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NCT01607892 · OUTCOME

Apparent Total Body Clearance, Uncorrected for Fraction Absorbed (Cl/F) of Selinexor

Safety Study of the Selective Inhibitor of Nuclear Export (SINE) KPT-330 in Patients With Advanced Hematological Cancer · Source last updated 2023-01-26

Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.

Measure
GEOMETRIC_MEAN
Unit
Liter per hour per kilogram (L/h/kg)
Interval / dispersion
Geometric Coefficient of Variation
Time frame
0 (pre-dose), 0.5, 1, 2, 4, 8, 24 and 48 hours post-dose on Day 1, 8 of Cycle 1 and Days 15, 16 or 17 of Cycle 2

What was measured

Cl/F was calculated as Dose/AUC0-inf, uncorrected for fraction absorbed, reported normalized by participant body weight (kg).

Analysis population: PK analysis was defined as all participants who received active drug, selinexor, without the co-administration of another chemotherapeutic (i.e., rituximab), and for whom the PK profile for C1D1 could be adequately characterized. Here 'Overall Number of Participants Analyzed' signifies number of participants analyzed for this outcome measure.

Groups in this outcome

Selinexor (3 mg/m^2)

Participants received selinexor dose of 3 mg/m\^2 orally at Cycle 1, on Day 1, 3, 5, 8, 10, 15, 17, 19, 22 and 24 in schedule 1.

Selinexor (6 mg/m^2)

Participants received selinexor dose of 6 mg/m\^2 orally at Cycle 1, on Day 1, 3, 5, 8, 10, 15, 17, 19, 22 and 24 in schedule 1.

Selinexor (12 mg/m^2)

Participants received selinexor dose of 12 mg/m\^2 orally at Cycle 1, on Day 1, 3, 5, 8, 10, 15, 17, 19, 22 and 24 in schedule 1.

Selinexor (16.8 mg/m^2)

Participants received selinexor dose of 16.8 mg/m\^2 orally at Cycle 1, on Day 1, 3, 5, 8, 15, 17, 19, and 22 in schedule 2.

Selinexor (23 mg/m^2)

Participants received selinexor dose of 23 mg/m\^2 orally at Cycle 1, on Day 1 and 2 of each week for a 28-day cycle in schedule 4.

Selinexor (30 mg/m^2)

Participants received selinexor dose of 30 mg/m\^2 orally at Cycle 1, on Day 1, 3, 4, 8, 10, 15 and 17 in schedule 3, 5 and 9.

Selinexor (35 mg/m^2)

Participants received selinexor dose of 35 mg/m\^2 orally at Cycle 1, on Day 1 and 3 in schedule 6.

Selinexor (40 mg/m^2)

Participants received selinexor dose of 40 mg/m\^2 orally at Cycle 1, on Day 1, 3, 8, 10, 15, 17 followed by an 11-day treatment-free interval (Days 18 through 28) in schedule 8 and 11.

Selinexor (46 mg/m^2)

Participants received selinexor dose of 46 mg/m\^2 orally at Cycle 1, on Day 1 once-weekly in schedule 7.

Selinexor (55 mg/m^2)

Participants received selinexor dose of 55 mg/m\^2 orally at Cycle 1, on Day 1, 3, 8, and 10, followed by an 18-day treatment-free interval (Days 11 through 28) in schedule 10.

Selinexor (60 mg/m^2)

Participants received selinexor dose of 60 mg/m\^2 orally at Cycle 1, on Day 1, 3, 8, 10, 15, and 17, followed by an 11-day treatment-free interval (Days 18 through 28) in schedule 11.

Selinexor (70 mg/m^2)

Participants received selinexor dose of 70 mg/m\^2 orally at Cycle 1, on Day 1, 3, 8, 10, 15, and 17, followed by an 11-day treatment-free interval (Days 18 through 28) in schedule 11.

Selinexor (80 mg/m^2)

Participants received selinexor dose of 80 mg/m\^2 orally at Cycle 1, on Day 1, 3, 8, 10, 15, and 17, followed by an 11-day treatment-free interval (Days 18 through 28) in schedule 11.

