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. 2014 Jan 16;110(5):1155–1162. doi: 10.1038/bjc.2013.826

Table 3. Summary of pharmacokinetic analyses for IM and panobinostat.

PK parameter Concentration (ng ml−1) (± s.e.m.) Concentration (±s.e.m.)
Panobinostat Cmax (mean) at 20 mg
D1 12.6 (±3.6) 36.1 nM (±10.3 nM)
D8 16.6 (±2.3) 47.5 nM (±16.6 nM)
D15
15.6 (±3.8)
44.6 nM (±10.9 nM)
IM Cmax (mean): (P=0.185)
2068 (±310) (without pan) 2564 (±190) (with pan)
3.5 μM (±0.5 μM) (without pan) 4.3 μM (±0.3 μM) (with pan)
IM terminal half-life:
20.5 h (with pan)
 
IM trough levels: (mean) (P=0.125) 1085 (±480) (without pan) 1290 (±440) (with pan) 1.8 μM (±0.8 μM) (without pan) 2.2 μM (±0.7 μM) (with pan)