NCT02393248 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Participants self-administered oral pemigatinib 1/2/4 milligrams (mg) once daily (QD) on a 2-weeks-on therapy and 1-week-off therapy schedule. The treatment cycle consisted of: Days 1 through 14: pemigatinib QD; Days 15 through 21: treatment break.
- id
- FG000
- title
- Part 1: Intermittent Pemigatinib 1/2/4 mg QD
- description
- Participants self-administered oral pemigatinib 6 mg QD on a 2-weeks-on therapy and 1-week-off therapy schedule. The treatment cycle consisted of: Days 1 through 14: pemigatinib QD; Days 15 through 21: treatment break.
- id
- FG001
- title
- Part 1: Intermittent Pemigatinib 6 mg QD
- description
- Participants self-administered oral pemigatinib 9 mg QD on a 2-weeks-on therapy and 1-week-off therapy schedule. The treatment cycle consisted of: Days 1 through 14: pemigatinib QD; Days 15 through 21: treatment break.
- id
- FG002
- title
- Part 1: Intermittent Pemigatinib 9 mg QD
- description
- Participants self-administered oral pemigatinib 13.5 mg QD on a 2-weeks-on therapy and 1-week-off therapy schedule. The treatment cycle consisted of: Days 1 through 14: pemigatinib QD; Days 15 through 21: treatment break.
- id
- FG003
- title
- Part 1: Intermittent Pemigatinib 13.5 mg QD
- description
- Participants self-administered oral pemigatinib 20 mg QD on a 2-weeks-on therapy and 1-week-off therapy schedule. The treatment cycle consisted of: Days 1 through 14: pemigatinib QD; Days 15 through 21: treatment break.
- id
- FG004
- title
- Part 1: Intermittent Pemigatinib 20 mg QD
- description
- Participants self-administered oral pemigatinib 9 mg QD on Days 1 through 21 of each 21-day cycle.
- id
- FG005
- title
- Part 1: Continuous Pemigatinib 9 mg QD
- description
- Participants self-administered oral pemigatinib 13.5 mg QD on Days 1 through 21 of each 21-day cycle.
- id
- FG006
- title
- Part 1: Continuous Pemigatinib 13.5 mg QD
- description
- Participants self-administered oral pemigatinib 20 mg QD on Days 1 through 21 of each 21-day cycle.
- id
- FG007
- title
- Part 1: Continuous Pemigatinib 20 mg QD
- description
- Participants self-administered oral pemigatinib 7.5 mg twice daily (BID) on Days 1 through 21 of each 21-day cycle.
- id
- FG008
- title
- Part 1: Continuous Pemigatinib 7.5 mg BID
- description
- Participants self-administered oral pemigatinib 10 mg BID on Days 1 through 21 of each 21-day cycle.
- id
- FG009
- title
- Part 1: Continuous Pemigatinib 10 mg BID
- description
- Participants self-administered oral pemigatinib 9 mg QD on a 2-weeks-on therapy and 1-week-off therapy schedule. The treatment cycle consisted of: Days 1 through 14: pemigatinib QD; Days 15 through 21: treatment break.
- id
- FG010
- title
- Part 2: Intermittent Pemigatinib 9 mg QD
- description
- Participants self-administered oral pemigatinib 13.5 mg QD on a 2-weeks-on therapy and 1-week-off therapy schedule. The treatment cycle consisted of: Days 1 through 14: pemigatinib QD; Days 15 through 21: treatment break.
