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1 gnitude and duration of response to therapy (pharmacodynamics).
2 in part B (to assess safety and longer-term pharmacodynamics).
3 exosomes to intercellular drug transfer and pharmacodynamics.
4 ndin exhibiting distinctive pharmacokinetics/pharmacodynamics.
5 y, antitumor efficacy, pharmacokinetics, and pharmacodynamics.
6 acokinetic profile for assessment of in vivo pharmacodynamics.
7 c disturbance per se is unrelated to altered pharmacodynamics.
8 se is related to altered pharmacokinetics or pharmacodynamics.
9 icles provided improved pharmacokinetics and pharmacodynamics.
10 acology of AMG 416 showed readily reversible pharmacodynamics.
11 unds impacting on their pharmacokinetics and pharmacodynamics.
12 ed pharmacokinetics, antitumor activity, and pharmacodynamics.
13 d an overall response, pharmacokinetics, and pharmacodynamics.
14 t of imaging biomarkers to monitor metabolic pharmacodynamics.
15 ing behaviour, indicating dose dependency of pharmacodynamics.
16 itaxel release (extent and rate) and in vivo pharmacodynamics.
17 iability in clopidogrel pharmacokinetics and pharmacodynamics.
18 o enhance active ingredient pharmacology and pharmacodynamics.
19 le of ABCB1 gene in SRL pharmacokinetics and pharmacodynamics.
20 ore a critical step in the prediction of its pharmacodynamics.
21 th antileukemic drug pharmacokinetics and/or pharmacodynamics.
22 owever, this increases the complexity of the pharmacodynamics.
23 ion of the conditions governing the observed pharmacodynamics.
24 micronutrients on drug pharmacokinetics and pharmacodynamics.
25 ule biodistribution, target interactions and pharmacodynamics.
26 nfirm efficacy and further define safety and pharmacodynamics.
27 both intended and unintended, that comprise pharmacodynamics.
28 iable means for quantification of paclitaxel pharmacodynamics.
29 results in great changes in pharmacology and pharmacodynamics.
30 ude understanding of mechanism of action and pharmacodynamics.
31 d improving bacteriocin pharmacokinetics and pharmacodynamics.
32 model accounts for drug pharmacokinetics and pharmacodynamics.
33 recapitulating clinical pharmacokinetics and pharmacodynamics.
34 eir assembly, stability, immunogenicity, and pharmacodynamics.
35 orbidities, and altered pharmacokinetics and pharmacodynamics.
36 for understanding their pharmacokinetics and pharmacodynamics.
37 y and optimizing antibiotic pharmacokinetics/pharmacodynamics.
38 0%), efficacy (45%), pharmacokinetics (28%), pharmacodynamics (23%), and patient enrichment (14%) wer
40 dual variation in anastrozole metabolism and pharmacodynamics among patients treated with the approve
42 ood, Sehgal et al report on the clinical and pharmacodynamics analysis of pomalidomide dosing strateg
43 study was to evaluate the pharmacokinetics, pharmacodynamics and anti-tumour efficacy of the first s
44 murine model that can be used to analyze the pharmacodynamics and antitumor properties of immunostimu
45 evaluates the safety, pharmacokinetics, and pharmacodynamics and defines the recommended phase II do
46 with the compound, including pharmacokinetic/pharmacodynamics and efficacy assessment by TSPO autorad
47 traightforward to relate pharmacokinetics to pharmacodynamics and efficacy by following the time abov
48 tolide field focusing on differentiating the pharmacodynamics and especially the toxicology of the ma
49 riteria for Adverse Events version 4.03, and pharmacodynamics and immunogenicity were also evaluated.
