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1 velop live, attenuated HAV vaccines that can be administered orally.
2 erest in developing small molecules that can be administered orally.
3 t hydrolysed by endogenous proteases and may be administered orally.
4 reatment with succimer, a lead chelator that is administered orally.
5 , large volumes of enteric contrast material are administered orally.
6  mg/kg), a glycogen phosphorylase inhibitor, was administered orally.
7 ample, 2.0 umol [14,15]-13C2-retinyl acetate was administered orally.
8                                    All drugs were administered orally.
9                           Both drug regimens were administered orally.
10 diesel/biodiesel fuel blend (80:20 v/v, B20) were administered orally.
11                                        Drugs were administered orally.
12 potecan CNS penetration, 200 mg/kg gefitinib was administered orally 1 hour before 4 mg/kg topotecan
13               Pioglitazone (30 mg/kg weight) was administered orally 1.5 h before and 2 h after the i
14 rvival occurred when 2 x 10(6) corneal cells were administered orally 10 days before orthotopic corne
15                                   Ivosidenib was administered orally (100 mg twice daily to 1,200 mg
16       Two days later, 400 mg of ketoconazole was administered orally 2 hr before to the morning dose.
17                                       Biotin was administered orally (2.1, 8.2, or 81.9 micromol) or
18                                Acalabrutinib was administered orally 200 mg once daily, or 100 mg twi
19 pression of the NGF receptor-IR elements, C3 was administered orally (25 mg/kg, once a day), by gavag
20 or myelodysplastic syndromes (MDS), MGCD0103 was administered orally 3 times weekly without interrupt
21                                          TMZ was administered orally 30 minutes after completion of e
22 eased in diabetic subjects only when glucose was administered orally (37.8 +/- 14.9 vs 68.3 +/- 22.8
23                                    Treatment was administered orally 5 d/wk for 3 months.
24                                        PN401 was administered orally 8 hours after 5-FU administratio
25               Acyclovir or a matched placebo was administered orally, 800 mg five times daily, for 21
26                                   Treatments were administered orally, 801 mg or 399 mg three times a
27           A-988315 (20 or 60 mg/kg) or water was administered orally 90 min before retention testing,
28 lective high-affinity FXR inhibitor that can be administered orally and prevents, or reverses, high-f
29  principal adverse event observed when 2-CdA was administered orally and IV.
30                Peanut or placebo (oat) flour was administered orally and participants and the study t
31                               Contrast media were administered orally and by means of an enema.
32                                    All drugs were administered orally and doses varied by drug combin
33                         Zinc stable isotopes were administered orally and intravenously.
34                            All interventions were administered orally and were given for 3 months aft
35 d murine lymphoid tumors (even when the drug was administered orally) and against human breast and bl
36                   (13)C-glycerol tripalmitin was administered orally as an independent measure of CM
37                                        VP-16 was administered orally as repeated 21-day courses at 50
38 oscine (21 mg/kg), and ondansetron (5 mg/kg) were administered orally as positive controls (PCs).
39 in fixed-dose combination pills; other drugs were administered orally as separate pills.
40                           Immunosuppressants were administered orally as single daily doses.
41                                          RAD was administered orally at 0.5 mg/kg per day for days 0
42                                   Everolimus was administered orally at 10 mg daily and letrozole was
43                                 Zanubrutinib was administered orally at 160 mg twice per day (28-day
44 nistered orally at 10 mg daily and letrozole was administered orally at 2.5 mg daily.
45           During dose escalation, ivosidenib was administered orally at 200-1200 mg daily in 28-day c
46                  Terbutaline (0.2-0.3 mg/kg) was administered orally at 24 and 36 h.
47                                 Lenalidomide was administered orally at 25 mg on days 1 through 21 of
48                                   Marimastat was administered orally at 25, 50, or 100 mg twice daily
49                                  Adavosertib was administered orally at 300 mg once daily on days 1-5
50                                    Sorafenib was administered orally at 400 mg twice daily on a conti
51                                  Ruxolitinib was administered orally at 5 mg twice daily for children
52                                    Alisertib was administered orally at 50 mg twice daily for 7 days
53      During a 24-week core period, mitapivat was administered orally at 50 mg twice daily for the fir
54              Prednisone or a matched placebo was administered orally at 60 mg/d for the first 7 days,
55                                   Everolimus was administered orally at a daily dose of 2.1, 3, 5, or
56                                 Lenalidomide was administered orally at a dose of 25 mg on days 1 to
57                                    Ibrutinib was administered orally at a dose of 560 and 420 mg once
58                                   Lenvatinib was administered orally at a starting dose of 11 mg/m(2)
59          In nonclinical studies, fidaxomicin was administered orally at approximately 1 g/kg/d to dog
60 ither human or nonhuman primate populations, was administered orally at doses ranging from 10(6) to 1
61                                         Drug was administered orally at escalating doses as a solutio
62                                  Quizartinib was administered orally at escalating doses of 12 to 450
63                                  VXA-G1.1-NN was administered orally at three dose levels by prime an
64                                       PT2385 was administered orally at twice-per-day doses of 100 to
65 3C, methyl-2H3]methionine and [2H2]cysteine) were administered orally at 30-min intervals for 8 h.
