NCT01321554 · BASELINE
Baseline characteristics
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- denoms
- counts
- group Id
- BG000
- value
- 261
- group Id
- BG001
- value
- 131
- group Id
- BG002
- value
- 392
- units
- Participants
- groups
- description
- Participants received lenvatinib 24 mg, hard capsule, orally, once daily, until documentation of disease progression (confirmed by IIR), development of unacceptable toxicity, or withdrawal of consent.
- id
- BG000
- title
- Randomization Phase: Lenvatinib 24 mg
- description
- Participants received matching-placebo, hard capsule, orally, once daily until documentation of disease progression (confirmed by IIR), development of unacceptable toxicity, or withdrawal of consent.
- id
- BG001
- title
- Randomization Phase: Placebo
- description
- Total of all reporting groups
- id
- BG002
- title
- Total
- measures
- classes
- categories
- measurements
- group Id
- BG000
- spread
- 10.57
- value
- 62.1
- group Id
- BG001
- spread
- 10.09
- value
- 61.5
- group Id
- BG002
- spread
- 10.40
- value
- 61.9
- dispersion Type
- STANDARD_DEVIATION
- param Type
- GEOMETRIC_MEAN
- title
- Age, Continuous
- unit Of Measure
- years
- classes
- categories
- measurements
- group Id
- BG000
- value
- 136
- group Id
- BG001
- value
- 56
- group Id
- BG002
- value
- 192
- title
- Female
- measurements
- group Id
- BG000
- value
- 125
- group Id
- BG001
- value
- 75
- group Id
- BG002
- value
- 200
- title
- Male
- param Type
- COUNT_OF_PARTICIPANTS
- title
- Sex: Female, Male
- unit Of Measure
- Participants
Complete source fields
- denoms
- counts
- group Id
- BG000
- value
- 261
- group Id
- BG001
- value
- 131
- group Id
- BG002
- value
- 392
- units
- Participants
- groups
- description
- Participants received lenvatinib 24 mg, hard capsule, orally, once daily, until documentation of disease progression (confirmed by IIR), development of unacceptable toxicity, or withdrawal of consent.
- id
- BG000
- title
- Randomization Phase: Lenvatinib 24 mg
- description
- Participants received matching-placebo, hard capsule, orally, once daily until documentation of disease progression (confirmed by IIR), development of unacceptable toxicity, or withdrawal of consent.
- id
- BG001
- title
- Randomization Phase: Placebo
- description
- Total of all reporting groups
- id
- BG002
- title
- Total
- measures
- classes
- categories
- measurements
- group Id
- BG000
- spread
- 10.57
- value
- 62.1
- group Id
- BG001
- spread
- 10.09
- value
- 61.5
- group Id
- BG002
- spread
- 10.40
- value
- 61.9
- dispersion Type
- STANDARD_DEVIATION
- param Type
- GEOMETRIC_MEAN
- title
- Age, Continuous
- unit Of Measure
- years
- classes
- categories
- measurements
- group Id
- BG000
- value
- 136
- group Id
- BG001
- value
- 56
- group Id
- BG002
- value
- 192
- title
- Female
- measurements
- group Id
- BG000
- value
- 125
- group Id
- BG001
- value
- 75
- group Id
- BG002
- value
- 200
- title
- Male
- param Type
- COUNT_OF_PARTICIPANTS
- title
- Sex: Female, Male
- unit Of Measure
- Participants
Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0
Preserved source evidence · Not medical advice
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