Table 2

Treatment-related AEs occurring in >5% patients or grade ≥3

Treatment-related AE, n (%)Cohort 08 (n=12)Cohort 09 (n=14)Total (N=26)
Grades 1–2Grades 3–4All gradesGrades 1–2Grades 3–4All gradesGrade 1Grade 2Grades 3–4All grades
All AEs11 (91.7)11 (91.7)13 (92.9)1 (7.1)14 (100.0)13 (16.0)11 (42.3)1 (3.8)25 (96.2)
Fever8 (66.7)8 (66.7)11 (78.6)11 (78.6)11 (42.3)8 (30.8)19 (73.1)
Injection site reaction7 (58.3)7 (58.3)9 (62.3)9 (62.3)15 (57.7)1 (3.8)16 (61.5)
Proteinuria6 (50.0)6 (50.0)6 (23.1)6 (23.1)
Neutropenia3 (25.0)3 (25.0)2 (14.3)1 (7.1)3 (21.4)2 (7.7)3 (11.5)1 (3.8)6 (23.1)
Leukopenia3 (25.0)3 (25.0)1 (7.1)1 (7.1)2 (14.3)3 (11.5)1 (3.8)1 (3.8)5 (19.2)
Nausea3 (25.0)3 (25.0)1 (7.1)1 (7.1)4 (15.4)4 (15.4)
Peripheral edema2 (16.7)2 (16.7)2 (14.3)2 (14.3)4 (15.4)4 (15.4)
Vomiting3 (25.0)3 (25.0)1 (7.1)1 (7.1)3 (11.5)1 (3.8)4 (15.4)
Fatigue1 (8.3)1 (8.3)2 (14.3)2 (14.3)3 (11.5)3 (11.5)
Vitiligo1 (8.3)1 (8.3)2 (14.3)2 (14.3)3 (11.5)3 (11.5)
Chills2 (16.7)2 (16.7)1 (7.1)1 (7.1)3 (11.5)3 (11.5)
Pain in extremity3 (25.0)3 (25.0)3 (11.5)3 (11.5)
Rash2 (14.3)2 (14.3)2 (7.7)2 (7.7)
  • AE, adverse event.