NCT02721732 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- MK-3475: 200 mg of MK-3475 administered intravenously on Day 1 of every 21-day cycle
- id
- FG000
- title
- Cohort 1: Squamous Cell Carcinoma of the Skin
- description
- MK-3475: 200 mg of MK-3475 administered intravenously on Day 1 of every 21-day cycle
- id
- FG001
- title
- Cohort 2: Small Cell Malignancies of Nonpulmonary Origin
- description
- MK-3475: 200 mg of MK-3475 administered intravenously on Day 1 of every 21-day cycle
- id
- FG002
- title
- Cohort 3: Adrenocortical Carcinoma
- description
- MK-3475: 200 mg of MK-3475 administered intravenously on Day 1 of every 21-day cycle
- id
- FG003
- title
- Cohort 4: Medullary Renal Cell Carcinoma
- description
- MK-3475: 200 mg of MK-3475 administered intravenously on Day 1 of every 21-day cycle
- id
- FG004
- title
- Cohort 5: Carcinoma of Unknown Primary
- description
- MK-3475: 200 mg of MK-3475 administered intravenously on Day 1 of every 21-day cycle
- id
- FG005
- title
- Cohort 6: Penile Carcinoma
- description
- MK-3475: 200 mg of MK-3475 administered intravenously on Day 1 of every 21-day cycle
- id
- FG006
- title
- Cohort 7: Vascular Sarcoma
- description
- MK-3475: 200 mg of MK-3475 administered intravenously on Day 1 of every 21-day cycle
- id
- FG007
- title
- Cohort 8: Germ Cell Tumor
- description
- MK-3475: 200 mg of MK-3475 administered intravenously on Day 1 of every 21-day cycle
- id
- FG008
- title
- Cohort 9: Paraganglioma-pheochromocytoma
- description
- MK-3475: 200 mg of MK-3475 administered intravenously on Day 1 of every 21-day cycle
- id
- FG009
- title
- Cohort 10: Other Rare Tumor Histologies
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 2
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 2
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 1
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 1
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 1
- group Id
- FG009
- num Subjects
- 1
- type
- Adverse Event
- 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
- 1
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 1
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 1
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 12
- group Id
- FG001
- num Subjects
- 11
- group Id
- FG002
- num Subjects
- 18
- group Id
- FG003
- num Subjects
- 5
- group Id
- FG004
- num Subjects
- 21
- group Id
- FG005
- num Subjects
- 2
- group Id
- FG006
- num Subjects
- 8
- group Id
- FG007
- num Subjects
- 11
- group Id
- FG008
- num Subjects
- 10
- group Id
- FG009
- num Subjects
- 20
- type
- Lack of Efficacy
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 1
- 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
- type
- Physician Decision
- reasons
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 3
- 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
- 1
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 1
- 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
- 1
- type
- Participant Choice
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 1
- 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
- type
- Progression and Exclusion from study due to changed diagnosis
- reasons
- group Id
- FG000
- num Subjects
- 1
- 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
- 1
- type
- Progression and withdrew consent
- 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
- 1
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- type
- No evidence of tumor following radical surgery
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 20
- group Id
- FG001
- num Subjects
- 12
- group Id
- FG002
- num Subjects
- 24
- group Id
- FG003
- num Subjects
- 5
- group Id
- FG004
- num Subjects
- 29
- group Id
- FG005
- num Subjects
- 3
- group Id
- FG006
- num Subjects
- 11
- group Id
- FG007
- num Subjects
- 12
- group Id
- FG008
- num Subjects
- 13
- group Id
- FG009
- num Subjects
- 28
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 3
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 2
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 3
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 2
- group Id
- FG009
- num Subjects
- 3
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 17
- group Id
- FG001
- num Subjects
- 12
- group Id
- FG002
- num Subjects
- 22
- group Id
- FG003
- num Subjects
- 5
- group Id
- FG004
- num Subjects
- 26
- group Id
- FG005
- num Subjects
- 3
- group Id
- FG006
- num Subjects
- 11
- group Id
- FG007
- num Subjects
- 12
- group Id
- FG008
- num Subjects
- 11
- group Id
- FG009
- num Subjects
- 25
- type
- NOT COMPLETED
- title
- Overall Study
- recruitment Details
- This is a single-center, open-label, phase II trial of pembrolizumab (MK-3475) in patients with and without programmed death-ligand 1 (PD-L1) positive advanced tumors conducted at the University of Texas MD Anderson Cancer Center
Complete source fields
