TriangleNCT03682536 · OUTCOME
Percentage of Participants Achieving Red Blood Cell Transfusion Independence (RBC-TI) for ≥ 12 Weeks (84 Days)
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- NUMBER
- Unit
- Percent of participants
- Interval / dispersion
- 95% Confidence Interval
- Time frame
- Week 1 through Week 24
What was measured
Percentage of participants who are RBC transfusion-free over a consecutive 84-day period.
Analysis population: ITT Population - all randomized participants regardless of whether or not the participant received treatment.
Groups in this outcome
Luspatercept
Starting dose of 1.0 mg/kg subcutaneous injection every 3 weeks (21 days; Q3W). Dose levels can be increased in a stepwise manner beyond the starting dose to 1.33 mg/kg, and up to a maximum of 1.75 mg/kg.
Epoetin Alfa
Starting dose of 450 IU/kg (maximum total starting dose is 40,000 IU) subcutaneous injection once every week (7 days; QW). Dose levels can be increased in a stepwise manner beyond the starting dose to 787.5 IU/kg, and up to a maximum of 1,050 IU/kg (with a maximum total dose of 80,000 IU).
| Group | Source count |
|---|---|
| Luspatercept | 182 |
| Epoetin Alfa | 181 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Luspatercept | 68.1 | Not reported | 60.8 | 74.8 | Not reported |
| Epoetin Alfa | 48.6 | Not reported | 41.1 | 56.1 | Not reported |
Source statistical analyses
- ci Lower Limit
- 1.6
- ci Num Sides
- TWO_SIDED
- ci Pct Value
- 95
- ci Upper Limit
- 4.0
- group Ids
- OG000
- OG001
- non Inferiority Type
- SUPERIORITY
- p Value
- <.0001
- param Type
- Odds Ratio (OR)
- param Value
- 2.5
- statistical Method
- Cochran-Mantel-Haenszel
Complete source fields
- analyses
- ci Lower Limit
- 1.6
- ci Num Sides
- TWO_SIDED
- ci Pct Value
- 95
- ci Upper Limit
- 4.0
- group Ids
- OG000
- OG001
- non Inferiority Type
- SUPERIORITY
- p Value
- <.0001
- param Type
- Odds Ratio (OR)
- param Value
- 2.5
- statistical Method
- Cochran-Mantel-Haenszel
- classes
- categories
- measurements
- group Id
- OG000
- lower Limit
- 60.8
- upper Limit
- 74.8
- value
- 68.1
- group Id
- OG001
- lower Limit
- 41.1
- upper Limit
- 56.1
- value
- 48.6
- denoms
- counts
- group Id
- OG000
- value
- 182
- group Id
- OG001
- value
- 181
- units
- Participants
- description
- Percentage of participants who are RBC transfusion-free over a consecutive 84-day period.
- dispersion Type
- 95% Confidence Interval
- groups
- description
- Starting dose of 1.0 mg/kg subcutaneous injection every 3 weeks (21 days; Q3W). Dose levels can be increased in a stepwise manner beyond the starting dose to 1.33 mg/kg, and up to a maximum of 1.75 mg/kg.
- id
- OG000
- title
- Luspatercept
- description
- Starting dose of 450 IU/kg (maximum total starting dose is 40,000 IU) subcutaneous injection once every week (7 days; QW). Dose levels can be increased in a stepwise manner beyond the starting dose to 787.5 IU/kg, and up to a maximum of 1,050 IU/kg (with a maximum total dose of 80,000 IU).
- id
- OG001
- title
- Epoetin Alfa
- param Type
- NUMBER
- population Description
- ITT Population - all randomized participants regardless of whether or not the participant received treatment.
- reporting Status
- POSTED
- time Frame
- Week 1 through Week 24
- title
- Percentage of Participants Achieving Red Blood Cell Transfusion Independence (RBC-TI) for ≥ 12 Weeks (84 Days)
- type
- SECONDARY
- unit Of Measure
- Percent of participants
Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0
Preserved source evidence · Not medical advice