NCT04042376 · OUTCOME
Very Good Partial Response (VGPR) or Better Response Rate
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- NUMBER
- Unit
- Percentage of Participants
- Interval / dispersion
- 90% Confidence Interval
- Time frame
- From start of the treatment (Day 1) up to 49.3 months
What was measured
VGPR or better response rate was defined as the percentage of participants who achieved VGPR or better according to the modified sixth IWWM (NCCN 2019) criteria as assessed by the investigator. VGPR: \>=90% reduction of serum IgM from baseline or normal serum IgM values, with reduction in lymphadenopathy/splenomegaly if present at baseline.
Analysis population: All treated analysis set included all enrolled participants who received at least 1 dose of study drug.
Groups in this outcome
Ibrutinib 420 mg
Participants with relapsed or refractory waldenstrom's macroglobulinemia received ibrutinib 420 milligrams (mg) (3\*140 mg capsules) orally once daily from Day 1 of Week 1 until disease progression, unacceptable toxicity, whichever occurs first.
| Group | Source count |
|---|---|
| Ibrutinib 420 mg | 17 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Ibrutinib 420 mg | 5.9 | Not reported | 0.3 | 25.0 | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- lower Limit
- 0.3
- upper Limit
- 25.0
- value
- 5.9
- denoms
- counts
- group Id
- OG000
- value
- 17
- units
- Participants
- description
- VGPR or better response rate was defined as the percentage of participants who achieved VGPR or better according to the modified sixth IWWM (NCCN 2019) criteria as assessed by the investigator. VGPR: \>=90% reduction of serum IgM from baseline or normal serum IgM values, with reduction in lymphadenopathy/splenomegaly if present at baseline.
- dispersion Type
- 90% Confidence Interval
- groups
- description
- Participants with relapsed or refractory waldenstrom's macroglobulinemia received ibrutinib 420 milligrams (mg) (3\*140 mg capsules) orally once daily from Day 1 of Week 1 until disease progression, unacceptable toxicity, whichever occurs first.
- id
- OG000
- title
- Ibrutinib 420 mg
- param Type
- NUMBER
- population Description
- All treated analysis set included all enrolled participants who received at least 1 dose of study drug.
- reporting Status
- POSTED
- time Frame
- From start of the treatment (Day 1) up to 49.3 months
- title
- Very Good Partial Response (VGPR) or Better Response Rate
- type
- SECONDARY
- unit Of Measure
- Percentage of Participants
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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