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NCT00621244 · OUTCOME

Percentages of Participants With Histone Acetylation Induction in Peripheral Blood in Arm 1 (MWF Every Week), Group Y

A Study of Oral LBH589 in Adult Patients With Advanced Hematological Malignancies · Source last updated 2021-01-05

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

Measure
NUMBER
Unit
Percentages of participants
Interval / dispersion
Not reported
Time frame
Days 5, 8, end of study (up to 3.5 years)

Analysis population: Full Analysis Set

Groups in this outcome

Arm 1, Group Y (20 mg)

Panobinostat was administered orally, once-a-day, on Monday-Wednesday-Friday (MWF)

Arm 1, Group Y (30 mg)

Panobinostat was administered orally, once-a-day, on Monday-Wednesday-Friday (MWF)

Arm 1, Group Y (40 mg)

Panobinostat was administered orally, once-a-day, on Monday-Wednesday-Friday (MWF)

Arm 1, Group Y (60 mg)

Panobinostat was administered orally, once-a-day, on Monday-Wednesday-Friday (MWF)

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

Analysis denominator · Participants

GroupSource count
Arm 1, Group Y (20 mg)1
Arm 1, Group Y (30 mg)4
Arm 1, Group Y (40 mg)24
Arm 1, Group Y (60 mg)5

Reported measurements

Day 5 (total= 1, 2, 15, 4)
Values in Percentages of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm 1, Group Y (20 mg)100.0Not reportedNot reportedNot reportedNot reported
Arm 1, Group Y (30 mg)100.0Not reportedNot reportedNot reportedNot reported
Arm 1, Group Y (40 mg)66.7Not reportedNot reportedNot reportedNot reported
Arm 1, Group Y (60 mg)75.0Not reportedNot reportedNot reportedNot reported
Day 8 (total = 1, 3, 11, 4)
Values in Percentages of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm 1, Group Y (20 mg)100.0Not reportedNot reportedNot reportedNot reported
Arm 1, Group Y (30 mg)100.0Not reportedNot reportedNot reportedNot reported
Arm 1, Group Y (40 mg)72.7Not reportedNot reportedNot reportedNot reported
Arm 1, Group Y (60 mg)75.0Not reportedNot reportedNot reportedNot reported
End of Study (total=1, 0, 0, 0)
Values in Percentages of participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Arm 1, Group Y (20 mg)0.0Not reportedNot reportedNot reportedNot reported
Arm 1, Group Y (30 mg)NANot reportedNot reportedNot reportedNo patients were analyzed for this arm.
Arm 1, Group Y (40 mg)NANot reportedNot reportedNot reportedNo patients were analyzed for this arm.
Arm 1, Group Y (60 mg)NANot reportedNot reportedNot reportedNo patients were analyzed for this arm.
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        value
        100.0
      2. group Id
        OG001
        value
        100.0
      3. group Id
        OG002
        value
        66.7
      4. group Id
        OG003
        value
        75.0
    title
    Day 5 (total= 1, 2, 15, 4)
  2. categories
    1. measurements
      1. group Id
        OG000
        value
        100.0
      2. group Id
        OG001
        value
        100.0
      3. group Id
        OG002
        value
        72.7
      4. group Id
        OG003
        value
        75.0
    title
    Day 8 (total = 1, 3, 11, 4)
  3. categories
    1. measurements
      1. group Id
        OG000
        value
        0.0
      2. comment
        No patients were analyzed for this arm.
        group Id
        OG001
        value
        NA
      3. comment
        No patients were analyzed for this arm.
        group Id
        OG002
        value
        NA
      4. comment
        No patients were analyzed for this arm.
        group Id
        OG003
        value
        NA
    title
    End of Study (total=1, 0, 0, 0)
denoms
  1. counts
    1. group Id
      OG000
      value
      1
    2. group Id
      OG001
      value
      4
    3. group Id
      OG002
      value
      24
    4. group Id
      OG003
      value
      5
    units
    Participants
groups
  1. description
    Panobinostat was administered orally, once-a-day, on Monday-Wednesday-Friday (MWF)
    id
    OG000
    title
    Arm 1, Group Y (20 mg)
  2. description
    Panobinostat was administered orally, once-a-day, on Monday-Wednesday-Friday (MWF)
    id
    OG001
    title
    Arm 1, Group Y (30 mg)
  3. description
    Panobinostat was administered orally, once-a-day, on Monday-Wednesday-Friday (MWF)
    id
    OG002
    title
    Arm 1, Group Y (40 mg)
  4. description
    Panobinostat was administered orally, once-a-day, on Monday-Wednesday-Friday (MWF)
    id
    OG003
    title
    Arm 1, Group Y (60 mg)
param Type
NUMBER
population Description
Full Analysis Set
reporting Status
POSTED
time Frame
Days 5, 8, end of study (up to 3.5 years)
title
Percentages of Participants With Histone Acetylation Induction in Peripheral Blood in Arm 1 (MWF Every Week), Group Y
type
SECONDARY
unit Of Measure
Percentages of participants

Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f

Preserved source evidence · Not medical advice