NCT02290431 · OUTCOME
Minimal Response Rate (MRR) Per Investigator
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- NUMBER
- Unit
- Percentage of participants
- Interval / dispersion
- Not reported
- Time frame
- after 24 weeks (8 cycles; cycle = 21 days)
What was measured
MRR is based on modified EBMT criteria per investigator assessment
Analysis population: FAS: The FAS comprised of all subjects who took at least one dose of any study treatment component.
Groups in this outcome
LBH589 + Bortezomib + Dexamethasone
Participants were administered LBH589 (panobinostat)in combination with bortezomib and dexamethasone 2 weeks on/1 week off.
| Group | Source count |
|---|---|
| LBH589 + Bortezomib + Dexamethasone | 31 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| LBH589 + Bortezomib + Dexamethasone | 9.7 | Not reported | Not reported | Not reported | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- value
- 9.7
- denoms
- counts
- group Id
- OG000
- value
- 31
- units
- Participants
- description
- MRR is based on modified EBMT criteria per investigator assessment
- groups
- description
- Participants were administered LBH589 (panobinostat)in combination with bortezomib and dexamethasone 2 weeks on/1 week off.
- id
- OG000
- title
- LBH589 + Bortezomib + Dexamethasone
- param Type
- NUMBER
- population Description
- FAS: The FAS comprised of all subjects who took at least one dose of any study treatment component.
- reporting Status
- POSTED
- time Frame
- after 24 weeks (8 cycles; cycle = 21 days)
- title
- Minimal Response Rate (MRR) Per Investigator
- type
- SECONDARY
- unit Of Measure
- Percentage of participants
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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