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NCT01445080 · OUTCOME

Number of Patients With DEMRI

Sorafenib in Treating Young Patients With Relapsed or Refractory Solid Tumors or Leukemia · Source last updated 2021-02-02

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

Measure
COUNT_OF_PARTICIPANTS
Unit
Participants
Interval / dispersion
Not reported
Time frame
Up to 2 years

What was measured

Assess effect on tumor blood flow via DEMRI in patients with measurable soft tissue tumors.

Analysis population: There were 55 evaluable patients

Groups in this outcome

Part A: Refractory Solid Tumors: BAY 43-9006 105 mg/m^2

Patients receive oral sorafenib 105 mg/m\^2 every 12 hours.

Part A: Refractory Solid Tumors: BAY 43-9006 130 mg/m^2

Patients receive oral sorafenib 130 mg/m\^2 every 12 hours.

Part A: Refractory Solid Tumors: BAY 43-9006 150 mg/m^2

Patients receive oral sorafenib 150 mg/m\^2 every 12 hours.

Part A: Refractory Solid Tumors: BAY 43-9006 200 mg/m^2

Patients receive oral sorafenib 200 mg/m\^2 every 12 hours.

Part A: Refractory Solid Tumors: BAY 43-9006 250 mg/m^2

Patients receive oral sorafenib 250 mg/m\^2 every 12 hours.

Part B: Refractory Leukemia: BAY 43-9006 150 mg/m^2

Patients receive oral sorafenib 150 mg/m\^2 every 12 hours.

Part B: Refractory Leukemia: BAY 43-9006 200 mg/m^2

Patients receive oral sorafenib 200 mg/m\^2 every 12 hours.

Part C: Refractory AML With FLT3-ITD Mutation:150 mg/m^2

Patients receive oral sorafenib 150 mg/m\^2 every 12 hours.

PK Cohort Expanded: BAY 43-9006 200 mg/m^2

Patients receive oral sorafenib 200 mg/m\^2 every 12 hours.

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

Analysis denominator · Participants

GroupSource count
Part A: Refractory Solid Tumors: BAY 43-9006 105 mg/m^26
Part A: Refractory Solid Tumors: BAY 43-9006 130 mg/m^23
Part A: Refractory Solid Tumors: BAY 43-9006 150 mg/m^212
Part A: Refractory Solid Tumors: BAY 43-9006 200 mg/m^27
Part A: Refractory Solid Tumors: BAY 43-9006 250 mg/m^22
Part B: Refractory Leukemia: BAY 43-9006 150 mg/m^26
Part B: Refractory Leukemia: BAY 43-9006 200 mg/m^22
Part C: Refractory AML With FLT3-ITD Mutation:150 mg/m^25
PK Cohort Expanded: BAY 43-9006 200 mg/m^212

Reported measurements

Source class 1
Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
Part A: Refractory Solid Tumors: BAY 43-9006 105 mg/m^20Not reportedNot reportedNot reportedNot reported
Part A: Refractory Solid Tumors: BAY 43-9006 130 mg/m^20Not reportedNot reportedNot reportedNot reported
Part A: Refractory Solid Tumors: BAY 43-9006 150 mg/m^20Not reportedNot reportedNot reportedNot reported
Part A: Refractory Solid Tumors: BAY 43-9006 200 mg/m^21Not reportedNot reportedNot reportedNot reported
Part A: Refractory Solid Tumors: BAY 43-9006 250 mg/m^20Not reportedNot reportedNot reportedNot reported
Part B: Refractory Leukemia: BAY 43-9006 150 mg/m^20Not reportedNot reportedNot reportedNot reported
Part B: Refractory Leukemia: BAY 43-9006 200 mg/m^20Not reportedNot reportedNot reportedNot reported
Part C: Refractory AML With FLT3-ITD Mutation:150 mg/m^20Not reportedNot reportedNot reportedNot reported
PK Cohort Expanded: BAY 43-9006 200 mg/m^20Not reportedNot reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        value
        0
      2. group Id
        OG001
        value
        0
      3. group Id
        OG002
        value
        0
      4. group Id
        OG003
        value
        1
      5. group Id
        OG004
        value
        0
      6. group Id
        OG005
        value
        0
      7. group Id
        OG006
        value
        0
      8. group Id
        OG007
        value
        0
      9. group Id
        OG008
        value
        0
denoms
  1. counts
    1. group Id
      OG000
      value
      6
    2. group Id
      OG001
      value
      3
    3. group Id
      OG002
      value
      12
    4. group Id
      OG003
      value
      7
    5. group Id
      OG004
      value
      2
    6. group Id
      OG005
      value
      6
    7. group Id
      OG006
      value
      2
    8. group Id
      OG007
      value
      5
    9. group Id
      OG008
      value
      12
    units
    Participants
description
Assess effect on tumor blood flow via DEMRI in patients with measurable soft tissue tumors.
groups
  1. description
    Patients receive oral sorafenib 105 mg/m\^2 every 12 hours.
    id
    OG000
    title
    Part A: Refractory Solid Tumors: BAY 43-9006 105 mg/m^2
  2. description
    Patients receive oral sorafenib 130 mg/m\^2 every 12 hours.
    id
    OG001
    title
    Part A: Refractory Solid Tumors: BAY 43-9006 130 mg/m^2
  3. description
    Patients receive oral sorafenib 150 mg/m\^2 every 12 hours.
    id
    OG002
    title
    Part A: Refractory Solid Tumors: BAY 43-9006 150 mg/m^2
  4. description
    Patients receive oral sorafenib 200 mg/m\^2 every 12 hours.
    id
    OG003
    title
    Part A: Refractory Solid Tumors: BAY 43-9006 200 mg/m^2
  5. description
    Patients receive oral sorafenib 250 mg/m\^2 every 12 hours.
    id
    OG004
    title
    Part A: Refractory Solid Tumors: BAY 43-9006 250 mg/m^2
  6. description
    Patients receive oral sorafenib 150 mg/m\^2 every 12 hours.
    id
    OG005
    title
    Part B: Refractory Leukemia: BAY 43-9006 150 mg/m^2
  7. description
    Patients receive oral sorafenib 200 mg/m\^2 every 12 hours.
    id
    OG006
    title
    Part B: Refractory Leukemia: BAY 43-9006 200 mg/m^2
  8. description
    Patients receive oral sorafenib 150 mg/m\^2 every 12 hours.
    id
    OG007
    title
    Part C: Refractory AML With FLT3-ITD Mutation:150 mg/m^2
  9. description
    Patients receive oral sorafenib 200 mg/m\^2 every 12 hours.
    id
    OG008
    title
    PK Cohort Expanded: BAY 43-9006 200 mg/m^2
param Type
COUNT_OF_PARTICIPANTS
population Description
There were 55 evaluable patients
reporting Status
POSTED
time Frame
Up to 2 years
title
Number of Patients With DEMRI
type
SECONDARY
unit Of Measure
Participants

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

Preserved source evidence · Not medical advice