NCT05986682 · OUTCOME
Treatment Characteristics: Dosing Patterns - Dose Reductions During Treatment With BLENREP Therapy
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
- Between baseline and earliest of end of BLENREP treatment, death, lost to contact or end of study timeframe, up to 40 months.
What was measured
Number of participants for whom BLENREP dosing was dose reduced during treatment as categorized by reason.
Groups in this outcome
Multiple Myeloma/Blenrep Participants
Participants with relapsed and/or refractory multiple myeloma who were treated with Belantamab Mafodotin - blmf (BLENREP) in the DCI Oncology outpatient clinics between August 5, 2020 and November 7, 2023
| Group | Source count |
|---|---|
| Multiple Myeloma/Blenrep Participants | 30 |
Reported measurements
Total # of Participants with Dose Reductions for Any Reason
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Multiple Myeloma/Blenrep Participants | 19 | Not reported | Not reported | Not reported | Not reported |
Dose Reduction for Corneal Adverse Event
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Multiple Myeloma/Blenrep Participants | 13 | Not reported | Not reported | Not reported | Not reported |
Dose Reduction for Hematologic Toxicity
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Multiple Myeloma/Blenrep Participants | 6 | Not reported | Not reported | Not reported | Not reported |
Dose Reduction for Other Reason
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Multiple Myeloma/Blenrep Participants | 1 | Not reported | Not reported | Not reported | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- value
- 19
- title
- Total # of Participants with Dose Reductions for Any Reason
- categories
- measurements
- group Id
- OG000
- value
- 13
- title
- Dose Reduction for Corneal Adverse Event
- categories
- measurements
- group Id
- OG000
- value
- 6
- title
- Dose Reduction for Hematologic Toxicity
- categories
- measurements
- group Id
- OG000
- value
- 1
- title
- Dose Reduction for Other Reason
- denoms
- counts
- group Id
- OG000
- value
- 30
- units
- Participants
- description
- Number of participants for whom BLENREP dosing was dose reduced during treatment as categorized by reason.
- groups
- description
- Participants with relapsed and/or refractory multiple myeloma who were treated with Belantamab Mafodotin - blmf (BLENREP) in the DCI Oncology outpatient clinics between August 5, 2020 and November 7, 2023
- id
- OG000
- title
- Multiple Myeloma/Blenrep Participants
- param Type
- COUNT_OF_PARTICIPANTS
- reporting Status
- POSTED
- time Frame
- Between baseline and earliest of end of BLENREP treatment, death, lost to contact or end of study timeframe, up to 40 months.
- title
- Treatment Characteristics: Dosing Patterns - Dose Reductions During Treatment With BLENREP Therapy
- type
- PRIMARY
- unit Of Measure
- Participants
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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