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1 currently recommended for adults (twice the intravenous dose).
2 rmacokinetics were determined after a single intravenous dose.
3 vided doses starting at five times the daily intravenous dose.
4 metric mean ratio of the subcutaneous to the intravenous dose.
5 ion in the tumor was less than 1% of 20mg/kg intravenous dose.
6 micromol/L and 13 400 micromol/L for a 50-g intravenous dose.
7 1 oral dose of HAV was equivalent to 10(4.5) intravenous doses.
8 oral voriconazole (VRC) doses are lower than intravenous doses.
9 duced TNF release and shock as compared with intravenous dosing.
10 ted with both T. congolense and T. vivax via intravenous dosing.
11 ieving an MED of 1.5 mg/kg, following weekly intravenous dosing.
12 d the safety and pharmacodynamics of single, intravenous doses (0.025, 0.05, and 0.1 mg/kg) of Hemati
17 eliver beta-radiation to tumors via a single intravenous dose (3 or 6 MBq) in mice bearing SK-RC-52 R
19 disease received six cycles every 3 weeks of intravenous, dose-adjusted etoposide, prednisone, vincri
20 esiologist infusing a single, subanesthetic, intravenous dose, and required hospitalization for at le
21 time in tumor tissue, is well-tolerated upon intravenous dosing, and is highly efficacious in the COL
22 lethal Staphylococcus aureus infection after intravenous dosing, and one compound showed protective e
25 re measured after administration of oral and intravenous doses at a dose range of 0.015 to 1.25 g, an
28 ock the LH surge in all animals, whereas all intravenous doses consistently blocked the LH surge.
31 ative urinary d6-alpha-CEHC derived from the intravenous dose excreted over 72 h during the 40% fat (
32 umulative urinary d6-a-CEHC derived from the intravenous dose excreted over 72 h during the 40% fat (
33 or 7 days (with or without an initial 400-mg intravenous dose) followed by placebo for 7 days (n = 12
36 brain and cerebrospinal fluid after repeated intravenous dosing for up to 4 months in Tg2576 transgen
37 , and 15 of every 21-day cycle (group 2); or intravenous dose-fractionated carboplatin (AUC2) and int
38 nous carboplatin (AUC5 or AUC6) on day 1 and intravenous dose-fractionated paclitaxel (80 mg/m(2) by
39 ous dose-fractionated carboplatin (AUC2) and intravenous dose-fractionated paclitaxel (80 mg/m(2) by
40 dose-escalation design, including different intravenous doses (from 5 mg/kg to 30 mg/kg) and interva
43 ical clearance data were generated following intravenous dosing in rats/NHPs and compared to the huma
46 ts (6 PC, 2 BC, and 2 UBC) received a single intravenous dose of (68)Ga-NOTA-AE105 (154 +/- 59 MBq; r
47 ts (6 PC, 2 BC, and 2 UBC) received a single intravenous dose of (68)Ga-NOTA-AE105 (154 +/- 59 MBq; r
48 icipants were randomized 4:4:1 to a one-time intravenous dose of (R)-propafenone, (S)-propafenone, or
55 Patients were treated with O(6)-BG at an intravenous dose of 120 mg/m(2) followed 1 hour later by
56 tructure infections received either a single intravenous dose of 1200 mg of oritavancin or a regimen
60 plasminogen activator (tPA) using a standard intravenous dose of 3.3mg/kg (20% bolus, 80% infused), w
61 lant protein c2 was administered as a single intravenous dose of 30 mug/kg body weight at onset of he
62 umab, n = 169 placebo), and 333 received >=1 intravenous dose of 300 mg vedolizumab (n = 168) or plac
64 a 31% T/C at its solubility-limited maximum intravenous dose of 33 micromol/kg in MDA-MB-435 breast
65 atic malignancies were administered a single intravenous dose of 5 mCi 111In-diethylenetriaminepentaa
66 al resection were each administered a single intravenous dose of 5 mg of isothiocyanatobenzyl diethyl
70 ants, 203 were randomly assigned to a single intravenous dose of 800 mg iron-carboxymaltose and 202 t
72 9(+) lymphoma xenograft model using a single intravenous dose of AAV expressing a secreted version of
79 ntidepressant effects resulted from a single intravenous dose of an N-methyl-D-aspartate antagonist.