Group identifiers and denominators belong to this outcome only. They may differ in another outcome or in safety reporting.

Analysis denominator · Participants

GroupSource count
Selinexor (3 mg/m^2)2
Selinexor (6 mg/m^2)2
Selinexor (12 mg/m^2)6
Selinexor (16.8 mg/m^2)12
Selinexor (23 mg/m^2)12
Selinexor (30 mg/m^2)21
Selinexor (35 mg/m^2)13
Selinexor (40 mg/m^2)8
Selinexor (46 mg/m^2)9
Selinexor (55 mg/m^2)7
Selinexor (60 mg/m^2)3
Selinexor (70 mg/m^2)4
Selinexor (80 mg/m^2)1

Reported measurements

Source class 1
Values in Liter per hour per kilogram (L/h/kg) · Interval/dispersion: Geometric Coefficient of Variation
GroupValueSpreadLowerUpperComment
Selinexor (3 mg/m^2)0.19NANot reportedNot reportedGeometric CV was not calculated as data were available for only two participants.
Selinexor (6 mg/m^2)0.21NANot reportedNot reportedGeometric CV was not calculated as data were available for only two participants.
Selinexor (12 mg/m^2)0.2126.6Not reportedNot reportedNot reported
Selinexor (16.8 mg/m^2)0.2222.8Not reportedNot reportedNot reported
Selinexor (23 mg/m^2)0.2054.9Not reportedNot reportedNot reported
Selinexor (30 mg/m^2)0.2125.3Not reportedNot reportedNot reported
Selinexor (35 mg/m^2)0.2225.9Not reportedNot reportedNot reported
Selinexor (40 mg/m^2)0.2326.2Not reportedNot reportedNot reported
Selinexor (46 mg/m^2)0.2212.9Not reportedNot reportedNot reported
Selinexor (55 mg/m^2)0.2024.6Not reportedNot reportedNot reported
Selinexor (60 mg/m^2)0.1927.5Not reportedNot reportedNot reported
Selinexor (70 mg/m^2)0.227.8Not reportedNot reportedNot reported
Selinexor (80 mg/m^2)NANANot reportedNot reportedGeometric mean and CV were not calculated as data were available for only one participant.
Complete source fields
classes
  1. categories
    1. measurements
      1. comment
        Geometric CV was not calculated as data were available for only two participants.
        group Id
        OG000
        spread
        NA
        value
        0.19
      2. comment
        Geometric CV was not calculated as data were available for only two participants.
        group Id
        OG001
        spread
        NA
        value
        0.21
      3. group Id
        OG002
        spread
        26.6
        value
        0.21
      4. group Id
        OG003
        spread
        22.8
        value
        0.22
      5. group Id
        OG004
        spread
        54.9
        value
        0.20
      6. group Id
        OG005
        spread
        25.3
        value
        0.21
      7. group Id
        OG006
        spread
        25.9
        value
        0.22
      8. group Id
        OG007
        spread
        26.2
        value
        0.23
      9. group Id
        OG008
        spread
        12.9
        value
        0.22
      10. group Id
        OG009
        spread
        24.6
        value
        0.20
      11. group Id
        OG010
        spread
        27.5
        value
        0.19
      12. group Id
        OG011
        spread
        7.8
        value
        0.22
denoms
  1. counts
    1. group Id
      OG000
      value
      2
    2. group Id
      OG001
      value
      2
    3. group Id
      OG002
      value
      6
    4. group Id
      OG003
      value
      12
    5. group Id
      OG004
      value
      12
    6. group Id
      OG005
      value
      21
    7. group Id
      OG006
      value
      13
    8. group Id
      OG007
      value
      8
    9. group Id
      OG008
      value
      9
    10. group Id
      OG009
      value
      7
    11. group Id
      OG010
      value
      3
    12. group Id
      OG011
      value
