Table 2 Reported toxicity profile during the first course of seliciclib treatment

From: A phase I trial of the selective oral cyclin-dependent kinase inhibitor seliciclib (CYC202; R-Roscovitine), administered twice daily for 7 days every 21 days

 

Seliciclib 100 mg b.i.d

Seliciclib 200 mg b.i.d

Seliciclib 800 mg b.i.d

No. of subjects

3

6

12

No. with grade 3 & 4 adverse events

0

2

7

γ GT increase

0

1

3

Hypokalemia

0

0

3

Hyperglycaemia

0

0

1

Hyponatraemia

0

0

1

Rash

0

0

1

Hypotension

0

0

1

Lymphopenia

0

0

1

Anorexia

0

0

1

Fatigue

0

0

1

ALT increased

0

1

0

AST increased

0

1

0

Alk Phos increase

0

1

0

Bilirubin increase

0

1

0

CKMB increase

0

1

0