NCT03361748 · OUTCOME
Number of Participants With Safety Related Events
Efficacy and Safety Study of bb2121 in Subjects With Relapsed and Refractory Multiple Myeloma · Source last updated 2025-05-23
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 screening to the end of follow up (approximately 5 years and 2 months)
What was measured
Number of participants with adverse events (AEs), adverse events of special interest (AESI), serious adverse events (SAEs), cytokine release syndrome, neurotoxicity, infection and clinically signifcant laboratory abnormalities.
Analysis population: All Treated Participants
Groups in this outcome
Group identifiers and denominators belong to this outcome only. They may differ in another outcome or in safety reporting.
Analysis denominator · Participants
| Group | Source count |
|---|
| BB2121 | 137 |
|---|
Reported measurements
Any Grade AE
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| BB2121 | 137 | Not reported | Not reported | Not reported | Not reported |
|---|
Grade 3 or 4 AE
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| BB2121 | 136 | Not reported | Not reported | Not reported | Not reported |
|---|
SAEs
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| BB2121 | 98 | Not reported | Not reported | Not reported | Not reported |
|---|
AEs of Special Interest
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| BB2121 | 136 | Not reported | Not reported | Not reported | Not reported |
|---|
Cytokine Release Syndrome
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| BB2121 | 116 | Not reported | Not reported | Not reported | Not reported |
|---|
Neurotoxicity
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| BB2121 | 53 | Not reported | Not reported | Not reported | Not reported |
|---|
Infections
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| BB2121 | 95 | Not reported | Not reported | Not reported | Not reported |
|---|
Clinically Significant Laboratory Abnormalities
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| BB2121 | 0 | Not reported | Not reported | Not reported | Not reported |
|---|
Complete source fields
- classes
- title
- Any Grade AE
- title
- Grade 3 or 4 AE
- title
- SAEs
- title
- AEs of Special Interest
- title
- Cytokine Release Syndrome
- title
- Neurotoxicity
- title
- Infections
- title
- Clinically Significant Laboratory Abnormalities
- description
- Number of participants with adverse events (AEs), adverse events of special interest (AESI), serious adverse events (SAEs), cytokine release syndrome, neurotoxicity, infection and clinically signifcant laboratory abnormalities.
- groups
- description
- BB2121
- id
- OG000
- title
- BB2121
- param Type
- COUNT_OF_PARTICIPANTS
- population Description
- All Treated Participants
- reporting Status
- POSTED
- time Frame
- From screening to the end of follow up (approximately 5 years and 2 months)
- title
- Number of Participants With Safety Related Events
- type
- SECONDARY
- unit Of Measure
- Participants
Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0
Preserved source evidence · Not medical advice