NCT01055314 · OUTCOME
Feasibility of the Addition of Cixutumumab to Chemotherapy Determined by Patient Enrollment
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- NUMBER
- Unit
- Proportion of Participants
- Interval / dispersion
- 95% Confidence Interval
- Time frame
- From start to week 26 of therapy
What was measured
Proportion of no Grade 3+ cardiac toxicity.
Analysis population: 18 participants were excluded because of ineligibility or insufficient information to assess feasibility.
Groups in this outcome
IMC-A12
IMC-A12 + Multi-agent intensive chemotherapy regimen.
| Group | Source count |
|---|---|
| IMC-A12 | 82 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| IMC-A12 | 0.9390 | Not reported | 0.8872 | 0.9908 | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- lower Limit
- 0.8872
- upper Limit
- 0.9908
- value
- 0.9390
- denoms
- counts
- group Id
- OG000
- value
- 82
- units
- Participants
- description
- Proportion of no Grade 3+ cardiac toxicity.
- dispersion Type
- 95% Confidence Interval
- groups
- description
- IMC-A12 + Multi-agent intensive chemotherapy regimen.
- id
- OG000
- title
- IMC-A12
- param Type
- NUMBER
- population Description
- 18 participants were excluded because of ineligibility or insufficient information to assess feasibility.
- reporting Status
- POSTED
- time Frame
- From start to week 26 of therapy
- title
- Feasibility of the Addition of Cixutumumab to Chemotherapy Determined by Patient Enrollment
- type
- PRIMARY
- unit Of Measure
- Proportion of Participants
Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0
Preserved source evidence · Not medical advice
Triangle