NCT00932893 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Crizotinib (PF-02341066) 250 mg (administered as two 100-mg tablets and one 50-mg tablet) orally twice daily continuously in 21-day cycles. Treatment was continued until disease progression, unacceptable toxicity or withdrawal of consent occurred.
- id
- FG000
- title
- Crizotinib
- description
- Pemetrexed 500 mg per square meter (mg/m\^2) intravenous infusion over 10 minutes or docetaxel 75 mg/m\^2 intravenous infusion over 1 hour on Day 1 of 21-day cycle, as per investigator discretion. Treatment was continued until disease progression, unacceptable toxicity or withdrawal of consent occurred.
- id
- FG001
- title
- Chemotherapy
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 115
- group Id
- FG001
- num Subjects
- 24
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 8
- group Id
- FG001
- num Subjects
- 0
- type
- Lost to Follow-up
- reasons
- group Id
- FG000
- num Subjects
- 5
- group Id
- FG001
- num Subjects
- 2
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 5
- group Id
- FG001
- num Subjects
- 144
- type
- Other
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 173
- group Id
- FG001
- num Subjects
- 174
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 172
- group Id
- FG001
- num Subjects
- 171
- type
- Treated
- achievements
- group Id
- FG000
- num Subjects
- 40
- group Id
- FG001
- num Subjects
- 4
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 133
- group Id
- FG001
- num Subjects
- 170
- type
- NOT COMPLETED
- title
- Overall Study
Complete source fields
- groups
- description
- Crizotinib (PF-02341066) 250 mg (administered as two 100-mg tablets and one 50-mg tablet) orally twice daily continuously in 21-day cycles. Treatment was continued until disease progression, unacceptable toxicity or withdrawal of consent occurred.
- id
- FG000
- title
- Crizotinib
- description
- Pemetrexed 500 mg per square meter (mg/m\^2) intravenous infusion over 10 minutes or docetaxel 75 mg/m\^2 intravenous infusion over 1 hour on Day 1 of 21-day cycle, as per investigator discretion. Treatment was continued until disease progression, unacceptable toxicity or withdrawal of consent occurred.
- id
- FG001
- title
- Chemotherapy
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 115
- group Id
- FG001
- num Subjects
- 24
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 8
- group Id
- FG001
- num Subjects
- 0
- type
- Lost to Follow-up
- reasons
- group Id
- FG000
- num Subjects
- 5
- group Id
- FG001
- num Subjects
- 2
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 5
- group Id
- FG001
- num Subjects
- 144
- type
- Other
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 173
- group Id
- FG001
- num Subjects
- 174
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 172
- group Id
- FG001
- num Subjects
- 171
- type
- Treated
- achievements
- group Id
- FG000
- num Subjects
- 40
- group Id
- FG001
- num Subjects
- 4
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 133
- group Id
- FG001
- num Subjects
- 170
- type
- NOT COMPLETED
- title
- Overall Study
Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0
Preserved source evidence · Not medical advice
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