NCT01732926 · OUTCOME
Overall Survival (OS)
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
- Not reported
What was measured
Overall survival is defined as the interval from randomization to death from any cause.
Analysis population: Due to the early termination of the study, efficacy data were not mature for all participants, and therefore the prespecified analyses were not conducted.
Groups in this outcome
Idelalisib + Bendamustine + Rituximab
Idelalisib 150 mg tablet twice daily + bendamustine intravenously (starting dose of 90 mg/m\^2 for up to 12 infusions) + rituximab intravenously (375 mg/m\^2 on Day 1 for a total of 6 infusions)
Placebo + Bendamustine + Rituximab
Placebo tablet twice daily + bendamustine intravenously (starting dose of 90 mg/m\^2 for up to 12 infusions) + rituximab intravenously (375 mg/m\^2 on Day 1 for a total of 6 infusions)
| Group | Source count |
|---|---|
| Idelalisib + Bendamustine + Rituximab | 0 |
| Placebo + Bendamustine + Rituximab | 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
- group Id
- OG001
- value
- 0
- units
- Participants
- description
- Overall survival is defined as the interval from randomization to death from any cause.
- groups
- description
- Idelalisib 150 mg tablet twice daily + bendamustine intravenously (starting dose of 90 mg/m\^2 for up to 12 infusions) + rituximab intravenously (375 mg/m\^2 on Day 1 for a total of 6 infusions)
- id
- OG000
- title
- Idelalisib + Bendamustine + Rituximab
- description
- Placebo tablet twice daily + bendamustine intravenously (starting dose of 90 mg/m\^2 for up to 12 infusions) + rituximab intravenously (375 mg/m\^2 on Day 1 for a total of 6 infusions)
- id
- OG001
- title
- Placebo + Bendamustine + Rituximab
- population Description
- Due to the early termination of the study, efficacy data were not mature for all participants, and therefore the prespecified analyses were not conducted.
- reporting Status
- POSTED
- title
- Overall Survival (OS)
- type
- SECONDARY
Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0
Preserved source evidence · Not medical advice
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