- id
- FG011
- title
- Part 2: Intermittent Pemigatinib 13.5 mg QD
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 1
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 1
- group Id
- FG006
- num Subjects
- 1
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 0
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 1
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 0
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- Disease Progression
- reasons
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- num Subjects
- 2
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- num Subjects
- 2
- group Id
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- 3
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- FG003
- num Subjects
- 6
- group Id
- FG004
- num Subjects
- 6
- group Id
- FG005
- num Subjects
- 6
- group Id
- FG006
- num Subjects
- 5
- group Id
- FG007
- num Subjects
- 8
- group Id
- FG008
- num Subjects
- 4
- group Id
- FG009
- num Subjects
- 2
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 0
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
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- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 0
- type
- Lost to Follow-up
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 2
- group Id
- FG006
- num Subjects
- 2
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 1
- group Id
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- 0
- group Id
- FG011
- num Subjects
- 0
- type
- Study Terminated by Sponsor
- reasons
- group Id
- FG000
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- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
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- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
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- num Subjects
- 1
- group Id
- FG007
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- 0
- group Id
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- num Subjects
- 0
- group Id
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- num Subjects
- 0
- group Id
- FG010
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- 0
- group Id
- FG011
- num Subjects
- 0
- type
- Clinical Decline; Withdrew by Physician
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 3
- group Id
- FG001
- num Subjects
- 4
- group Id
- FG002
- num Subjects
- 3
- group Id
- FG003
- num Subjects
- 6
- group Id
- FG004
- num Subjects
- 6
- group Id
- FG005
- num Subjects
- 9
- group Id
- FG006
- num Subjects
- 10
- group Id
- FG007
- num Subjects
- 9
- group Id
- FG008
- num Subjects
- 4
- group Id
- FG009
- num Subjects
- 3
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 0
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 1
- group Id
- FG007
- num Subjects
- 1
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 0
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 3
- group Id
- FG001
- num Subjects
- 4
- group Id
- FG002
- num Subjects
- 3
- group Id
- FG003
- num Subjects
- 6
- group Id
- FG004
- num Subjects
- 6
- group Id
- FG005
- num Subjects
- 9
- group Id
- FG006
- num Subjects
- 9
- group Id
- FG007
- num Subjects
- 8
- group Id
- FG008
- num Subjects
- 4
- group Id
- FG009
- num Subjects
- 3
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 0
- type
- NOT COMPLETED
- title
- Part 1: Monotherapy Dose Escalation
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 13
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
- num Subjects
- 1
- group Id
- FG011
- num Subjects
- 1
- type
- Disease Progression
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
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- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
- num Subjects
- 3
- group Id
- FG011
- num Subjects
- 29
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
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- 0
- group Id
- FG002
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- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
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- 0
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- FG007
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- 0
- group Id
- FG008
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- 0
- group Id
- FG009
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- 0
- group Id
- FG010
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- 0
- group Id
- FG011
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- 1
- type
- Study Terminated by Sponsor
- milestones
- achievements
- group Id
- FG000
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- 0
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- 0
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- 0
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- group Id
- FG011
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- type
- STARTED
- achievements
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- FG000
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- type
- COMPLETED
- achievements
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- 0
- group Id
- FG010
- num Subjects
- 4
- group Id
- FG011
- num Subjects
- 44
- type
- NOT COMPLETED
- title
- Part 2: Monotherapy Dose Expansion
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 0
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
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- 0
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- FG005
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- 0
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- FG007
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- group Id
- FG008
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- group Id
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- group Id
- FG011
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- 0
- type
- Death
- reasons
- group Id
- FG000
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- 0
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- FG001
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- 0
- group Id
- FG002
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- 0
- group Id
- FG003
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- 0
- group Id
- FG004
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- 0
- group Id
- FG005
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- 0
- group Id
- FG006
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- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 0
- type
- Study Terminated by Sponsor
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
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- 0
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
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- 0
- group Id
- FG011
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- 0
- type
- Disease Progression
- reasons
- group Id
- FG000
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- 0
- group Id
- FG001
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- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 0
- type
- Lost to Follow-up
- reasons
- group Id
- FG000
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- 0
- group Id
- FG001
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- 0
- group Id
- FG002
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- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
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- 0
- group Id
- FG006
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- 0
- group Id
- FG007
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- 0
- group Id
- FG008
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- 0
- group Id
- FG009
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- 0
- group Id
- FG010
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- 0
- group Id
- FG011
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- 0
- type
- Rolled Over to Another Protocol after Receiving Same Treatment
- reasons
- group Id
- FG000
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- 0
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- FG001
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- 0
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- FG002
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- 0
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- FG003
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- 0
- group Id
- FG004
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- 0
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- FG005
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- 0
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- FG006
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- 0
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- FG007
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- 0
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- FG008
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- 0
- group Id
- FG009
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- 0
- group Id
- FG010
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- 0
- group Id
- FG011
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- 0
- type
- Adverse Event
- reasons
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- FG000
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- 0
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- 0
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- 0
- group Id
- FG003
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- 0
- group Id
- FG004
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- 0
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- 0
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- 0
- type
- Placed on Hospice; Declined Further Follow-up
- milestones
- achievements
- group Id
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- 0
- group Id
- FG004
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- 0
- group Id
- FG005
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- group Id
- FG006
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- 0
- group Id
- FG007
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- 0
- group Id
- FG008
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- 0
- group Id
- FG009
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- group Id
- FG010
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- 0
- group Id
- FG011
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- 0
- type
- STARTED
- achievements
- group Id
- FG000
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- 0
- group Id
- FG001
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- 0
- group Id
- FG002
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- 0
- group Id
- FG003
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- 0
- group Id
- FG004
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- 0
- group Id
- FG005
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- 0
- group Id
- FG006
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- 0
- group Id
- FG007
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- 0
- group Id
- FG008
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- 0
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 0
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- group Id
- FG010
- num Subjects
- 0
- group Id
- FG011
- num Subjects
- 0
- type
- NOT COMPLETED
- title
- Part 3: Combination Therapy
- recruitment Details
- This study was conducted at 15 study sites: 14 sites in the United States and 1 site in Denmark. The study was conducted in 3 parts. Participants self-administered once daily doses of pemigatinib on a 2-weeks-on/1-week-off therapy (intermittent) or continuous schedule in 21-day cycles. Participants also self-administered twice daily doses of pemigatinib on a continuous schedule.
