeats every 28 days for up to 12 cycles in the absence of disease progression or unacceptable toxicity. Patients who are still maintaining response continue to receive daratumumab IV every 3 months in the absence of disease progression or unacceptable toxicity.
- id
- FG000
- title
- Treatment (Daratumumab, ASCT, Lenalidomide)
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 3
- type
- Ineligible
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 49
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 46
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 3
- type
- NOT COMPLETED
- title
- Overall Study
Complete source fields
- groups
- description
- Patients receive daratumumab IV on days 1, 8, 15, and 22 of cycles 1-2, and on days 1 and 15 of cycles 3-4. Treatment repeats every 28 days for up to 4 cycles in the absence of disease progression or unacceptable toxicity. Beginning 8 weeks after completion of daratumumab cycle 2 or 4, patients undergo ASCT. Within 14 days after completion of day 100 visit post-SCT, patients receive daratumumab IV on day 1 and lenalidomide PO daily on days 1-21. Treatment repeats every 28 days for up to 12 cycles in the absence of disease progression or unacceptable toxicity. Patients who are still maintaining response continue to receive daratumumab IV every 3 months in the absence of disease progression or unacceptable toxicity.
- id
- FG000
- title
- Treatment (Daratumumab, ASCT, Lenalidomide)
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 3
- type
- Ineligible
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 49
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 46
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 3
- type
- NOT COMPLETED
- title
- Overall Study
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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