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1 nd a 20-wk open-label extension (OLE) at the maximum dose.
2 ich however was applied at a 50 times higher maximum dose.
3 r soy, and most reactions occurred after the maximum dose.
4 placebo or flexibly dosed pramipexole (mean maximum dose=1.7 mg/day, SD=1.3) added to existing mood
5 eceive intravenous dexamethasone (0.5 mg/kg, maximum dose 10 mg) or saline, every 6 hrs for six doses
6 l of placebo (bid), low-dose MPH (0.3 mg/kg; maximum dose, 10 mg bid), and moderate-dose MPH (0.6 mg/
8 rubicin 50 mg/m(2), vincristine 1.4 mg/m(2) (maximum dose 2 mg), and rituximab 375 mg/m(2) on day 1,
9 andomized to MTX 15 mg/m2 body surface area (maximum dose 20 mg) once a week while continuing on UDCA
12 ioperative dose of dexamethasone (0.5 mg/kg; maximum dose, 20 mg), with an equivalent volume of 0.9%
14 umine [0.1 mmol per kilogram of body weight, maximum dose, 20 mL]) for hepatobiliary indications were
15 and >/= 25 kg) and chewable tablet 6 mg/kg (maximum dose 300 mg) twice daily (2 to <12 years) was we
17 mumab per square meter of body-surface area (maximum dose, 40 mg) subcutaneously every other week for
18 ptomatic myeloma were also treated as above (maximum dose 400 mg) and received dexamethasone 20 mg/m(
19 usion of IdU (200 mg/m(2) body surface area; maximum dose, 400 mg) over a 30-minute period; the IdU h
20 rsus 4.7 mg/day), a longer number of days to maximum dose (5.7 days versus 3.9 days), and a maximum r
21 continue on risperidone if they had a higher maximum dose (5.7 mg/day versus 4.7 mg/day), a longer nu
22 /kg/week), etanercept alone (0.8 mg/kg/week, maximum dose 50 mg), or etanercept plus MTX for 3 years
23 domization to degludec/liraglutide (n = 278; maximum dose, 50 U of degludec/1.8 mg of liraglutide) or
24 , to receive 25% albumin (2 g [8 mL] per kg; maximum dose 750 mL) or the equivalent volume of isotoni
26 tidepressant regimens, received either DHEA (maximum dose = 90 mg/day) or placebo for 6 weeks in a do
28 ntine (maximum dose, 900 mg) plus isoniazid (maximum dose, 900 mg) (3HP-DOT) and 31% for 9 months of
29 f directly observed once-weekly rifapentine (maximum dose, 900 mg) plus isoniazid (maximum dose, 900
30 atment-refractory depression (at least three maximum-dose, adequate-duration medication treatments),
31 atment-refractory depression (at least three maximum-dose, adequate-duration medication treatments),
33 rsensing was observed in 20 of 21 devices at maximum doses and in 17 of 20 devices at typical doses.
34 nstraint; IPSA2, without a constraint on the maximum dose; and IPSA2-0, identical to IPSA2 but withou
36 s of SDI at TL were age, corticosteroid use (maximum dose at T0), number of American College of Rheum
37 to phenotypic or microenvironmental factors; maximum dose density chemotherapy hastens rapid expansio
39 abdomen was 15.12 cGy and 0.97 cGy while the maximum dose for the skin was 17.3 cGy and 1.32 cGy.
41 and a phase II trial of HPV16 L2E7E6 at the maximum dose in 29 women with high-grade anogenital intr
42 tomography: IPSA1, with a constraint on the maximum dose in the target volume; IPSA1-0, identical to
45 5% of the critical structure volume (D(5%)), maximum dose, mean dose, and normal tissue complication
46 longed reduction of WBCs was observed at the maximum dose of (90)Y-anti-CD20 IgG, whereas pretargetin
50 A model was developed that calculates the maximum dose of 131I that may be dispensed to an outpati
51 g, which could be increased, as needed, to a maximum dose of 150 mg daily, for a total of 12 weeks.
56 t an initial dose of 50 mg/d (escalated to a maximum dose of 200 mg/d based on tolerability and respo
58 r day, up-titrated until intolerance or to a maximum dose of 25 mg/kg or 50 mg/kg per day (dependent
65 ightmare response over 6 weeks to a possible maximum dose of 5 mg midmorning and 20 mg at bedtime for
66 doses given on the first day, including the maximum dose of 500 mg peanut flour (cumulative dose, 99
68 ting dose was 2 microg/kg/d and increased to maximum dose of 6 microg/kg/d (average dose, 0.33 mg/d).
69 MAS-ER doses were titrated over 2 weeks to a maximum dose of 60 mg daily, and topiramate doses were t
71 ose of 150 mg per day that was adjusted to a maximum dose of 600 mg per day or matching placebo for u
72 as increased by 200 mg every 2 weeks until a maximum dose of 800 mg or prohibitive toxicity was reach
74 upper GI tract, which was dose-limiting at a maximum dose of 875 mg/m(2) (doxorubicin equivalent, 25
76 iology and Chronic Health Evaluation II, and maximum dose of norepinephrine day 1) (hazard ratio, 2.9
78 h symptoms that were not controlled with the maximum dose of opioid were treated with adjunctive phen
80 hours), inotrope score (calculated from the maximum dose of the individual inotropic agents administ
85 with hypertension (using >/=2 medications at maximum doses or >2 at moderate doses) and a body mass i
90 followed by an extension phase involving the maximum dose that could be administered without adverse
91 increasing the dose of dBG to 300 mg/m2 (the maximum dose that could be delivered i.p. in a standard
94 gs challenge the existing flawed paradigm of maximum dose treatment, a strategy that inevitably produ
96 predefined stabilization criteria after the maximum dose were classified as treatment failure, at wh
97 th charged particles can potentially deliver maximum doses while minimizing irradiation of surroundin
99 mg of liraglutide) or glargine (n = 279; no maximum dose), with twice-weekly titration to a glucose
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