NCT01858558 · OUTCOME
Overall Survival (OS)
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- COUNT_OF_PARTICIPANTS
- Unit
- Participants
- Interval / dispersion
- Not reported
- Time frame
- 3 years
What was measured
OS assessed by number of participants alive at the end of follow up period.
Analysis population: This is an analysis by intention-to-treat and only considers transplanted patients randomized to the aMILs arm.
Groups in this outcome
aMIL Arm
Patients receive activated Marrow Infiltrating Lymphocytes (aMIL) aMIL: On day 0, patients will receive auto transplant followed by Tadalafil and aMIL. At day 60, patients will receive Lenalidomide.
| Group | Source count |
|---|---|
| aMIL Arm | 70 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| aMIL Arm | 55 | Not reported | Not reported | Not reported | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- value
- 55
- denoms
- counts
- group Id
- OG000
- value
- 70
- units
- Participants
- description
- OS assessed by number of participants alive at the end of follow up period.
- groups
- description
- Patients receive activated Marrow Infiltrating Lymphocytes (aMIL) aMIL: On day 0, patients will receive auto transplant followed by Tadalafil and aMIL. At day 60, patients will receive Lenalidomide.
- id
- OG000
- title
- aMIL Arm
- param Type
- COUNT_OF_PARTICIPANTS
- population Description
- This is an analysis by intention-to-treat and only considers transplanted patients randomized to the aMILs arm.
- reporting Status
- POSTED
- time Frame
- 3 years
- title
- Overall Survival (OS)
- type
- SECONDARY
- unit Of Measure
- Participants
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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