NCT00458705 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Combination therapy with bortezomib, pegylated liposomal doxorubicin and dexamethasone (BDD) followed by either thalidomide and dexamethasone (TD) or bortezomib, thalidomide and dexamethasone in patients with symptomatic untreated high-risk or primary resistant multiple myeloma. Three cycles of BDD will be administered. Patients who respond after three cycles will receive two cycles of TD. Patients with stable or progressive disease after three cycles of BDD receive two cycles of bortezomib, thalidomide and dexamethasone. If at any point during the study a patient achieves a complete response (CR), the patient will be given the option to discontinue treatment on-study.
- id
- FG000
- title
- Combination Therapy
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 4
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Not Treated
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 45
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 40
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 5
- type
- NOT COMPLETED
- title
- Overall Study
Complete source fields
- groups
- description
- Combination therapy with bortezomib, pegylated liposomal doxorubicin and dexamethasone (BDD) followed by either thalidomide and dexamethasone (TD) or bortezomib, thalidomide and dexamethasone in patients with symptomatic untreated high-risk or primary resistant multiple myeloma. Three cycles of BDD will be administered. Patients who respond after three cycles will receive two cycles of TD. Patients with stable or progressive disease after three cycles of BDD receive two cycles of bortezomib, thalidomide and dexamethasone. If at any point during the study a patient achieves a complete response (CR), the patient will be given the option to discontinue treatment on-study.
- id
- FG000
- title
- Combination Therapy
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 4
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Not Treated
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 45
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 40
- type
- COMPLETED
- achievements
- group Id
- FG000
- 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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