NCT02290431 · OUTCOME
Composite PharmacoKinetics (PK) of Panobinostat and Bortezomib: Tmax
Study of Panobinostat in Combination With Bortezomib and Dexamethasone in Japanese Patients With Relapsed/Refractory Multiple Myeloma · Source last updated 2019-11-18
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- MEDIAN
- Unit
- hour (h)
- Interval / dispersion
- Full Range
- Time frame
- Predose, 0.5h, 1h, 2h, 3h, 4h 8h, 24h, 48h post dose
What was measured
Tmax: The time to reach maximum (peak) plasma concentration. PK sample collection was performed in subjects who agreed to blood samplings for the PK assessments of PAN and BTZ. The order of administration of the 3 study treatment components was 1) PAN, 2) Dex, and 3) BTZ.
Analysis population: PAS: Pharmacokinetic Analysis Set (PAS): The PK analysis set for PAN (PAS-PAN) consisted of all subjects with at least one evaluable PK concentration of PAN. The PK analysis set for BTZ (PAS-BTZ) consisted of all subjects with at least one evaluable PK concentration of BTZ.
Groups in this outcome
LBH589 + Bortezomib + Dexamethasone
Participants were administered LBH589 (panobinostat)in combination with bortezomib and dexamethasone 2 weeks on/1 week off.
Group identifiers and denominators belong to this outcome only. They may differ in another outcome or in safety reporting.
Analysis denominator · Participants
| Group | Source count |
|---|
| LBH589 + Bortezomib + Dexamethasone | 8 |
|---|
Reported measurements
PAN: C1D1
Analysis denominator · Participants
| Group | Source count |
|---|
| LBH589 + Bortezomib + Dexamethasone | 8 |
|---|
Values in hour (h) · Interval/dispersion: Full Range| Group | Value | Spread | Lower | Upper | Comment |
|---|
| LBH589 + Bortezomib + Dexamethasone | 2.00 | Not reported | 1.00 | 4.00 | Not reported |
|---|
PAN: C1D8
Analysis denominator · Participants
| Group | Source count |
|---|
| LBH589 + Bortezomib + Dexamethasone | 7 |
|---|
Values in hour (h) · Interval/dispersion: Full Range| Group | Value | Spread | Lower | Upper | Comment |
|---|
| LBH589 + Bortezomib + Dexamethasone | 2.00 | Not reported | 0.533 | 3.08 | Not reported |
|---|
BJB432: C1D1
Analysis denominator · Participants
| Group | Source count |
|---|
| LBH589 + Bortezomib + Dexamethasone | 8 |
|---|
Values in hour (h) · Interval/dispersion: Full Range| Group | Value | Spread | Lower | Upper | Comment |
|---|
| LBH589 + Bortezomib + Dexamethasone | 24.0 | Not reported | 4.00 | 48.0 | Not reported |
|---|
BJB432: C1D8
Analysis denominator · Participants
| Group | Source count |
|---|
| LBH589 + Bortezomib + Dexamethasone | 7 |
|---|
Values in hour (h) · Interval/dispersion: Full Range| Group | Value | Spread | Lower | Upper | Comment |
|---|
| LBH589 + Bortezomib + Dexamethasone | 24.0 | Not reported | 3.00 | 24.1 | Not reported |
|---|
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- lower Limit
- 1.00
- upper Limit
- 4.00
- value
- 2.00
- title
- PAN: C1D1
- categories
- measurements
- group Id
- OG000
- lower Limit
- 0.533
- upper Limit
- 3.08
- value
- 2.00
- title
- PAN: C1D8
- categories
- measurements
- group Id
- OG000
- lower Limit
- 4.00
- upper Limit
- 48.0
- value
- 24.0
- title
- BJB432: C1D1
- categories
- measurements
- group Id
- OG000
- lower Limit
- 3.00
- upper Limit
- 24.1
- value
- 24.0
- title
- BJB432: C1D8
- description
- Tmax: The time to reach maximum (peak) plasma concentration. PK sample collection was performed in subjects who agreed to blood samplings for the PK assessments of PAN and BTZ. The order of administration of the 3 study treatment components was 1) PAN, 2) Dex, and 3) BTZ.
- dispersion Type
- Full Range
- groups
- description
- Participants were administered LBH589 (panobinostat)in combination with bortezomib and dexamethasone 2 weeks on/1 week off.
- id
- OG000
- title
- LBH589 + Bortezomib + Dexamethasone
- param Type
- MEDIAN
- population Description
- PAS: Pharmacokinetic Analysis Set (PAS): The PK analysis set for PAN (PAS-PAN) consisted of all subjects with at least one evaluable PK concentration of PAN. The PK analysis set for BTZ (PAS-BTZ) consisted of all subjects with at least one evaluable PK concentration of BTZ.
- reporting Status
- POSTED
- time Frame
- Predose, 0.5h, 1h, 2h, 3h, 4h 8h, 24h, 48h post dose
- title
- Composite PharmacoKinetics (PK) of Panobinostat and Bortezomib: Tmax
- type
- SECONDARY
- unit Of Measure
- hour (h)
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice