NCT02541604 · OUTCOME
Overall Survival (OS)
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- MEDIAN
- Unit
- Months
- Interval / dispersion
- 95% Confidence Interval
- Time frame
- Baseline until death (up to approximately 42 months)
Analysis population: Included safety-evaluable population, defined as patients who received any amount of study drug.
Groups in this outcome
Atezolizumab
Participants received intravenous (IV) infusion of atezolizumab (maximum 1200 milligrams \[mg\]) on Day 1 of each 21-day cycle.
| Group | Source count |
|---|---|
| Atezolizumab | 87 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Atezolizumab | 7.4 | Not reported | 5.3 | 9.6 | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- lower Limit
- 5.3
- upper Limit
- 9.6
- value
- 7.4
- denoms
- counts
- group Id
- OG000
- value
- 87
- units
- Participants
- dispersion Type
- 95% Confidence Interval
- groups
- description
- Participants received intravenous (IV) infusion of atezolizumab (maximum 1200 milligrams \[mg\]) on Day 1 of each 21-day cycle.
- id
- OG000
- title
- Atezolizumab
- param Type
- MEDIAN
- population Description
- Included safety-evaluable population, defined as patients who received any amount of study drug.
- reporting Status
- POSTED
- time Frame
- Baseline until death (up to approximately 42 months)
- title
- Overall Survival (OS)
- type
- SECONDARY
- unit Of Measure
- Months
Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0
Preserved source evidence · Not medical advice
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