NCT00720304 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Weekly docetaxel (20 mg/m2), EGF-R inhibition: Erlotinib 150 mg/day (prior to, during and up to two years following XRT)
- id
- FG000
- title
- CASE5307 - Oral Erlotinib Hydrochloride
- description
- Participants from CWRU1301 - NCT00049283 who received Docetaxel 20 mg/m2/wk Erlotinib 150 mg/day XRT
- id
- FG001
- title
- Participants From CWRU1301
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 14
- group Id
- FG001
- num Subjects
- 1
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 0
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 5
- group Id
- FG001
- num Subjects
- 2
- type
- Physician Decision
- reasons
- group Id
- FG000
- num Subjects
- 3
- group Id
- FG001
- num Subjects
- 1
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 6
- group Id
- FG001
- num Subjects
- 1
- type
- Disease progression
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 37
- group Id
- FG001
- num Subjects
- 6
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 8
- group Id
- FG001
- num Subjects
- 1
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 29
- group Id
- FG001
- num Subjects
- 5
- type
- NOT COMPLETED
- title
- Overall Study
Complete source fields
- groups
- description
- Weekly docetaxel (20 mg/m2), EGF-R inhibition: Erlotinib 150 mg/day (prior to, during and up to two years following XRT)
- id
- FG000
- title
- CASE5307 - Oral Erlotinib Hydrochloride
- description
- Participants from CWRU1301 - NCT00049283 who received Docetaxel 20 mg/m2/wk Erlotinib 150 mg/day XRT
- id
- FG001
- title
- Participants From CWRU1301
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 14
- group Id
- FG001
- num Subjects
- 1
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 0
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 5
- group Id
- FG001
- num Subjects
- 2
- type
- Physician Decision
- reasons
- group Id
- FG000
- num Subjects
- 3
- group Id
- FG001
- num Subjects
- 1
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 6
- group Id
- FG001
- num Subjects
- 1
- type
- Disease progression
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 37
- group Id
- FG001
- num Subjects
- 6
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 8
- group Id
- FG001
- num Subjects
- 1
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 29
- group Id
- FG001
- num Subjects
- 5
- type
- NOT COMPLETED
- title
- Overall Study
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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