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Table 3 Pharmacokinetic parameters in human following single oral doses of MIV-711

From: Nonclinical and clinical pharmacological characterization of the potent and selective cathepsin K inhibitor MIV-711

Dose (mg)

Cmax (µmol/L)

AUC0–t (µmol/L × h)

AUCinf (µmol/L × h)

t½ (h)

t amax (h)

Cmax/dose

n

20

0.033 (36)

0.128 (36)

0.158 (32)

3.4 (13)

1.0 (0.50–2.0)

0.12 (26)

7

100

0.293 (35)

1.13 (38)

1.17 (37)

3.7 (15)

1.0 (1.0–2.2)

0.21 (23)

7

200

0.756 (43)

2.45 (36)

2.51 (35)

5.0 (16)

1.0 (0.50–1.0)

0.27 (36)

7

400

1.18 (43)

4.62 (33)

4.75 (32)

6.5 (44)

1.0 (1.0–1.5)

0.23 (37)

7

600

1.39 (37)

6.75 (30)

6.89 (30)

8.3 (34)

1.0 (1.0–3.0)

0.17 (38)

7

  1. Data are presented as geometric mean (CV%)
  2. aMedian (min–max)