NCT05255601 · OUTCOME
Number of Participants With Serious Adverse Events (SAEs) - Part B
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
- From first dose to 135 days post last dose
What was measured
Serious Adverse Event (SAE) is defined as any untoward medical occurrence that, at any dose results in death, is life-threatening, and requires inpatient hospitalization or causes prolongation of existing hospitalization. No participants enrolled in part B.
Analysis population: All treated participants in part B
Groups in this outcome
Part B
No participants enrolled in part B
| Group | Source count |
|---|---|
| Part B | 0 |
Reported measurements
No numerical measurement classes were posted for this outcome. Missing is not zero.
Complete source fields
- denoms
- counts
- group Id
- OG000
- value
- 0
- units
- Participants
- description
- Serious Adverse Event (SAE) is defined as any untoward medical occurrence that, at any dose results in death, is life-threatening, and requires inpatient hospitalization or causes prolongation of existing hospitalization. No participants enrolled in part B.
- groups
- description
- No participants enrolled in part B
- id
- OG000
- title
- Part B
- param Type
- COUNT_OF_PARTICIPANTS
- population Description
- All treated participants in part B
- reporting Status
- POSTED
- time Frame
- From first dose to 135 days post last dose
- title
- Number of Participants With Serious Adverse Events (SAEs) - Part B
- type
- SECONDARY
- unit Of Measure
- Participants
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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