Complete source fields
- groups
- description
- Participants self-administered oral pemigatinib 1/2/4 milligrams (mg) once daily (QD) on a 2-weeks-on therapy and 1-week-off therapy schedule. The treatment cycle consisted of: Days 1 through 14: pemigatinib QD; Days 15 through 21: treatment break.
- id
- FG000
- title
- Part 1: Intermittent Pemigatinib 1/2/4 mg QD
- description
- Participants self-administered oral pemigatinib 6 mg QD on a 2-weeks-on therapy and 1-week-off therapy schedule. The treatment cycle consisted of: Days 1 through 14: pemigatinib QD; Days 15 through 21: treatment break.
- id
- FG001
- title
- Part 1: Intermittent Pemigatinib 6 mg QD
- description
- Participants self-administered oral pemigatinib 9 mg QD on a 2-weeks-on therapy and 1-week-off therapy schedule. The treatment cycle consisted of: Days 1 through 14: pemigatinib QD; Days 15 through 21: treatment break.
- id
- FG002
- title
- Part 1: Intermittent Pemigatinib 9 mg QD
- description
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- id
- FG003
- title
- Part 1: Intermittent Pemigatinib 13.5 mg QD
- description
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- id
- FG004
- title
- Part 1: Intermittent Pemigatinib 20 mg QD
- description
- Participants self-administered oral pemigatinib 9 mg QD on Days 1 through 21 of each 21-day cycle.
- id
- FG005
- title
- Part 1: Continuous Pemigatinib 9 mg QD
- description
- Participants self-administered oral pemigatinib 13.5 mg QD on Days 1 through 21 of each 21-day cycle.
- id
- FG006
- title
- Part 1: Continuous Pemigatinib 13.5 mg QD
- description
- Participants self-administered oral pemigatinib 20 mg QD on Days 1 through 21 of each 21-day cycle.
- id
- FG007
- title
- Part 1: Continuous Pemigatinib 20 mg QD
- description
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- id
- FG008
- title
- Part 1: Continuous Pemigatinib 7.5 mg BID
- description
- Participants self-administered oral pemigatinib 10 mg BID on Days 1 through 21 of each 21-day cycle.
- id
- FG009
- title
- Part 1: Continuous Pemigatinib 10 mg BID
- description
- Participants self-administered oral pemigatinib 9 mg QD on a 2-weeks-on therapy and 1-week-off therapy schedule. The treatment cycle consisted of: Days 1 through 14: pemigatinib QD; Days 15 through 21: treatment break.
- id
- FG010
- title
- Part 2: Intermittent Pemigatinib 9 mg QD
- description
- Participants self-administered oral pemigatinib 13.5 mg QD on a 2-weeks-on therapy and 1-week-off therapy schedule. The treatment cycle consisted of: Days 1 through 14: pemigatinib QD; Days 15 through 21: treatment break.
- id
- FG011
- title
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- title
- Part 3: Combination Therapy
- recruitment Details
- This study was conducted at 15 study sites: 14 sites in the United States and 1 site in Denmark. The study was conducted in 3 parts. Participants self-administered once daily doses of pemigatinib on a 2-weeks-on/1-week-off therapy (intermittent) or continuous schedule in 21-day cycles. Participants also self-administered twice daily doses of pemigatinib on a continuous schedule.
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