NCT02541604 · OUTCOME
PFS as Determined by the Investigator Using mINRC in Participants With Neuroblastoma
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 first documented occurrence of progressive disease, or death from any cause, whichever occurs first (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
Cohort 3
Participants with neuroblastoma.
| Group | Source count |
|---|---|
| Cohort 3 | 11 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Cohort 3 | 2.6 | Not reported | 1.2 | 4.7 | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- lower Limit
- 1.2
- upper Limit
- 4.7
- value
- 2.6
- denoms
- counts
- group Id
- OG000
- value
- 11
- units
- Participants
- dispersion Type
- 95% Confidence Interval
- groups
- description
- Participants with neuroblastoma.
- id
- OG000
- title
- Cohort 3
- 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 first documented occurrence of progressive disease, or death from any cause, whichever occurs first (up to approximately 42 months)
- title
- PFS as Determined by the Investigator Using mINRC in Participants With Neuroblastoma
- type
- PRIMARY
- unit Of Measure
- Months
Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0
Preserved source evidence · Not medical advice
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