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. 2014 Mar 22;73(5):1031–1039. doi: 10.1007/s00280-014-2438-4

Table 1.

Pharmacokinetic parameters of lenalidomide alone and in the presence of digoxin, quinidine, or temsirolimus

Pharmacokinetic parameter Lenalidomide (10 mg) Lenalidomide (25 mg) Lenalidomide (25 mg)
Alone (n = 17) +Digoxin (n = 17) Alone (n = 14) +Quinidine (n = 14) Alone (n = 17) +Temsirolimus (n = 11)
AUCt (h·ng/mL) 396 (32.7) 386 (38.9) 1,288 (12.1) 1,127 (9.6) 1,276 (12.0) 1,366 (14.5)
AUC (h ng/mL) 475 (23.2) 491 (22.2) 1,361 (12.7) 1,190 (9.8) 1,351 (11.9) 1,445 (14.5)
Cmax (ng/mL) 119 (20.2) 118 (32.8) 367 (26.3) 337 (12.3) 364 (30.0) 361 (24.8)
Tmax (h) 1 (1–2) 1 (1–2) 1 (0.5–3) 1 (0.5–1.5) 0.5 (0.5–2) 1 (1–2)
t1/2 (h) 2.40 (21.0) 2.41 (17.0) 2.81 (10.1) 2.86 (12.9) 2.81 (10.5) 2.69 (9.1)
CLR (mL/min) ND ND 227 (18.3) 245 (11.3) 251 (16.4) 229 (15.6)
fe (% dose) ND ND 74.2 (11.4) 70.2 (6.6) 81.0 (10.0) 79.6 (8.0)

Geometric mean (geometric CV %) data are presented for all parameters except for T max where median (range) data are presented

AUC area under the plasma concentration curve, AUC t, AUC from time zero to the last measurable concentration, AUC AUC from time zero to infinity, CL R renal clearance, C max maximum observed plasma concentration; fe, cumulative urinary excretion as a percentage of administered dose, ND not determined, t 1/2 z terminal-phase half-life, T max time to reach C max