|
Cohort1: 600 mg lenzilumab
|
| Administration route |
intravenous infusion |
| Donor type |
autologous |
| Pts |
3 |
| Age |
Adult, Older_Adult |
| Lymph depletion |
Yes |
| Adverse reactions |
2/3(All-cause mortality); 2/3(Blood and lymphatic system disorders; Infections and infestations; Metabolism and nutrition disorders; Nervous system disorders; Vascular disorders) |
|
|
Cohort2: 1800 mg lenzilumab
|
| Administration route |
intravenous infusion |
| Donor type |
autologous |
| Pts |
3 |
| Age |
Adult, Older_Adult |
| Lymph depletion |
Yes |
| Adverse reactions |
2/3(All-cause mortality); 3/3(General disorders; Musculoskeletal and connective tissue disorders; Nervous system disorders; Psychiatric disorders) |
|