NCT03614728 · OUTCOME
Part 1: Progression Free Survival
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- MEDIAN
- Unit
- Months
- Interval / dispersion
- Inter-Quartile Range
- Time frame
- Up to 30.8 months
What was measured
Progression free survival is defined as time from first dose to disease progression, as defined by IWG criteria, or death due to any cause, whichever occurs earlier. Progressive Disease (PD) is defined as at least a 20% increase in the sum of the diameters of target lesions, taking as reference the smallest sum on study.
Analysis population: All Treated Population.
Groups in this outcome
Part 1: GSK3326595 400 mg
Participants received GSK3326595 400 mg, tablets, orally, once daily until progression, unacceptable toxicity, or withdrawal of consent during Part 1 of the study.
Part 1: GSK3326595 300 mg
Participants received GSK3326595 300 mg, tablets, orally, once daily until progression, unacceptable toxicity, or withdrawal of consent during Part 1 of the study.
| Group | Source count |
|---|---|
| Part 1: GSK3326595 400 mg | 13 |
| Part 1: GSK3326595 300 mg | 17 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Part 1: GSK3326595 400 mg | 0.99 | Not reported | 0.95 | 2.53 | Not reported |
| Part 1: GSK3326595 300 mg | 0.99 | Not reported | 0.95 | 2.43 | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- lower Limit
- 0.95
- upper Limit
- 2.53
- value
- 0.99
- group Id
- OG001
- lower Limit
- 0.95
- upper Limit
- 2.43
- value
- 0.99
- denoms
- counts
- group Id
- OG000
- value
- 13
- group Id
- OG001
- value
- 17
- units
- Participants
- description
- Progression free survival is defined as time from first dose to disease progression, as defined by IWG criteria, or death due to any cause, whichever occurs earlier. Progressive Disease (PD) is defined as at least a 20% increase in the sum of the diameters of target lesions, taking as reference the smallest sum on study.
- dispersion Type
- Inter-Quartile Range
- groups
- description
- Participants received GSK3326595 400 mg, tablets, orally, once daily until progression, unacceptable toxicity, or withdrawal of consent during Part 1 of the study.
- id
- OG000
- title
- Part 1: GSK3326595 400 mg
- description
- Participants received GSK3326595 300 mg, tablets, orally, once daily until progression, unacceptable toxicity, or withdrawal of consent during Part 1 of the study.
- id
- OG001
- title
- Part 1: GSK3326595 300 mg
- param Type
- MEDIAN
- population Description
- All Treated Population.
- reporting Status
- POSTED
- time Frame
- Up to 30.8 months
- title
- Part 1: Progression Free Survival
- type
- SECONDARY
- unit Of Measure
- Months
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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