NCT05191472 · OUTCOME
Proportion of Participants Discontinuing Treatment Due to Toxicity
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- NUMBER
- Unit
- proportion of participants
- Interval / dispersion
- Not reported
- Time frame
- Up to 30 days after discontinuing study treatment, approximately 1 year and 8 months
What was measured
The proportion of participants who reported discontinuing treatment due to a treatment-related toxicity will be reported.
Groups in this outcome
Treatment (Pembrolizumab)
Participants received pembrolizumab IV over 30 minutes on day 1. Cycles repeat every 21 days for up to 2 years in the absence of disease progression or unacceptable toxicity.
| Group | Source count |
|---|---|
| Treatment (Pembrolizumab) | 3 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Treatment (Pembrolizumab) | 0 | Not reported | Not reported | Not reported | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- value
- 0
- denoms
- counts
- group Id
- OG000
- value
- 3
- units
- Participants
- description
- The proportion of participants who reported discontinuing treatment due to a treatment-related toxicity will be reported.
- groups
- description
- Participants received pembrolizumab IV over 30 minutes on day 1. Cycles repeat every 21 days for up to 2 years in the absence of disease progression or unacceptable toxicity.
- id
- OG000
- title
- Treatment (Pembrolizumab)
- param Type
- NUMBER
- reporting Status
- POSTED
- time Frame
- Up to 30 days after discontinuing study treatment, approximately 1 year and 8 months
- title
- Proportion of Participants Discontinuing Treatment Due to Toxicity
- type
- SECONDARY
- unit Of Measure
- proportion of participants
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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