66 rated virulence attenuation when the strains were administered orally but not when they were administ
67        In groups PROB and LIP/PROB, the PROB was administered orally by addition to the drinking wate
68                                Larotrectinib was administered orally (capsule or liquid formulation),
69 y, the intravenous formulation of irinotecan was administered orally daily for 5 days for 2 consecuti
70                                 Temozolomide was administered orally daily for 5 days, with subsequen
71                                   Ivosidenib was administered orally daily in 28-day cycles.
72                                   Vorinostat was administered orally daily starting at 180 mg/m(2)/d
73                                    Erlotinib was administered orally daily to groups of at least thre
74  mg/kg), a glycogen phosphorylase inhibitor, was administered orally, either alone to create mild hyp
75             Thereafter, 80 mg/kg hydroxyurea was administered orally every 3 days.
76  methionine aminopeptidase type 2 inhibitor, was administered orally every other day at 1, 5, or 10 m
77                 Pravastatin and nicotinamide were administered orally every day for 14 days, starting
78 tive antiviral against SARS-CoV-2 that could be administered orally for use following high-risk expos
79                                   Venetoclax was administered orally for 14 days each cycle.
80                      Citicoline (500 mg/day) was administered orally for 6 weeks, and patients were f
81                                      PSC 833 was administered orally for 7 days, beginning 72 hours b
82           AQX-1125 (450 mg daily) or placebo was administered orally for 7 days.
83    In the present phase 1 study, capravirine was administered orally for up to 28 days to 55 HIV-1-in
84 ice a day (DL1) and 200 mg twice a day (DL2) was administered orally from days 1 to 5 and 8 to 12; al
85 ndothelial cells from relevant donor strains were administered orally from day -14 to day -4 on a dai
86 hat any potential neuroprotective agent must be administered orally, have a safe profile and poses a
87     In addition, we propose that the vaccine be administered orally in a 2-dose schedule, with the fi
88                                    Alisertib was administered orally in 21-day cycles at the recommen
89                                           C3 was administered orally in 5, 10, and 25 mg/kg/day conce
90 th conventional antimicrobial therapy, which was administered orally in 96 percent.
91  fashion via subcutaneous implant, whereas P was administered orally in a cyclic fashion.
92                                   Colchicine was administered orally in a loading dose of 1.5 mg imme
93 ronic disease, a range of doses (0.4-100 mg) was administered orally in a single dose before challeng
94                                  MA 800 mg/d was administered orally in divided doses.
95                                 Olutasidenib was administered orally in doses of 150 mg once daily, 1
96              WAY-202196 or control (vehicle) was administered orally in doses ranging from 1.5 to 50
97                                         SM16 was administered orally in formulated chow.
98             Dasatinib (15 to 240 mg per day) was administered orally in four-week treatment cycles, o
99 ated escalations in the dose of PLX3397 that was administered orally in patients with solid tumors (d
100                                     Nicotine was administered orally in the drinking water to achieve
101                                     Olaparib was administered orally in the form of tablets and given
102                              Both treatments were administered orally in 10 ml (increasing to 20 ml,
103                        When suboptimal doses were administered orally in combination to wild-type mic
104    The NRTI drugs allocated by randomisation were administered orally in fixed-dose combination pills
105  (2.5 mug, 5.0 mug, or 10.0 mug), or placebo were administered orally in two doses 2 weeks apart.
106                                  Arimoclomol was administered orally, in drinking water, from symptom
107                                   Both drugs were administered orally, in tablet formulation.
108              Oseltamivir (GS4104), which can be administered orally, is the prodrug of GS4071, a pote
109 ve a favorable risk-to-benefit ratio when it is administered orally long-term to patients with the pr
110 dehydrogenase, allows fluorouracil (5-FU) to be administered orally on a schedule that simulates cont
111                         Palbociclib 125 mg/d was administered orally on a 21-days-on, 7-days-off sche
112                    Dexamethasone 40 mg daily was administered orally on days 1, 8, 15, and 22 of each
113                                      Therapy was administered orally on the first 5 days of a 28-day
114 xamethasone (20 mg [10 mg if age >75 years]) was administered orally on the same days as bortezomib a
