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Table 3 Pharmacokinetics of erlotinib after single-dose administration in combination with motesanib

From: Safety and pharmacokinetics of motesanib in combination with gemcitabine and erlotinib for the treatment of solid tumors: a phase 1b study

  

AUC0—24

 

Cmax

Dose Cohort

n

GLSM Ratio

Week 3: Week 2a

(90% CI)

n

GLSM Ratio

Week 3: Week 2a

(90% CI)

50 mg motesanib QD + 100 mg erlotinib QD + gemcitabine

7

0.49 (0.25-0.96)

7

0.65 (0.39-1.08)

100 mg motesanib QD + 100 mg erlotinib QD + gemcitabine

7

0.53 (0.25-1.11)

8

0.82 (0.49-1.37)

125 mg motesanib QD + 100 mg erlotinib QD + gemcitabine

9

0.91 (0.48-1.73)

10

0.73 (0.48-1.09)

75 mg motesanib BID + 100 mg erlotinib QD + gemcitabine

9

0.52 (0.37-0.74)

9

0.75 (0.54-1.05)

100 mg motesanib QD + 150 mg erlotinib QD

7

0.46 (0.34-0.60)

7

0.59 (0.41-0.84)

125 mg motesanib QD + 150 mg erlotinib QD

7

0.46 (0.19-1.13)

7

0.61 (0.50-0.73)

  1. AUC0—24 = area under the curve from time 0-24 h; BID = twice daily; Cmax = peak plasma concentration; CI = confidence interval; GLSM = geometric least squares means; QD = once daily
  2. aWeek 3, erlotinib plus motesanib treatment; week 2, erlotinib treatment only.