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1 currently recommended for adults (twice the intravenous dose).
2 metric mean ratio of the subcutaneous to the intravenous dose.
3 vided doses starting at five times the daily intravenous dose.
4 ion in the tumor was less than 1% of 20mg/kg intravenous dose.
5 micromol/L and 13 400 micromol/L for a 50-g intravenous dose.
6 rmacokinetics were determined after a single intravenous dose.
7 oral voriconazole (VRC) doses are lower than intravenous doses.
8 1 oral dose of HAV was equivalent to 10(4.5) intravenous doses.
9 ieving an MED of 1.5 mg/kg, following weekly intravenous dosing.
10 duced TNF release and shock as compared with intravenous dosing.
11 d the safety and pharmacodynamics of single, intravenous doses (0.025, 0.05, and 0.1 mg/kg) of Hemati
17 esiologist infusing a single, subanesthetic, intravenous dose, and required hospitalization for at le
18 time in tumor tissue, is well-tolerated upon intravenous dosing, and is highly efficacious in the COL
19 lethal Staphylococcus aureus infection after intravenous dosing, and one compound showed protective e
21 re measured after administration of oral and intravenous doses at a dose range of 0.015 to 1.25 g, an
23 ock the LH surge in all animals, whereas all intravenous doses consistently blocked the LH surge.
26 or 7 days (with or without an initial 400-mg intravenous dose) followed by placebo for 7 days (n = 12
28 brain and cerebrospinal fluid after repeated intravenous dosing for up to 4 months in Tg2576 transgen
32 ts (6 PC, 2 BC, and 2 UBC) received a single intravenous dose of (68)Ga-NOTA-AE105 (154 +/- 59 MBq; r
33 ts (6 PC, 2 BC, and 2 UBC) received a single intravenous dose of (68)Ga-NOTA-AE105 (154 +/- 59 MBq; r
39 Patients were treated with O(6)-BG at an intravenous dose of 120 mg/m(2) followed 1 hour later by
40 tructure infections received either a single intravenous dose of 1200 mg of oritavancin or a regimen
44 plasminogen activator (tPA) using a standard intravenous dose of 3.3mg/kg (20% bolus, 80% infused), w
45 lant protein c2 was administered as a single intravenous dose of 30 mug/kg body weight at onset of he
46 a 31% T/C at its solubility-limited maximum intravenous dose of 33 micromol/kg in MDA-MB-435 breast
47 atic malignancies were administered a single intravenous dose of 5 mCi 111In-diethylenetriaminepentaa
48 al resection were each administered a single intravenous dose of 5 mg of isothiocyanatobenzyl diethyl
54 ntidepressant effects resulted from a single intravenous dose of an N-methyl-D-aspartate antagonist.
55 ntidepressant effects resulted from a single intravenous dose of an N-methyl-D-aspartate antagonist;
58 A or Ad5PA and then challenged with a lethal intravenous dose of Bacillus anthracis lethal toxin.
59 ed by measuring changes in blood T2 after an intravenous dose of BMS 180550 were used to determine cl
61 gram, to receive either a single, continuous intravenous dose of brexanolone or placebo for 60 h.
62 atients were recruited and received a single intravenous dose of cefazolin (15 mg/kg) and tobramycin
63 f oral doxycycline, with or without a single intravenous dose of ceftriaxone, or 20 days of oral doxy
67 e sequentially allocated to receive a single intravenous dose of either 0.1, 1, 5, or 10 mg/kg of MRA
68 atment in a randomized fashion with a single intravenous dose of either CDP571 (5 mg/kg) or an equiva
69 > 20, ability to swallow, and </= one single intravenous dose of empiric antibiotic therapy before st
70 5 concomitant with or 4 hours after a single intravenous dose of hemoglobin abolished hemoglobin-indu
73 in rats administered a nontoxic 0.5 mumol/kg intravenous dose of inorganic mercury with or without 2.
78 treated rejection (P=0.035) and lower median intravenous dose of methyl-prednisolone (P=0.017) than N
79 s, which regressed completely after a single intravenous dose of MV-NIS, and in MM1 myeloma xenograft
80 Patients were randomized to receive a single intravenous dose of placebo or an infusion of ibutilide
83 ith magnetic resonance imaging (MRI) that an intravenous dose of protamine labeled with gadolinium ac
84 he kidney and that a single 50- to 200-ng/kg intravenous dose of purified Stx-1 results in thrombocyt
86 ry immune thrombocytopenia received a single intravenous dose of rozrolimupab ranging from 75 to 300
88 -blind, placebo-controlled trial of a single intravenous dose of synthetic human secretin in 60 child
89 00 mg) was administered followed by the same intravenous dose of tacrolimus, and subsequent samples w
90 mouse model of IP, we administered a single intravenous dose of the adeno-associated virus (AAV) vec
91 We assessed the effects of a single 20 mg intravenous dose of the arginine vasopressin receptor 1A
92 Within 90 minutes after receiving a single intravenous dose of the drug, all six volunteers had a s
93 ients with treatment-resistant MDD, a single intravenous dose of the low-trapping NMDA channel blocke
96 ndomly assigned patients to receive a single intravenous dose of ustekinumab (either 130 mg or approx
98 (10-25 mg weekly) were randomized to receive intravenous doses of 10 mg/kg MDX-1100 (n = 35) or place
102 ic monoclonal antibody against TNF-alpha, in intravenous doses of 3 or 10 mg per kilogram of body wei
103 adult patients with HPP received 3 ascending intravenous doses of 5, 10, and 20 mg/kg BPS804, a fully
108 tent of tissue deposition following multiple intravenous doses of gadolinium-based contrast agent (GB
110 the effects of acute administration of small intravenous doses of heroin on rates of glucose utilizat
113 okers received saline followed by escalating intravenous doses of nicotine (0.5 and 1.0 mg/70 kg) giv
115 ynamic contrast enhanced MRI that sequential intravenous doses of protamine in 12 tumor-bearing rats
116 dose (MTD) and safety of single and multiple intravenous doses of PV701 as a single agent in patients
117 kinetics, and antitumor activity of multiple intravenous doses of rhApo2L/TRAIL in patients with adva
118 of trial entry, were recruited to receive 2 intravenous doses of rituximab (1,000 mg), administered
119 hetic baroreflex sensitivity was assessed by intravenous doses of sodium nitroprusside and phenylephr
124 s, with a plasma elimination half-life after intravenous dosing of 4.5 h, oral bioavailability of 77%
125 In subsequent experiments, standard systemic intravenous dosing of stabilized siRNA 72 hours after in
126 Carboplatin was administered as a single intravenous dose once every 21 days at a target area und
128 -5, which was administered as either a 75-mg intravenous dose or a 100-mg subcutaneous dose, or place
129 lprednisolone (1 mg/kg) plus four additional intravenous doses over 24 h, and Group B received intrav
130 ate that PEG-rmMGDF administered as a single intravenous dose potently stimulates platelet production
132 The pharmacokinetic study of DMA at oral and intravenous doses showed its C(max) = 1 hour, bioavailab
133 olae-immunotargeted fluorophores even at low intravenous doses showed rapid and robust pumping across
134 0%) after the 2 largest oral doses and the 1 intravenous dose, suggesting 100% bioavailability of the
135 trations were higher after administration of intravenous doses than after administration of oral dose
136 o be treated 18 hours before craniotomy with intravenous doses that ranged between 40 and 100 mg/m2 g
137 -daily oral doses and 200-300 mg twice-daily intravenous doses, the predicted probabilities of achiev
141 us rituximab and 40 (45%) patients given the intravenous dose, with differences between administratio
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