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Table 2 Adverse events experienced by at least 10% of patients by severity

From: STAT3 antisense oligonucleotide AZD9150 in a subset of patients with heavily pretreated lymphoma: results of a phase 1b trial

AE, n (%)

Total (N = 30)

Grade 1

Grade 2

Grades 3 and 4

Any AE, highest grade experienceda

29 (97)

2 (7)

8 (27)

18 (60)

ALT elevation

12 (40)

5 (17)

5 (17)

2 (7)

AST elevation

12 (40)

7 (23)

4 (13)

1 (3)

Fatigue

11 (37)

4 (13)

5 (17)

2 (7)

Thrombocytopenia

9 (30)

2 (7)

2 (7)

5 (17)

Nausea

6 (20)

2 (7)

3 (10)

1 (3)

Anemia

5 (17)

2 (7)

2 (7)

1 (3)

Hypomagnesemia

5 (17)

5 (17)

0

0

Peripheral edema

5 (17)

3 (10)

2 (7)

0

Alkaline phosphatase elevation

4 (13)

3 (10)

1 (3)

0

Dysphagia

4 (13)

3 (10)

0

1 (3)

Dyspnea

4 (13)

2 (7)

2 (7)

0

Hypercalcemia

4 (13)

1 (3)

2 (7)

1 (3)

Hypokalemia

4 (13)

3 (10)

0

1 (3)

Hyponatremia

4 (13)

3 (10)

0

1 (3)

Neutropenia

4 (13)

1 (3)

0

3 (10)

Vomiting

4 (13)

4 (13)

0

0

Abdominal pain

3 (10)

1 (3)

2 (7)

0

Anorexia

3 (10)

1 (3)

2 (7)

0

Asthenia

3 (10)

1 (3)

1 (3)

1 (3)

Constipation

3 (10)

3 (10)

0

0

Creatinine elevated

3 (10)

2 (7)

1 (3)

0

Diarrhea

3 (10)

3 (10)

0

0

Upper respiratory tract infection

3 (10)

1 (3)

2 (7)

0

Urinary tract infection

3 (10)

1 (3)

2 (7)

0

  1. Abbreviations: AE adverse event, AST aspartate transaminase, ALT alanine transaminase
  2. aIncludes one patient who died of acute respiratory failure (Grade 5 AE) unrelated to the study medication while on trial