80 ntidepressant effects resulted from a single intravenous dose of an N-methyl-D-aspartate antagonist;
83 A or Ad5PA and then challenged with a lethal intravenous dose of Bacillus anthracis lethal toxin.
84 ed by measuring changes in blood T2 after an intravenous dose of BMS 180550 were used to determine cl
86 gram, to receive either a single, continuous intravenous dose of brexanolone or placebo for 60 h.
88 atients were recruited and received a single intravenous dose of cefazolin (15 mg/kg) and tobramycin
89 f oral doxycycline, with or without a single intravenous dose of ceftriaxone, or 20 days of oral doxy
90 ion subjects were randomized 3:1 to a single intravenous dose of ciraparantag (Study 1: 30, 60, or 12
92 ted lipid-lowering therapy received a single intravenous dose of CTX310 (0.1, 0.3, 0.6, 0.7, or 0.8 m
96 e sequentially allocated to receive a single intravenous dose of either 0.1, 1, 5, or 10 mg/kg of MRA
97 atment in a randomized fashion with a single intravenous dose of either CDP571 (5 mg/kg) or an equiva
98 > 20, ability to swallow, and </= one single intravenous dose of empiric antibiotic therapy before st
99 both adult and juvenile Fabry mice, a single intravenous dose of EXG110 achieved supraphysiological p
100 5 concomitant with or 4 hours after a single intravenous dose of hemoglobin abolished hemoglobin-indu
102 en-label, two-part study evaluating a single intravenous dose of HIV-1 bNAbs, PGT121, PGDM1400 and VR
105 in rats administered a nontoxic 0.5 mumol/kg intravenous dose of inorganic mercury with or without 2.
106 e five arms in a 1:1:1:1:1 fashion: a single intravenous dose of ketamine 0.1 mg/kg (n = 18), a singl
112 treated rejection (P=0.035) and lower median intravenous dose of methyl-prednisolone (P=0.017) than N
114 s, which regressed completely after a single intravenous dose of MV-NIS, and in MM1 myeloma xenograft
115 2 copies of SMN2 previously treated with an intravenous dose of onasemnogene abeparvovec in START.
116 e of >=5 were randomized to receive a single intravenous dose of placebo (n = 7 patients) or OP-101 a
117 Patients were randomized to receive a single intravenous dose of placebo or an infusion of ibutilide
119 There were 182 patients receiving standard intravenous dose of PPI, 63 (34.6%) women and 119 (65.4%
121 ith magnetic resonance imaging (MRI) that an intravenous dose of protamine labeled with gadolinium ac
122 he kidney and that a single 50- to 200-ng/kg intravenous dose of purified Stx-1 results in thrombocyt
125 ry immune thrombocytopenia received a single intravenous dose of rozrolimupab ranging from 75 to 300
126 nosed with BCBM and rGBM to receive a single intravenous dose of SG at 10 mg/kg given one day before
127 and at risk of disease progression, a single intravenous dose of sotrovimab, compared with placebo, s
129 -blind, placebo-controlled trial of a single intravenous dose of synthetic human secretin in 60 child
130 00 mg) was administered followed by the same intravenous dose of tacrolimus, and subsequent samples w
131 mouse model of IP, we administered a single intravenous dose of the adeno-associated virus (AAV) vec
132 We assessed the effects of a single 20 mg intravenous dose of the arginine vasopressin receptor 1A
133 Within 90 minutes after receiving a single intravenous dose of the drug, all six volunteers had a s
134 ients with treatment-resistant MDD, a single intravenous dose of the low-trapping NMDA channel blocke
137 rboxymaltose (n = 558) initially given at an intravenous dose of up to 2000 mg that was followed by 5
138 ndomly assigned patients to receive a single intravenous dose of ustekinumab (either 130 mg or approx
142 (10-25 mg weekly) were randomized to receive intravenous doses of 10 mg/kg MDX-1100 (n = 35) or place
