NCT06655818 · BASELINE
Baseline characteristics
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- denoms
- counts
- group Id
- BG000
- value
- 4
- units
- Participants
- groups
- description
- Participants with Relapsed/Refractory Multiple Myeloma (RRMM) received 1.9 milligram (mg)/kilogram (kg) belantamab mafodotin intravenous (IV) infusion as powder for solution once every 3 weeks (Q3W) infused over 30- 60 minutes on day 1 of 21-day cycles in combination with 500 mg dostarlimab as a 30-minute IV infusion 1 hour after belantamab mafodotin end of infusion (EOI) on day 1 of 21-day cycles (Q3W).
- id
- BG000
- title
- 1.9 mg/kg Belantamab Mafodotin + 500mg Dostarlimab
- measures
- classes
- categories
- measurements
- group Id
- BG000
- spread
- 9.83
- value
- 70.0
- dispersion Type
- STANDARD_DEVIATION
- param Type
- MEAN
- title
- Age, Continuous
- unit Of Measure
- YEAR
- classes
- categories
- measurements
- group Id
- BG000
- value
- 4
- title
- Males and Females
- description
- Gender categories (with 0\<n\<11) are combined into 'Males and Females' category to maintain participant confidentiality and privacy as the study is evaluating a rare disease.
- param Type
- COUNT_OF_PARTICIPANTS
- title
- Sex/Gender, Customized
- unit Of Measure
- Participants
- classes
- categories
- measurements
- group Id
- BG000
- value
- 4
- title
- Others
- description
- Race categories (with 0\<n\<11) are combined into 'Others' category to maintain participant confidentiality and privacy as the study is evaluating a rare disease.
- param Type
- COUNT_OF_PARTICIPANTS
- title
- Race/Ethnicity, Customized
- unit Of Measure
- Participants
Complete source fields
- denoms
- counts
- group Id
- BG000
- value
- 4
- units
- Participants
- groups
- description
- Participants with Relapsed/Refractory Multiple Myeloma (RRMM) received 1.9 milligram (mg)/kilogram (kg) belantamab mafodotin intravenous (IV) infusion as powder for solution once every 3 weeks (Q3W) infused over 30- 60 minutes on day 1 of 21-day cycles in combination with 500 mg dostarlimab as a 30-minute IV infusion 1 hour after belantamab mafodotin end of infusion (EOI) on day 1 of 21-day cycles (Q3W).
- id
- BG000
- title
- 1.9 mg/kg Belantamab Mafodotin + 500mg Dostarlimab
- measures
- classes
- categories
- measurements
- group Id
- BG000
- spread
- 9.83
- value
- 70.0
- dispersion Type
- STANDARD_DEVIATION
- param Type
- MEAN
- title
- Age, Continuous
- unit Of Measure
- YEAR
- classes
- categories
- measurements
- group Id
- BG000
- value
- 4
- title
- Males and Females
- description
- Gender categories (with 0\<n\<11) are combined into 'Males and Females' category to maintain participant confidentiality and privacy as the study is evaluating a rare disease.
- param Type
- COUNT_OF_PARTICIPANTS
- title
- Sex/Gender, Customized
- unit Of Measure
- Participants
- classes
- categories
- measurements
- group Id
- BG000
- value
- 4
- title
- Others
- description
- Race categories (with 0\<n\<11) are combined into 'Others' category to maintain participant confidentiality and privacy as the study is evaluating a rare disease.
- param Type
- COUNT_OF_PARTICIPANTS
- title
- Race/Ethnicity, Customized
- unit Of Measure
- Participants
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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