Skip to main content

Table 2 Treatment-emergent adverse events occurring in ≥30% of patients treated with MK-2206 plus trastuzumab ( n = 31)

From: A phase 1 study evaluating the combination of an allosteric AKT inhibitor (MK-2206) and trastuzumab in patients with HER2-positive solid tumors

Adverse event

All grades (%)

Grade 3 (%)

Grade 4 (%)

Fatigue

71.0

0

0

Hyperglycemia

51.8

6.5

0

Rash

58.1

16.7

0

Nausea

48.4

0

0

Alkaline phosphatase increase

45.2

6.5

0

Aspartate aminotransferase increase

45.2

9.7

0

Decreased appetite

41.9

0

0

Diarrhea

35.5

0

0

Alanine aminotransferase increase

32.3

3.2

3.2

Decreased hemoglobin

32.3

3.2

0

Dyspepsia

32.3

0

0

Hypoalbuminenia

32.3

0

0

Vomiting

32.3

0

0