NCT00866047 · OUTCOME
Duration of Objective Response by Kaplan-Meier Analysis
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
- up to approximately 3 years
What was measured
Duration of objective response (CR + PR) by independent review group, defined as time of initial response until disease progression or death.
Analysis population: Participants with objective response among the intention to treat population
Groups in this outcome
Brentuximab Vedotin
Brentuximab vedotin 1.8 mg/kg every 3 weeks by IV infusion
| Group | Source count |
|---|---|
| Brentuximab Vedotin | 50 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Brentuximab Vedotin | 13.2 | Not reported | 5.7 | 26.3 | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- lower Limit
- 5.7
- upper Limit
- 26.3
- value
- 13.2
- denoms
- counts
- group Id
- OG000
- value
- 50
- units
- Participants
- description
- Duration of objective response (CR + PR) by independent review group, defined as time of initial response until disease progression or death.
- dispersion Type
- 95% Confidence Interval
- groups
- description
- Brentuximab vedotin 1.8 mg/kg every 3 weeks by IV infusion
- id
- OG000
- title
- Brentuximab Vedotin
- param Type
- MEDIAN
- population Description
- Participants with objective response among the intention to treat population
- reporting Status
- POSTED
- time Frame
- up to approximately 3 years
- title
- Duration of Objective Response by Kaplan-Meier Analysis
- type
- SECONDARY
- unit Of Measure
- months
Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0
Preserved source evidence · Independent clinical review pending · Not medical advice
Triangle