NCT03106779 · OUTCOME
PK Parameter: Tmax for Asciminib
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- MEDIAN
- Unit
- hour (hr)
- Interval / dispersion
- Full Range
- Time frame
- Week 2 Day 1 at: 0hr (pre-dose), 0.5hr, 1hr, 2hr, 3hr, 4hr, 6hr, 8hr & 12hr post-dose
What was measured
Time to reach maximum (peak) plasma concentration after dose administration (time). Actual sampling times were taken into consideration for the pharmacokinetic analysis.
Analysis population: Pharmacokinetic (PK) analysis set (PAS) included all participants who provided at least one evaluable PK concentration.
Groups in this outcome
Asciminib
Participants randomized to asciminib 40mg BID
| Group | Source count |
|---|---|
| Asciminib | 15 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Asciminib | 1.92 | Not reported | 0.983 | 3.33 | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- lower Limit
- 0.983
- upper Limit
- 3.33
- value
- 1.92
- denoms
- counts
- group Id
- OG000
- value
- 15
- units
- Participants
- description
- Time to reach maximum (peak) plasma concentration after dose administration (time). Actual sampling times were taken into consideration for the pharmacokinetic analysis.
- dispersion Type
- Full Range
- groups
- description
- Participants randomized to asciminib 40mg BID
- id
- OG000
- title
- Asciminib
- param Type
- MEDIAN
- population Description
- Pharmacokinetic (PK) analysis set (PAS) included all participants who provided at least one evaluable PK concentration.
- reporting Status
- POSTED
- time Frame
- Week 2 Day 1 at: 0hr (pre-dose), 0.5hr, 1hr, 2hr, 3hr, 4hr, 6hr, 8hr & 12hr post-dose
- title
- PK Parameter: Tmax for Asciminib
- type
- SECONDARY
- unit Of Measure
- hour (hr)
Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0
Preserved source evidence · Not medical advice
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