- groups
- description
- MK-3475: 200 mg of MK-3475 administered intravenously on Day 1 of every 21-day cycle
- id
- FG000
- title
- Cohort 1: Squamous Cell Carcinoma of the Skin
- description
- MK-3475: 200 mg of MK-3475 administered intravenously on Day 1 of every 21-day cycle
- id
- FG001
- title
- Cohort 2: Small Cell Malignancies of Nonpulmonary Origin
- description
- MK-3475: 200 mg of MK-3475 administered intravenously on Day 1 of every 21-day cycle
- id
- FG002
- title
- Cohort 3: Adrenocortical Carcinoma
- description
- MK-3475: 200 mg of MK-3475 administered intravenously on Day 1 of every 21-day cycle
- id
- FG003
- title
- Cohort 4: Medullary Renal Cell Carcinoma
- description
- MK-3475: 200 mg of MK-3475 administered intravenously on Day 1 of every 21-day cycle
- id
- FG004
- title
- Cohort 5: Carcinoma of Unknown Primary
- description
- MK-3475: 200 mg of MK-3475 administered intravenously on Day 1 of every 21-day cycle
- id
- FG005
- title
- Cohort 6: Penile Carcinoma
- description
- MK-3475: 200 mg of MK-3475 administered intravenously on Day 1 of every 21-day cycle
- id
- FG006
- title
- Cohort 7: Vascular Sarcoma
- description
- MK-3475: 200 mg of MK-3475 administered intravenously on Day 1 of every 21-day cycle
- id
- FG007
- title
- Cohort 8: Germ Cell Tumor
- description
- MK-3475: 200 mg of MK-3475 administered intravenously on Day 1 of every 21-day cycle
- id
- FG008
- title
- Cohort 9: Paraganglioma-pheochromocytoma
- description
- MK-3475: 200 mg of MK-3475 administered intravenously on Day 1 of every 21-day cycle
- id
- FG009
- title
- Cohort 10: Other Rare Tumor Histologies
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 2
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 2
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 1
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 1
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 1
- group Id
- FG009
- num Subjects
- 1
- type
- Adverse Event
- 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
- 1
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 1
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 1
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 12
- group Id
- FG001
- num Subjects
- 11
- group Id
- FG002
- num Subjects
- 18
- group Id
- FG003
- num Subjects
- 5
- group Id
- FG004
- num Subjects
- 21
- group Id
- FG005
- num Subjects
- 2
- group Id
- FG006
- num Subjects
- 8
- group Id
- FG007
- num Subjects
- 11
- group Id
- FG008
- num Subjects
- 10
- group Id
- FG009
- num Subjects
- 20
- type
- Lack of Efficacy
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 1
- 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
- type
- Physician Decision
- reasons
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 3
- 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
- 1
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 1
- 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
- 1
- type
- Participant Choice
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 1
- 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
- type
- Progression and Exclusion from study due to changed diagnosis
- reasons
- group Id
- FG000
- num Subjects
- 1
- 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
- 1
- type
- Progression and withdrew consent
- 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
- 1
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- type
- No evidence of tumor following radical surgery
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 20
- group Id
- FG001
- num Subjects
- 12
- group Id
- FG002
- num Subjects
- 24
- group Id
- FG003
- num Subjects
- 5
- group Id
- FG004
- num Subjects
- 29
- group Id
- FG005
- num Subjects
- 3
- group Id
- FG006
- num Subjects
- 11
- group Id
- FG007
- num Subjects
- 12
- group Id
- FG008
- num Subjects
- 13
- group Id
- FG009
- num Subjects
- 28
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 3
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 2
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 3
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 2
- group Id
- FG009
- num Subjects
- 3
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 17
- group Id
- FG001
- num Subjects
- 12
- group Id
- FG002
- num Subjects
- 22
- group Id
- FG003
- num Subjects
- 5
- group Id
- FG004
- num Subjects
- 26
- group Id
- FG005
- num Subjects
- 3
- group Id
- FG006
- num Subjects
- 11
- group Id
- FG007
- num Subjects
- 12
- group Id
- FG008
- num Subjects
- 11
- group Id
- FG009
- num Subjects
- 25
- type
- NOT COMPLETED
- title
- Overall Study
- recruitment Details
- This is a single-center, open-label, phase II trial of pembrolizumab (MK-3475) in patients with and without programmed death-ligand 1 (PD-L1) positive advanced tumors conducted at the University of Texas MD Anderson Cancer Center
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
Triangle