115                                   Both drugs were administered orally on a 3 weeks 'on' and 1 week 'o
116                     Melphalan and prednisone were administered orally on days 1 to 4; carfilzomib was
117                                      Temodar was administered orally once a day for five consecutive
118                         Pirtobrutinib 200 mg was administered orally once a day in 28-day cycles.
119                                        COL-3 was administered orally once daily at one of two doses (
120                                   Ribociclib was administered orally once daily for 16 days after TOT
121     Darapladib 160 mg or placebo monotherapy was administered orally once daily for 3 months, and pat
122               Sunitinib (25, 37.5, or 50 mg) was administered orally once daily on three dosing sched
123                                    Erlotinib was administered orally once daily to cohorts of three t
124                                        COL-3 was administered orally once daily, and doses were escal
125                             Pazopanib 800 mg was administered orally once daily.
126                                       LCL161 was administered orally, once weekly, on a 21-day cycle
127 uires weeks of antibiotic therapy, which can be administered orally or intravenously via a peripheral
128 in that makes use of a unique mechanism, can be administered orally or subcutaneously.
129 solution of diatrizoate meglumine and sodium was administered orally or by means of a nasogastric tub
130                                   Sertraline was administered orally or via nasogastric tube at a dos
131 shown that this novel formulation of AmB can be administered orally, resulting in 99% inhibition of p
132 ificant number (N = 34) of these macrocycles are administered orally, revealing that oral bioavailabi
133                              Both treatments were administered orally starting at 1.0 mg three times
134                               All drug doses were administered orally: sunitinib 50 mg, 4 weeks on an
135                           Dipyridamole 75 mg was administered orally three times daily during the FU
136 dose-escalation phase (n = 47), panobinostat was administered orally thrice weekly every week in comb
137 ntrate derived from pooled donor breast milk was administered orally to 32 healthy adults for 7 days
138                                       STI571 was administered orally to 83 patients with CML in the c
139                                9-cis-Retinal was administered orally to a subset of Rpe65(-/-) mice,
140                           PT150 (900 mg/day) was administered orally to all participants for five day
141      Gefitinib (150, 300, 400, or 500 mg/m2) was administered orally to cohorts of three to six patie
142  mg/kg), a glycogen phosphorylase inhibitor, was administered orally to decrease glucose output in ea
143 eptide synthesized from D-amino acids (D-4F) was administered orally to LDL receptor-null mice on a W
144 Then, to assess its efficacy in vivo, BTKB66 was administered orally to mice for 7 days before subjec
145                                     ARRY-063 was administered orally to ovalbumin (OVA) sensitized an
146                                   Lorlatinib was administered orally to patients at doses ranging fro
147 lective P2X3 and P2X2/3 receptor antagonist, was administered orally to rats and found to produce hig
148  lead that also contained two chlorine atoms was administered orally to rats, and samples of bile, ur
149 lbladder filling, 30 mL of corn oil emulsion were administered orally to all patients followed by dyn
150                               Vector strains were administered orally to germfree mice that were subs
151 ailability was established whereby compounds were administered orally to mice and plasma levels were
152                                The compounds were administered orally to mice with acute T. cruzi inf
153                                     Antigens were administered orally to mice, and antigen-specific g
154 asing doses of egg white or ovomucoid as OIT were administered orally to sensitized mice.
155                 Elacridar and cold erlotinib were administered orally to wild-type (WT) and Abcb1a/b;
156 d once a day on days 1 to 28 and abexinostat was administered orally twice a day on days 1 to 5, 8 to
157                 Patients and Methods MK-8242 was administered orally twice a day on days 1 to 7 in 21
158          During dose escalation, rogaratinib was administered orally twice daily at 50-800 mg in cont
159                                   Lonafarnib was administered orally twice daily at dose levels of 70
160                                    Lapatinib was administered orally twice daily at escalating doses
161  Capecitabine (825, 1,000, or 1,250 mg/m(2)) was administered orally twice daily on days 1 to 14 ever
162 both study groups, 5.0 mg/kg of cyclosporine was administered orally twice daily starting 3 days befo
163 s phase 2 open-label study, 400 mg nilotinib was administered orally twice daily to 280 patients with
164                                       ML120B was administered orally twice daily, either prophylactic
165                                      AZD1775 was administered orally twice per day over 2.5 days per
166 ct (active) and appropriate placebo solution were administered orally twice daily for 12 months, and
167 (acetylcysteine 1200 mg or matching placebo) were administered orally twice daily for 2 doses before
168                     NALL or matching placebo was administered orally two to three times per day, with
169          Ibrutinib at a daily dose of 420 mg was administered orally until disease progression or the
170                                   Belzutifan was administered orally using a 3 + 3 dose-escalation de
171              Allogeneic dendritic cells (DC) were administered orally using a protocol that is known
172    A taste-masked preparation of SNAC 2.25 g was administered orally with heparin 30000 to 150000 IU.
173                          70Zn and dysprosium were administered orally with all meals for 5 consecutiv
174                          Axitinib or placebo were administered orally with food at a starting dose of
175                                 Temozolomide was administered orally within 60 minutes of the end of

 
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