      4
    units
    Participants
description
Cl/F was calculated as Dose/AUC0-inf, uncorrected for fraction absorbed, reported normalized by participant body weight (kg).
dispersion Type
Geometric Coefficient of Variation
groups
  1. description
    Participants received selinexor dose of 3 mg/m\^2 orally at Cycle 1, on Day 1, 3, 5, 8, 10, 15, 17, 19, 22 and 24 in schedule 1.
    id
    OG000
    title
    Selinexor (3 mg/m^2)
  2. description
    Participants received selinexor dose of 6 mg/m\^2 orally at Cycle 1, on Day 1, 3, 5, 8, 10, 15, 17, 19, 22 and 24 in schedule 1.
    id
    OG001
    title
    Selinexor (6 mg/m^2)
  3. description
    Participants received selinexor dose of 12 mg/m\^2 orally at Cycle 1, on Day 1, 3, 5, 8, 10, 15, 17, 19, 22 and 24 in schedule 1.
    id
    OG002
    title
    Selinexor (12 mg/m^2)
  4. description
    Participants received selinexor dose of 16.8 mg/m\^2 orally at Cycle 1, on Day 1, 3, 5, 8, 15, 17, 19, and 22 in schedule 2.
    id
    OG003
    title
    Selinexor (16.8 mg/m^2)
  5. description
    Participants received selinexor dose of 23 mg/m\^2 orally at Cycle 1, on Day 1 and 2 of each week for a 28-day cycle in schedule 4.
    id
    OG004
    title
    Selinexor (23 mg/m^2)
  6. description
    Participants received selinexor dose of 30 mg/m\^2 orally at Cycle 1, on Day 1, 3, 4, 8, 10, 15 and 17 in schedule 3, 5 and 9.
    id
    OG005
    title
    Selinexor (30 mg/m^2)
  7. description
    Participants received selinexor dose of 35 mg/m\^2 orally at Cycle 1, on Day 1 and 3 in schedule 6.
    id
    OG006
    title
    Selinexor (35 mg/m^2)
  8. description
    Participants received selinexor dose of 40 mg/m\^2 orally at Cycle 1, on Day 1, 3, 8, 10, 15, 17 followed by an 11-day treatment-free interval (Days 18 through 28) in schedule 8 and 11.
    id
    OG007
    title
    Selinexor (40 mg/m^2)
  9. description
    Participants received selinexor dose of 46 mg/m\^2 orally at Cycle 1, on Day 1 once-weekly in schedule 7.
    id
    OG008
    title
    Selinexor (46 mg/m^2)
  10. description
    Participants received selinexor dose of 55 mg/m\^2 orally at Cycle 1, on Day 1, 3, 8, and 10, followed by an 18-day treatment-free interval (Days 11 through 28) in schedule 10.
    id
    OG009
    title
    Selinexor (55 mg/m^2)
  11. description
    Participants received selinexor dose of 60 mg/m\^2 orally at Cycle 1, on Day 1, 3, 8, 10, 15, and 17, followed by an 11-day treatment-free interval (Days 18 through 28) in schedule 11.
    id
    OG010
    title
    Selinexor (60 mg/m^2)
  12. description
    Participants received selinexor dose of 70 mg/m\^2 orally at Cycle 1, on Day 1, 3, 8, 10, 15, and 17, followed by an 11-day treatment-free interval (Days 18 through 28) in schedule 11.
    id
    OG011
    title
    Selinexor (70 mg/m^2)
param Type
GEOMETRIC_MEAN
population Description
PK analysis was defined as all participants who received active drug, selinexor, without the co-administration of another chemotherapeutic (i.e., rituximab), and for whom the PK profile for C1D1 could be adequately characterized. Here 'Overall Number of Participants Analyzed' signifies number of participants analyzed for this outcome measure.
reporting Status
POSTED
time Frame
0 (pre-dose), 0.5, 1, 2, 4, 8, 24 and 48 hours post-dose on Day 1, 8 of Cycle 1 and Days 15, 16 or 17 of Cycle 2
title
Apparent Total Body Clearance, Uncorrected for Fraction Absorbed (Cl/F) of Selinexor
type
SECONDARY
unit Of Measure
Liter per hour per kilogram (L/h/kg)

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Preserved source evidence · Not medical advice