50 ontribute to interactions between cell-based pharmacodynamics and in vivo pharmacokinetics that defin
51 n, FQ plasma and tissue pharmacokinetics and pharmacodynamics and is based on extensive in vitro and
54 t, treatment modification based on patients' pharmacodynamics and pharmacogenomics, and improved supp
55 ase2 inhibitor that possesses both favorable pharmacodynamics and pharmacokinetic (PK) parameters, in
56 ns, and fail to fully capture cytotoxic drug pharmacodynamics and pharmacokinetic variability in obes
57 nd neurodevelopmental delay; however, animal pharmacodynamics and pharmacokinetics do not directly co
60 ate the role of ECMO, including studying the pharmacodynamics and pharmacokinetics of patients receiv
61 , however, little in-depth discussion of the pharmacodynamics and pharmacokinetics of the sedation ag
62 , we examined whether genes important in the pharmacodynamics and pharmacokinetics of these drugs and
63 al drawbacks with such peptides include poor pharmacodynamics and potential scrambling of the disulfi
64 cules within condensates contributes to drug pharmacodynamics and that further understanding of this
66 ion half-life and improved pharmacokinetics, pharmacodynamics, and antitumor activity compared with b
67 ssed safety, tolerability, pharmacokinetics, pharmacodynamics, and antitumor activity of ARN-509 in m
68 and the schedule, safety, pharmacokinetics, pharmacodynamics, and antitumor activity of oral BGJ398,
69 tives were to evaluate the pharmacokinetics, pharmacodynamics, and clinical antitumor activity of var
71 luded safety, tolerability, pharmacokinetics/pharmacodynamics, and efficacy (Disease Activity Score i
72 We assessed the safety, pharmacokinetics, pharmacodynamics, and efficacy of lumacaftor and ivacaft
73 rial, we evaluated the safety, tolerability, pharmacodynamics, and efficacy of lumacaftor/ivacaftor c
74 uate safety, tolerability, pharmacokinetics, pharmacodynamics, and efficacy of LY2439821, a humanized
75 rial evaluated the safety, pharmacokinetics, pharmacodynamics, and efficacy of selinexor (KPT-330), a
78 o characterize the safety, pharmacokinetics, pharmacodynamics, and efficacy, and to identify the reco
83 o inform on different drug pharmacokinetics, pharmacodynamics, and pharmacogenetics in view of the ab
84 dy to evaluate the safety, pharmacokinetics, pharmacodynamics, and potency of i.v. administrations in
85 imum-tolerated dose, pharmacokinetics (PKs), pharmacodynamics, and preliminary antitumor efficacy wer
86 were safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary clinical activity.
87 the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary efficacy of mavorixafo
88 ing drug pharmacokinetics, measuring therapy pharmacodynamics, and providing a marker of therapeutic
89 We determined the safety, pharmacokinetics, pharmacodynamics, and recommended phase II dose of MK-87
90 and to assess its safety, pharmacokinetics, pharmacodynamics, and response rate in individuals with
91 arameters in understanding pharmacokinetics, pharmacodynamics, and toxicities of drugs, but these par
92 tudies of biodistribution, pharmacokinetics, pharmacodynamics, and toxicity as well as scale-up manuf
94 dynamics with antibody pharmacokinetics and pharmacodynamics, and will be generally applicable to fo
95 ndence, during physiologic activity, blocker pharmacodynamics are largely indistinguishable and large
96 SC) administration of nanochelators improves pharmacodynamics, as evidenced by a 7-fold increase in e
97 rations (pharmacokinetics) and drug actions (pharmacodynamics), available data from clinical trials,
98 se of physiologically based pharmacokinetic /pharmacodynamics-based approaches to forward and reverse
102 antimicrobial activity, pharmacokinetics and pharmacodynamics, clinical indications, and safety profi
104 iable biochemical read out of steroidal drug pharmacodynamics could enable a rapid and objective asse
107 24h or continuously worn for 4 days, and the pharmacodynamics effect of changes in the intraocular pr
109 ed understanding of the pharmacokinetics and pharmacodynamics for current and future antimicrobials i
110 ible with live, primary cells and can report pharmacodynamics for drug action on an intended target,
112 ors sought to study the pharmacokinetics and pharmacodynamics for ticagrelor 60 mg compared with 90 m
113 cokinetics, lung tissue pharmacokinetics and pharmacodynamics for two first line anti-TB antibiotics.
