NCT00531284 · OUTCOME
Area Under the Plasma Concentration-time Curve From Time Zero to the Last Concentration Measured (AUC0-last) for Carfilzomib
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- GEOMETRIC_MEAN
- Unit
- h*ng/mL
- Interval / dispersion
- Geometric Coefficient of Variation
- Time frame
- Cycle 1, Day 1, predose and at 5 minutes and 15 minutes post start of infusion (for 30-minute infusion groups only), and at the end of infusion, 5, 15, and 30 minutes; and 1, 2, and 4 hours after the end of the infusion.
Analysis population: Safety population with available pharmacokinetic (PK) data. PK analyses were conducted in solid tumor and multiple myeloma groups only and were not conducted for lymphoma or participants enrolled under Amendment 4 (CFX + dexamethasone).
Groups in this outcome
ST: CFZ 20 mg/m² Bolus
Participants with solid tumors received carfilzomib 20 mg/m² administered by bolus intravenous infusion over 2-10 minutes on Cycle 1 Day 1.
ST: CFZ 20 mg/m²
Participants with solid tumors received carfilzomib 20 mg/m² administered by intravenous infusion over 30 minutes on Cycle 1 Day 1.
ST: CFZ 36 mg/m²
Participants with solid tumors received carfilzomib 36 mg/m² administered by intravenous infusion over 30 minutes on Day 1.
ST: CFZ 45 mg/m²
Participants with solid tumors received carfilzomib 45 mg/m² administered by intravenous infusion over 30 minutes on Day 1.
MM: CFZ 20 mg/m²
Participants with multiple myeloma received carfilzomib 20 mg/m² administered by intravenous infusion over 30 minutes on Cycle 1 Day 1.
| Group | Source count |
|---|---|
| ST: CFZ 20 mg/m² Bolus | 30 |
| ST: CFZ 20 mg/m² | 21 |
| ST: CFZ 36 mg/m² | 6 |
| ST: CFZ 45 mg/m² | 6 |
| MM: CFZ 20 mg/m² | 30 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| ST: CFZ 20 mg/m² Bolus | 251 | 92.0 | Not reported | Not reported | Not reported |
| ST: CFZ 20 mg/m² | 346 | 57.4 | Not reported | Not reported | Not reported |
| ST: CFZ 36 mg/m² | 426 | 70.1 | Not reported | Not reported | Not reported |
| ST: CFZ 45 mg/m² | 536 | 150.4 | Not reported | Not reported | Not reported |
| MM: CFZ 20 mg/m² | 269 | 54.3 | Not reported | Not reported | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- spread
- 92.0
- value
- 251
- group Id
- OG001
- spread
- 57.4
- value
- 346
- group Id
- OG002
- spread
- 70.1
- value
- 426
- group Id
- OG003
- spread
- 150.4
- value
- 536
- group Id
- OG004
- spread
- 54.3
- value
- 269
- denoms
- counts
- group Id
- OG000
- value
- 30
- group Id
- OG001
- value
- 21
- group Id
- OG002
- value
- 6
- group Id
- OG003
- value
- 6
- group Id
- OG004
- value
- 30
- units
- Participants
- dispersion Type
- Geometric Coefficient of Variation
- groups
- description
- Participants with solid tumors received carfilzomib 20 mg/m² administered by bolus intravenous infusion over 2-10 minutes on Cycle 1 Day 1.
- id
- OG000
- title
- ST: CFZ 20 mg/m² Bolus
- description
- Participants with solid tumors received carfilzomib 20 mg/m² administered by intravenous infusion over 30 minutes on Cycle 1 Day 1.
- id
- OG001
- title
- ST: CFZ 20 mg/m²
- description
- Participants with solid tumors received carfilzomib 36 mg/m² administered by intravenous infusion over 30 minutes on Day 1.
- id
- OG002
- title
- ST: CFZ 36 mg/m²
- description
- Participants with solid tumors received carfilzomib 45 mg/m² administered by intravenous infusion over 30 minutes on Day 1.
- id
- OG003
- title
- ST: CFZ 45 mg/m²
- description
- Participants with multiple myeloma received carfilzomib 20 mg/m² administered by intravenous infusion over 30 minutes on Cycle 1 Day 1.
- id
- OG004
- title
- MM: CFZ 20 mg/m²
- param Type
- GEOMETRIC_MEAN
- population Description
- Safety population with available pharmacokinetic (PK) data. PK analyses were conducted in solid tumor and multiple myeloma groups only and were not conducted for lymphoma or participants enrolled under Amendment 4 (CFX + dexamethasone).
- reporting Status
- POSTED
- time Frame
- Cycle 1, Day 1, predose and at 5 minutes and 15 minutes post start of infusion (for 30-minute infusion groups only), and at the end of infusion, 5, 15, and 30 minutes; and 1, 2, and 4 hours after the end of the infusion.
- title
- Area Under the Plasma Concentration-time Curve From Time Zero to the Last Concentration Measured (AUC0-last) for Carfilzomib
- type
- SECONDARY
- unit Of Measure
- h*ng/mL
Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0
Preserved source evidence · Not medical advice
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