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1 level of 50 mg/m(2) was determined to be the maximally tolerated dose.
2 was standardized to enalapril 40 mg/d or the maximally tolerated dose.
3 d dose-limiting, with 36 microg/kg being the maximally tolerated dose.
4  three- to fivefold above their conventional maximally tolerated dose.
5 t and during adenosine and dobutamine at the maximally tolerated dose.
6 ion was stopped and 75 micrograms/kg was the maximally tolerated dose.
7 s achieved without dose-limiting toxicity or maximally tolerated dose.
8 ting beta-blockers that may aid in achieving maximally tolerated doses.
9 nude mice when both drugs were used at their maximally tolerated doses.
10 eficient mice in a dose-dependent pattern at maximally tolerated doses.
11 ules of administration argues for the use of maximally tolerated doses.
12 trials should effective biological dose, not maximally tolerated dose, be used to determine phase II
13 , frequent drug administration at lower than maximally tolerated doses can improve activity while red
14 tely 10% mortality and was identified as the maximally tolerated dose in this model.
15  dose level, which defined 800 microg as the maximally tolerated dose in this trial.
16 phase I trial was conducted to determine the maximally tolerated dose (MTD) of concurrent weekly doce
17          Systemic toxicities established the maximally tolerated dose (MTD) of IL-2 as 15 MIU/day.
18                   In this Phase I study, the maximally tolerated doses (MTDs) of i.p. iododeoxyuridin
19 ere enrolled (0.04, 0.15, 0.4 mg), because a maximally tolerated dose of 1.0 mg was identified in a p
20 00 mg/kg per day was comparable to that of a maximally tolerated dose of cyclophosphamide.
21  after at least 10 weeks of treatment with a maximally tolerated dose of paroxetine.
22  a stable antihypertensive regimen including maximally tolerated doses of at least 3 drugs including
23  a stable antihypertensive regimen involving maximally tolerated doses of at least three drugs, inclu
24 atients who had active AAV despite receiving maximally tolerated doses of cyclophosphamide or had con
25 obin level (7.0 to 10.0%) who were receiving maximally tolerated doses of metformin and sulfonylurea
26 h inadequately controlled type 2 diabetes on maximally tolerated doses of metformin, sulphonylurea, o
27 despite treatment for at least 3 months with maximally tolerated doses of three drugs, from 12 second
28 axol could be administered together at their maximally tolerated doses to tumor-bearing mice.
29 any oncology drugs are administered at their maximally tolerated dose without the knowledge of their

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