115 cell, IC(50,free) = 6.2 nM) and good in vivo pharmacodynamics in a calcium ionophore-stimulated rat m
116 l evaluated apremilast efficacy, safety, and pharmacodynamics in adults with moderate to severe atopi
117 quantification of antibody accumulation and pharmacodynamics in brain tumors, offering a holistic ap
118 netics, safety, and efficacy in children and pharmacodynamics in individuals naive to antiretroviral
126 vel time-series study of drug effects (i.e., pharmacodynamics) is critical for understanding mechanis
128 real-time screening technologies to identify pharmacodynamics/-kinetics of single and combined drugs
130 but differences in underlying aetiology and pharmacodynamics might differentially affect response to
132 gically based computational pharmacokinetics/pharmacodynamics model was constructed to simulate the r
133 e-dose adjustment protocols, pharmacokinetic/pharmacodynamics modeling and international normalizatio
134 Dose-response curves followed exponential pharmacodynamics models for calcium chloride (EC50 1.8 m
137 therapy, however, is limited by the unknown pharmacodynamics of a replicating agent, as well as the
138 study investigated the safety, efficacy, and pharmacodynamics of a selective BTK inhibitor acalabruti
140 PET will be useful for the study of in vivo pharmacodynamics of Abl PKI molecular therapy in humans.
142 safety, tolerability, pharmacokinetics, and pharmacodynamics of AG10 in ATTR-CM patients with sympto
143 on should center on the pharmacokinetics and pharmacodynamics of agents in an attempt to ameliorate p
144 nique insights into the pharmacokinetics and pharmacodynamics of agents that modulate c-Met activity
145 ide unique insight into pharmacokinetics and pharmacodynamics of agents that modulate EGFR activity,
146 factors that affect the pharmacokinetics and pharmacodynamics of anesthetic agents in the obese popul
147 isms in genes related to pharmacokinetics or pharmacodynamics of antileukemic agents, drug metabolism
149 nificant impacts on the pharmacokinetics and pharmacodynamics of artemether-lumefantrine treatment.
150 0263) assessed the safety, tolerability, and pharmacodynamics of ASP4345 in patients with schizophren
152 iminary activity, pharmacokinetics (PK), and pharmacodynamics of BKM120, a potent and highly specific
153 -tolerated dose (MTD), pharmacokinetics, and pharmacodynamics of carfilzomib administered as a 30-min
154 assess the toxicities, pharmacokinetics, and pharmacodynamics of cixutumumab in children to determine
155 or Esomeprazole on the Pharmacokinetics and Pharmacodynamics of Clopidogrel in Healthy Participants:
157 he purpose of this study was to document the pharmacodynamics of CO2 for MBF using prospective end-ti
158 tudies identify a novel process by which the pharmacodynamics of cocaine are derived in vivo, and thu
159 oroestradiol PET imaging would elucidate the pharmacodynamics of combination HDACIs and endocrine the
160 safety, tolerability, pharmacokinetics, and pharmacodynamics of CSL112 in patients with a recent acu
162 is of the antiviral effects, toxicities, and pharmacodynamics of different variants of cardiac glycos
163 irst article describing the pharmacokinetics/pharmacodynamics of doripenem solely in critically ill p
164 udies that describe the pharmacokinetics and pharmacodynamics of drugs in pregnant women are critical
167 designed to assess safety, tolerability, and pharmacodynamics of FBS0701, a novel oral chelator, in a
169 clearance, alters both pharmacokinetics and pharmacodynamics of furosemide in acute kidney injury, a
170 safety, tolerability, pharmacokinetics, and pharmacodynamics of GP2013 plus cyclophosphamide, vincri
171 rapeutic applications aimed at improving the pharmacodynamics of heparin in the treatment of AHR and
172 the safety, efficacy, pharmacokinetics, and pharmacodynamics of ibrutinib (PCI-32765), a first-in-cl
174 safety, tolerability, pharmacokinetics, and pharmacodynamics of iscalimab in healthy subjects and rh
175 e assessed the safety, pharmacokinetics, and pharmacodynamics of ISIS-APO(a)Rx, a second-generation a
176 to assess the safety, pharmacokinetics, and pharmacodynamics of ivacaftor in children aged 2-5 years
177 less, insights into the pharmacokinetics and pharmacodynamics of LAmB continue to evolve and can be u
178 ed dose (MTD), safety, pharmacokinetics, and pharmacodynamics of LCL161 in patients with advanced sol
179 g analysis was done to better understand the pharmacodynamics of Lithium by isolating the norepinephr
183 to Assess the Safety, Pharmacokinetics, and Pharmacodynamics of Multiple Doses of COR-001, NCT028682
185 idine deaminase, on the pharmacokinetics and pharmacodynamics of oral DAC were evaluated in mice and
186 roteins involved in the pharmacokinetics and pharmacodynamics of rasagiline, and genes previously ass
187 safety, tolerability, pharmacokinetics, and pharmacodynamics of recombinant human LCAT (ACP-501).