146 ic monoclonal antibody against TNF-alpha, in intravenous doses of 3 or 10 mg per kilogram of body wei
147 cokinetic/pharmacodynamic modeling predicted intravenous doses of 3800 mg every 4 weeks would be nece
148 adult patients with HPP received 3 ascending intravenous doses of 5, 10, and 20 mg/kg BPS804, a fully
151 crease in WI rates by giving 2 postoperative intravenous doses of Abx, suggesting postoperative Abx a
157 tent of tissue deposition following multiple intravenous doses of gadolinium-based contrast agent (GB
159 the effects of acute administration of small intravenous doses of heroin on rates of glucose utilizat
164 okers received saline followed by escalating intravenous doses of nicotine (0.5 and 1.0 mg/70 kg) giv
167 ynamic contrast enhanced MRI that sequential intravenous doses of protamine in 12 tumor-bearing rats
168 dose (MTD) and safety of single and multiple intravenous doses of PV701 as a single agent in patients
169 kinetics, and antitumor activity of multiple intravenous doses of rhApo2L/TRAIL in patients with adva
170 of trial entry, were recruited to receive 2 intravenous doses of rituximab (1,000 mg), administered
171 atic solid tumors received escalating weekly intravenous doses of RO7122290 as a single agent (n = 65
172 dpoint of the trial assessed the impact of 6 intravenous doses of RSLV-132 on the mean change from ba
173 hetic baroreflex sensitivity was assessed by intravenous doses of sodium nitroprusside and phenylephr
175 tumours and with a human immune system, high intravenous doses of such a 'switchable T cell nanoengag
180 s, with a plasma elimination half-life after intravenous dosing of 4.5 h, oral bioavailability of 77%
181 We evaluated nonhuman primates following intravenous dosing of AAV8 and AAVrh10 vectors for over
182 cecal ligation and puncture (CLP) procedure, intravenous dosing of AVR-25 (10 mg/kg, 6-12 h post-CLP)
184 In subsequent experiments, standard systemic intravenous dosing of stabilized siRNA 72 hours after in
185 Carboplatin was administered as a single intravenous dose once every 21 days at a target area und
187 -5, which was administered as either a 75-mg intravenous dose or a 100-mg subcutaneous dose, or place
188 Dawley rats received either a single 5 mg/kg intravenous dose or a single 10 mg/kg oral dose of moxif
189 mg) administered postoperatively in a single intravenous dose or to receive 40 mg of enoxaparin admin
191 mly assigned at a 2:1 ratio to receive seven intravenous doses over 10 weeks of AMG 714 (8 mg/kg) or
192 lprednisolone (1 mg/kg) plus four additional intravenous doses over 24 h, and Group B received intrav
193 elbine [oral or intravenous] or gemcitabine [intravenous]; dosing per local label) at 3-weekly or 4-w
194 xplored treatment protocols such as repeated intravenous dosing, personalized patient selection based
195 ate that PEG-rmMGDF administered as a single intravenous dose potently stimulates platelet production
197 The pharmacokinetic study of DMA at oral and intravenous doses showed its C(max) = 1 hour, bioavailab
198 olae-immunotargeted fluorophores even at low intravenous doses showed rapid and robust pumping across
199 0%) after the 2 largest oral doses and the 1 intravenous dose, suggesting 100% bioavailability of the
200 trations were higher after administration of intravenous doses than after administration of oral dose
201 o be treated 18 hours before craniotomy with intravenous doses that ranged between 40 and 100 mg/m2 g
202 -daily oral doses and 200-300 mg twice-daily intravenous doses, the predicted probabilities of achiev
208 us rituximab and 40 (45%) patients given the intravenous dose, with differences between administratio
209 es reveal that rat lungs extract most of the intravenous dose within minutes to achieve precision lun