NCT00089076 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Patients receive anti-cytotoxic T-lymphocyte-associated antigen-4 monoclonal antibody (MDX-010) IV over 90 minutes on day 1. Treatment repeats every 28 days for a total of 4 courses in the absence of disease progression or unacceptable toxicity.
- id
- FG000
- title
- MDX-010
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Alternate Therapy
- reasons
- group Id
- FG000
- num Subjects
- 2
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 7
- type
- Progression
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 18
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 8
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 10
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- This was a phase I/II trial. A total of 18 participants were accrued, all to the phase I portion. This trial was terminated due to study design during the phase I; therefore, the phase II portion will never open. No results from the phase II portion are available.
- recruitment Details
- Participants were recruited from 2 medical clinics in the United States between August \> 2004 and September 2007.
Complete source fields
- groups
- description
- Patients receive anti-cytotoxic T-lymphocyte-associated antigen-4 monoclonal antibody (MDX-010) IV over 90 minutes on day 1. Treatment repeats every 28 days for a total of 4 courses in the absence of disease progression or unacceptable toxicity.
- id
- FG000
- title
- MDX-010
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Alternate Therapy
- reasons
- group Id
- FG000
- num Subjects
- 2
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 7
- type
- Progression
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 18
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 8
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 10
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- This was a phase I/II trial. A total of 18 participants were accrued, all to the phase I portion. This trial was terminated due to study design during the phase I; therefore, the phase II portion will never open. No results from the phase II portion are available.
- recruitment Details
- Participants were recruited from 2 medical clinics in the United States between August \> 2004 and September 2007.
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Preserved source evidence · Not medical advice
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