189 ndary outcomes were the pharmacokinetics and pharmacodynamics of ricolinostat in this combination and
190 acterize the toxicity, pharmacokinetics, and pharmacodynamics of selinexor, a selective inhibitor of
191 taken by analysing the pharmacokinetics and pharmacodynamics of single doses of subcutaneous aldesle
192 efined as the day of injection, and thus the pharmacodynamics of single injections could be assessed;
193 models incorporate the pharmacokinetics and pharmacodynamics of the antibiotics, the innate and adap
194 ed dose (MTD), safety, pharmacokinetics, and pharmacodynamics of the combination in patients with ref
196 nteractions and altered pharmacokinetics and pharmacodynamics of the different antihypertensive medic
197 pairs motor performance concomitant with the pharmacodynamics of the drug, but also impairs future mo
201 mechanisms of action of antibiotics and the pharmacodynamics of their interaction with bacteria tell
206 safety, tolerability, pharmacokinetics, and pharmacodynamics of treatment with JNJ-42165279 in subje
207 mulations and to characterize the safety and pharmacodynamics of triamcinolone acetonide (TA) deliver
208 sed the safety, tolerability, adherence, and pharmacodynamics of two doses of NaHCO(3) over 28 weeks
212 results in altered drug pharmacokinetics and pharmacodynamics or formation of toxic metabolites which
214 of different genetic variants on clopidogrel pharmacodynamics over time in patients undergoing PCI.
216 armacokinetics of GS-9620, and the following pharmacodynamics parameters: interferon-stimulated gene
217 ween plasma pharmacokinetics (PK), tumor PK, pharmacodynamics (PD) (client protein degradation), tumo
219 stemic and mucosal pharmacokinetics (PK) and pharmacodynamics (PD) of 2F5 IgG and 2F5 Fab fragments w
220 ffect of smoking on the pharmacokinetics and pharmacodynamics (PD) of clopidogrel and prasugrel thera
221 se as a whole, and evaluated the single-cell pharmacodynamics (PD) of Ptx (by in vivo PD microscopy).
222 ty, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of rontalizumab, a humanized IgG1
223 ty, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of the human anti-C5 monoclonal an
224 itiating hydroxyurea therapy, to investigate pharmacodynamics (PD) parameters, including HbF response
226 ety and tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and antitumor activity of PF-0056
227 safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and immunogenicity of KRN23 follo
228 evaluated the safety, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary antileukemic acti
229 An understanding of pharmacokinetics (PK), pharmacodynamics (PD), antimicrobial susceptibility test
230 s study evaluated the pharmacokinetics (PK), pharmacodynamics (PD), clinical efficacy and safety of e
231 imum tolerated dose (MTD), pharmacokinetics, pharmacodynamics (PD), efficacy, and safety of duvelisib
232 cogenetics, including pharmacokinetics (PK), pharmacodynamics (PD), gene and pathway interactions, an
234 bes synthesis and stereospecific comparative pharmacodynamics (PD, anticonvulsant activity and terato
235 usceptibility to an antibacterial agent (ie, pharmacodynamics [PD]), is a given; however, drug exposu
237 Analyses of drug pharmacokinetics (PKs) and pharmacodynamics (PDs) performed in animals are often no
238 tment and follow-up and were included in the pharmacodynamics, pharmacokinetics, and safety analyses.
