NCT00459862 · OUTCOME
Determine the Clinical Toxicities of This Drug in This Participant Population.
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- NUMBER
- Unit
- participants
- Interval / dispersion
- Not reported
- Time frame
- Participants will be evaluated every cycle during treatment
What was measured
The number of participants with a reported Grade 3, Grade 4, and Grade 5 toxicity, regardless of attribution, will be tabulated.
Analysis population: All 34 participants were evaluable for adverse events.
Groups in this outcome
Arm I
Patients receive 800 mg oral pazopanib hydrochloride once daily on days 1-21. Treatment repeats every 21 days for 2 years in the absence of disease progression or unacceptable toxicity.
| Group | Source count |
|---|---|
| Arm I | 34 |
Reported measurements
Grade 3 or Higher
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Arm I | 23 | Not reported | Not reported | Not reported | Not reported |
Grade 4 or Higher
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Arm I | 5 | Not reported | Not reported | Not reported | Not reported |
Grade 5
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Arm I | 3 | Not reported | Not reported | Not reported | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- value
- 23
- title
- Grade 3 or Higher
- categories
- measurements
- group Id
- OG000
- value
- 5
- title
- Grade 4 or Higher
- categories
- measurements
- group Id
- OG000
- value
- 3
- title
- Grade 5
- denoms
- counts
- group Id
- OG000
- value
- 34
- units
- Participants
- description
- The number of participants with a reported Grade 3, Grade 4, and Grade 5 toxicity, regardless of attribution, will be tabulated.
- groups
- description
- Patients receive 800 mg oral pazopanib hydrochloride once daily on days 1-21. Treatment repeats every 21 days for 2 years in the absence of disease progression or unacceptable toxicity.
- id
- OG000
- title
- Arm I
- param Type
- NUMBER
- population Description
- All 34 participants were evaluable for adverse events.
- reporting Status
- POSTED
- time Frame
- Participants will be evaluated every cycle during treatment
- title
- Determine the Clinical Toxicities of This Drug in This Participant Population.
- type
- SECONDARY
- unit Of Measure
- participants
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
Triangle