NCT03133221 · OUTCOME
Discontinuation Rate Due to Zydelig-related Adverse Events at 1 Year
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- COUNT_OF_PARTICIPANTS
- Unit
- Participants
- Interval / dispersion
- Not reported
- Time frame
- 1 year.
What was measured
The proportion of patients who discontinued the study due to Zydelig-related adverse events.
Groups in this outcome
Oral Zydelig 150 mg BID
Zydelig given orally at 150 mg twice daily continuously on 28-day cycles starting 30 to 120 days after autologous stem cell transplantation for patients with indolent or transformed indolent B-cell NHL, for up to 1 year maintenance duration. Dose withhold/modification is allowed according to tolerability/toxicity. Zydelig: Zydelig given at 150mg continuously in 28-day cycles
| Group | Source count |
|---|---|
| Oral Zydelig 150 mg BID | 17 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Oral Zydelig 150 mg BID | 5 | Not reported | Not reported | Not reported | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- value
- 5
- denoms
- counts
- group Id
- OG000
- value
- 17
- units
- Participants
- description
- The proportion of patients who discontinued the study due to Zydelig-related adverse events.
- groups
- description
- Zydelig given orally at 150 mg twice daily continuously on 28-day cycles starting 30 to 120 days after autologous stem cell transplantation for patients with indolent or transformed indolent B-cell NHL, for up to 1 year maintenance duration. Dose withhold/modification is allowed according to tolerability/toxicity. Zydelig: Zydelig given at 150mg continuously in 28-day cycles
- id
- OG000
- title
- Oral Zydelig 150 mg BID
- param Type
- COUNT_OF_PARTICIPANTS
- reporting Status
- POSTED
- time Frame
- 1 year.
- title
- Discontinuation Rate Due to Zydelig-related Adverse Events at 1 Year
- type
- PRIMARY
- unit Of Measure
- Participants
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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