240 the three major pillars of drug development-pharmacodynamics, pharmacokinetics, and toxicity studies
243 sure, determined by the pharmacokinetics and pharmacodynamics (PK/PD) after intravenous (IV) antibiot
245 ategies, such as population pharmacokinetics/pharmacodynamics (PK/PD) and systems biology/pharmacolog
246 -TB) is designed to perform pharmacokinetics/pharmacodynamics (PK/PD) experiments, and hence the desi
247 arge number of tuberculosis pharmacokinetics/pharmacodynamics (PK/PD) studies that have not been subj
250 idered, including viral pharmacokinetics and pharmacodynamics, potential toxic effects, and monitorin
251 bitors can have a beneficial pharmacokinetic/pharmacodynamics profile but are still often avoided due
253 sign of covalent inhibitors with appropriate pharmacodynamics properties coupled with limited unwante
255 tically characterize the pharmacokinetic and pharmacodynamics properties of the SMN splicing modifier
256 lyglutamine-expanded proteins as well as the pharmacodynamics readouts to monitor their efficacy in p
257 to analyze the in vivo pharmacokinetics and pharmacodynamics relationship of KDM1A inhibitors, as ha
258 tered pharmacokinetics (p < 0.01), a reduced pharmacodynamics response to furosemide also became impo
259 aluation Criteria in Solid Tumors) response, pharmacodynamics, RET mutational status, and biomarker a
260 of testing issues, murine and human in vivo pharmacodynamics, safety of off-label doses, and treatme
261 le, we review the clinical pharmacokinetics, pharmacodynamics, safety, and efficacy of LAmB in a wide
262 We evaluated the pharmacokinetics (PKs), pharmacodynamics, safety, and efficacy of selinexor, an
263 l evaluation of ETX0914 pharmacokinetics and pharmacodynamics showed distribution into vascular tissu
264 were estimated through pharmacokinetics and pharmacodynamics simulation, IFE outcome was best predic
265 are not a unidirectional influence on opioid pharmacodynamics, since TLR4(-/-) mice had reduced oxyco
267 al evolution in patients on optimal therapy, pharmacodynamics studies explaining the extraordinarily
268 ry-based timolol release studies and in vivo pharmacodynamics studies in beagle dogs to evaluate the
270 tigation of kinetic mechanisms in disease or pharmacodynamics studies using MS data from longitudinal
271 cokinetic analyses, in vivo pharmacokinetics/pharmacodynamics studies, and maximum-tolerated-dose stu
273 on, including a comparative pharmacokinetics/pharmacodynamics study that is usually conducted in heal
274 ive pathogens include (1) a pharmacokinetics/pharmacodynamics study to evaluate the impact of vancomy
275 rated cellular PTX pharmacokinetics with PTX pharmacodynamics successfully predicted effects of exoso
276 ical data on vancomycin pharmacokinetics and pharmacodynamics suggest a reevaluation of current dosin
278 physical function, frailty, disability, and pharmacodynamics that all merit further investigation.
279 w previously unappreciated complex nonlinear pharmacodynamics that determine their inhibitory potenti
280 of fMRI affords detailed mapping of regional pharmacodynamics that underlie mechanisms of pain suppre
281 orating viral dynamics and pharmacokinetics/ pharmacodynamics to assess how suboptimal adherence affe
282 ing of intratumoral TNP pharmacokinetics and pharmacodynamics to better comprehend their heterogeneou
283 h vein injection, and exhibited the expected pharmacodynamics to remove uric acid in hyperuricemic bl
285 This study evaluated the pharmacokinetics, pharmacodynamics, tolerability, safety, and efficacy of
286 Recent data on polymyxin pharmacokinetics, pharmacodynamics, toxicity, and clinical outcomes sugges
288 -miR, which is more robust than conventional pharmacodynamics using downstream target gene derepressi
291 Combining models of drug pharmacokinetics, pharmacodynamics, viral kinetics and symptom dynamics, w
295 ures and pharmacokinetics were assessed, and pharmacodynamics were measured in blood, hair follicles,
297 , with greatly improved pharmacokinetics and pharmacodynamics when compared with recombinant IL-2 to
298 nt altered indomethacin pharmacokinetics and pharmacodynamics, which is probably the result of reduce
299 the RTB carrier may support distinct in vivo pharmacodynamics with potential to address hard-to-treat
300 edisposition to altered pharmacokinetics and pharmacodynamics with resulting increased risk of toxici