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Table 2 Pharmacokinetic parameters after a single subcutaneous administration of ozoralizumab

From: Efficacy and pharmacokinetics of ozoralizumab, an anti-TNFα NANOBODY® compound, in patients with rheumatoid arthritis: 52-week results from the OHZORA and NATSUZORA trials

Dose (mg)

N

Cmax (μg/mL)

tmax (h)

AUC0-last (h·μg/mL)

AUC0-∞ (h·μg/mL)

t1/2 (day)

CL/F (mL/h)

Vd/F (L)

30

77

4.55 ± 1.18

144 (23.2–336)

2050 ± 523

3280 ± 1280a

18.2 ± 8.21a

10.4 ± 3.91a

5.88 ± 1.72a

80

80

12.5 ± 2.84

144 (22.1–212)

5540 ± 1080

8860 ± 3010

17.9 ± 5.98

9.92 ± 2.93

5.71 ± 1.09

  1. Data are expressed as mean ± standard deviation or median (range)
  2. AUC area under the plasma concentration–time curve, AUC0-∞ AUC from 0 to infinity, AUC0-last AUC from 0 to the last quantifiable data point, CL/F apparent clearance, Cmax maximum concentration, t1/2 elimination half-life, tmax time to maximum concentration, Vd/F apparent volume of distribution
  3. aN = 74