NCT01822496 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Induction erlotinib for 12 weeks followed by chemotherapy (either cisplatin/etoposide or paclitaxel/carboplatin) and radiation therapy. Patients who have had no response (partial or complete) after 6 weeks of induction therapy start chemoradiation therapy immediately.
- id
- FG000
- title
- EGFR: Erlotinib
- description
- Chemotherapy (either cisplatin/etoposide or paclitaxel/carboplatin) and radiation therapy.
- id
- FG001
- title
- EGFR: No Erlotinib
- description
- Induction crizotinib for 12 weeks followed by chemotherapy (either cisplatin/etoposide or paclitaxel/carboplatin) and radiation therapy. Patients who have had no response (partial or complete) after 6 weeks of induction therapy start chemoradiation therapy immediately.
- id
- FG002
- title
- ALK: Crizotinib
- description
- Chemotherapy (either cisplatin/etoposide or paclitaxel/carboplatin) and radiation therapy.
- id
- FG003
- title
- ALK: No Crizotinib
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 2
- group Id
- FG001
- num Subjects
- 2
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 1
- type
- Protocol Violation
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 3
- type
- Withdrawal by Subject
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 16
- group Id
- FG001
- num Subjects
- 23
- group Id
- FG002
- num Subjects
- 9
- group Id
- FG003
- num Subjects
- 11
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 14
- group Id
- FG001
- num Subjects
- 21
- group Id
- FG002
- num Subjects
- 9
- group Id
- FG003
- num Subjects
- 7
- type
- Eligible
- achievements
- group Id
- FG000
- num Subjects
- 10
- group Id
- FG001
- num Subjects
- 15
- group Id
- FG002
- num Subjects
- 6
- group Id
- FG003
- num Subjects
- 4
- type
- Eligible With Disease Assessment
- achievements
- group Id
- FG000
- num Subjects
- 14
- group Id
- FG001
- num Subjects
- 20
- group Id
- FG002
- num Subjects
- 9
- group Id
- FG003
- num Subjects
- 7
- type
- Eligible and Started Study Treatment
- achievements
- group Id
- FG000
- num Subjects
- 14
- group Id
- FG001
- num Subjects
- 21
- group Id
- FG002
- num Subjects
- 9
- group Id
- FG003
- num Subjects
- 7
- comment
- Subjects contributing any data to results are considered to have completed the study
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 2
- group Id
- FG001
- num Subjects
- 2
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 4
- type
- NOT COMPLETED
- title
- Overall Study
Complete source fields
- groups
- description
- Induction erlotinib for 12 weeks followed by chemotherapy (either cisplatin/etoposide or paclitaxel/carboplatin) and radiation therapy. Patients who have had no response (partial or complete) after 6 weeks of induction therapy start chemoradiation therapy immediately.
- id
- FG000
- title
- EGFR: Erlotinib
- description
- Chemotherapy (either cisplatin/etoposide or paclitaxel/carboplatin) and radiation therapy.
- id
- FG001
- title
- EGFR: No Erlotinib
- description
- Induction crizotinib for 12 weeks followed by chemotherapy (either cisplatin/etoposide or paclitaxel/carboplatin) and radiation therapy. Patients who have had no response (partial or complete) after 6 weeks of induction therapy start chemoradiation therapy immediately.
- id
- FG002
- title
- ALK: Crizotinib
- description
- Chemotherapy (either cisplatin/etoposide or paclitaxel/carboplatin) and radiation therapy.
- id
- FG003
- title
- ALK: No Crizotinib
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 2
- group Id
- FG001
- num Subjects
- 2
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 1
- type
- Protocol Violation
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 3
- type
- Withdrawal by Subject
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 16
- group Id
- FG001
- num Subjects
- 23
- group Id
- FG002
- num Subjects
- 9
- group Id
- FG003
- num Subjects
- 11
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 14
- group Id
- FG001
- num Subjects
- 21
- group Id
- FG002
- num Subjects
- 9
- group Id
- FG003
- num Subjects
- 7
- type
- Eligible
- achievements
- group Id
- FG000
- num Subjects
- 10
- group Id
- FG001
- num Subjects
- 15
- group Id
- FG002
- num Subjects
- 6
- group Id
- FG003
- num Subjects
- 4
- type
- Eligible With Disease Assessment
- achievements
- group Id
- FG000
- num Subjects
- 14
- group Id
- FG001
- num Subjects
- 20
- group Id
- FG002
- num Subjects
- 9
- group Id
- FG003
- num Subjects
- 7
- type
- Eligible and Started Study Treatment
- achievements
- group Id
- FG000
- num Subjects
- 14
- group Id
- FG001
- num Subjects
- 21
- group Id
- FG002
- num Subjects
- 9
- group Id
- FG003
- num Subjects
- 7
- comment
- Subjects contributing any data to results are considered to have completed the study
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 2
- group Id
- FG001
- num Subjects
- 2
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 4
- type
- NOT COMPLETED
- title
- Overall Study
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Preserved source evidence · Not medical advice
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