Cohort1: dose level 1
|
Administration route |
infusion |
Dosage |
200 mg, once a week until withdrawn |
Pts |
6 |
Age |
Adult, Older_Adult |
Adverse reactions |
No serious clinical adverse events |
References |
PMID:
27022067
|
|
Cohort2: dose level 2
|
Administration route |
infusion |
Dosage |
400 mg, once a week until withdrawn |
Pts |
7 |
Age |
Adult, Older_Adult |
Adverse reactions |
No serious clinical adverse events |
References |
PMID:
27022067
|
|
Cohort3: dose level 3
|
Administration route |
infusion |
Dosage |
600 mg, once a week until withdrawn |
Pts |
7 |
Age |
Adult, Older_Adult |
Adverse reactions |
1/7(Infusion-related reaction); 1/7(Chills); 1/7(Pruritus); 1/7(Cytokine release syndrome); 1/7(Fatigue); 1/7(Urticaria); 1/7(Cerebral hemorrhage) |
References |
PMID:
27022067
|
|
Cohort4: dose level 4
|
Administration route |
infusion |
Dosage |
800 mg, once a week until withdrawn |
Pts |
8 |
Age |
Adult, Older_Adult |
Adverse reactions |
1/8(Chills); 1/8(Cytokine release syndrome); 1/8(Blood creatinine increased); 1/8(Thrombocytopenia) |
References |
PMID:
27022067
|
|
Cohort5: dose level 5
|
Administration route |
infusion |
Dosage |
1000 mg, once a week until withdrawn |
Pts |
14 |
Age |
Adult, Older_Adult |
Adverse reactions |
1/14(Hypokalemia); 1/14(Electrocardiogram Qt prolonged); 1/14(Oxygen saturation decreased) |
References |
PMID:
27022067
|
|