ライフサイエンスコーパス: daily oral administration

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1 Zucker fatty rats following 1 and 2 weeks of daily oral administration.

2 Daily oral administration of 20g significantly prolonged

3 Once-daily oral administration of 22 for 14 days led to 85% i

4 endent medulloblastoma allograft model after daily oral administration of 40 mg/kg of compound 28.

5 f children at high risk for type 1 diabetes, daily oral administration of 67.5 mg of insulin, compare

6 Moreover, daily oral administration of bardoxolone methyl to monke

7 KLN-205 squamous cell carcinoma mouse model, daily oral administration of EPA resulted in a significa

8 In contrast, daily oral administration of estradiol did not affect ei

9 Once-daily oral administration of inhibitor 9i (AP24226) sign

10 Four weeks of once-daily oral administration of L-FMAU significantly reduce

11 Conversely, daily oral administration of lysozyme prevented expansio

12 Once daily oral administration of MK-869 was effective in red

13 Daily oral administration of NPS 2143 to osteopenic ovar

14 In MDA-MB-231 tumor-bearing mice, daily oral administration of OSU-53 (50 and 100 mg/kg) s

15 We then determined the efficacy of daily oral administration of PD173074 for 28 days in two

16 Daily oral administration of resolvin D1, a downstream m

17 was assessed before, during and after timed daily oral administration of saline vehicle (n=12), rame

18 of abciximab and again after 1 week of twice-daily oral administration of study drug.

19 Daily oral administration of SU11657 at 40 mg/kg suppres

20 s from rats withdrawn for 2 days from 1-week daily oral administration of the benzodiazepine, fluraze

21 Once daily oral administration of this compound at 100 mg/kg

22 drug abuse liability, animals received three daily oral administrations of these doses of MP for up t

23 n vivo model of bone turnover following once-daily oral administration, these two compounds were sele

24 We report here that daily oral administration to mice of the brain-penetrant

25 C59 displayed good bioavailability, as once daily oral administration was sufficient to maintain blo

26 rts to identify a compound suitable for once daily, oral administration with low drug-drug interactio

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