NCT00622336 · OUTCOME
Time to Progression
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- Not reported
- Unit
- Not reported
- Interval / dispersion
- Not reported
- Time frame
- Up to 70 months
What was measured
Time to progression based on the myeloma response determination criteria developed by Bladé et al 1998 and is defined as the time from registration to the first documented progression. The progressive disease criteria included increasing monoclonal paraprotein levels, bone marrow findings, worsening lytic bone disease, progressively enlarging extramedullary plasmacytomas, or hypercalcemia.
Analysis population: Time to progression not analyzed per the sponsors decision.
Groups in this outcome
Lenalidomide 25mg
Lenalidomide 25mg by mouth (PO) daily on Days 1 to 21 in each 28 day cycle
| Group | Source count |
|---|---|
| Lenalidomide 25mg | 0 |
Reported measurements
No numerical measurement classes were posted for this outcome. Missing is not zero.
Complete source fields
- denoms
- counts
- group Id
- OG000
- value
- 0
- units
- Participants
- description
- Time to progression based on the myeloma response determination criteria developed by Bladé et al 1998 and is defined as the time from registration to the first documented progression. The progressive disease criteria included increasing monoclonal paraprotein levels, bone marrow findings, worsening lytic bone disease, progressively enlarging extramedullary plasmacytomas, or hypercalcemia.
- groups
- description
- Lenalidomide 25mg by mouth (PO) daily on Days 1 to 21 in each 28 day cycle
- id
- OG000
- title
- Lenalidomide 25mg
- population Description
- Time to progression not analyzed per the sponsors decision.
- reporting Status
- POSTED
- time Frame
- Up to 70 months
- title
- Time to Progression
- type
- SECONDARY
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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