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Table 3 Incidence of CTCAE Grade 3 and 4 adverse events (occurring in ≥ 2 patients), regardless of causality

From: A first in human, safety, pharmacokinetics, and clinical activity phase I study of once weekly administration of the Hsp90 inhibitor ganetespib (STA-9090) in patients with solid malignancies

 

Number (%) of patients*

 

Ganetespib

Ganetespib

Ganetespib

All

7-114 mg/m2

150-216 mg/m2

259 mg/m2

patients

n = 25 (%)

n = 22 (%)

n = 6 (%)

n = 53 (%)

Any event

17 (68)

14 (63.6)

5 (83.3)

36 (67.9)

Fatigue†

1 (4)

4 (18.2)

1 (16.7)

6 (11.3)

Asthenia†

1 (4)

1 (4.5)

2 (33.3)

4 (7.5)

Diarrhea †

1 (4)

2 (9.1)

1 (16.7)

4 (7.5)

Hypophosphatemia

2 (8)

2 (9.1)

0

4 (7.5)

ALT elevation†

2 (8)

1 (4.5)

0

3 (5.7)

Dehydration

1 (4)

1 (4.5)

1 (16.7)

3 (5.7)

Hyperbilirubinemia

1 (4)

2 (9.1)

0

3 (5.7)

Hyponatremia

3 (12)

0

0

3 (5.7)

Arthralgia

1 (4)

0

1 (16.7)

2 (3.8)

Serum amylase elevated†

1 (4)

1 (4.5)

0

2 (3.8)

Hypokalemia†

0

2 (9.1)

0

2 (3.8)

Spinal cord compression

2 (8)

0

0

2 (3.8)

  1. *A patient may have had more than one event.
  2. †Considered by the investigator to be clinically significant.