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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
39 were evaluable for both pharmacokinetics and pharmacodynamics (50%).
40 dual variation in anastrozole metabolism and pharmacodynamics among patients treated with the approve
41          Differences in pharmacokinetics and pharmacodynamics among statins lead to diverse biologica
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
52 d multiple drug interactions that affect its pharmacodynamics and metabolism.
53                        Assessment of safety, pharmacodynamics and nasal allergic reactivity following
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
58                              We explored the pharmacodynamics and pharmacokinetics in a rabbit model.
59           However, improvement of the drug's pharmacodynamics and pharmacokinetics is desirable.
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
65                We emphasize the diversity in pharmacodynamics and toxicity of the macrolides and keto
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
70 ely estimating the correct pharmacokinetics, pharmacodynamics, and drug interaction effects.
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
76                We assessed pharmacokinetics, pharmacodynamics, and efficacy of the pan-PI3K inhibitor
77  part B (to assess safety, pharmacokinetics, pharmacodynamics, and efficacy).
78 o characterize the safety, pharmacokinetics, pharmacodynamics, and efficacy, and to identify the reco
79 ounds with improved selectivity, appropriate pharmacodynamics, and efficacy.
80 CV viral kinetics, IFN pharmacokinetics, IFN pharmacodynamics, and gene expression profiles.
81  to preliminarily assess antitumor activity, pharmacodynamics, and immunologic correlates.
82 cidence of adverse events, pharmacokinetics, pharmacodynamics, and overall response rate.
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
93              To investigate BBB penetration, pharmacodynamics, and tumor retention kinetics of an ago
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
99 acokinetics (ABCG2, AHR, POR and CYP1A2) and pharmacodynamics (BDNF and SLC6A4) of caffeine.
100 employ conservative designs that incorporate pharmacodynamics/biomarker monitoring.
101      Sex differences in pharmacokinetics and pharmacodynamics characterize many drugs and contribute
102 antimicrobial activity, pharmacokinetics and pharmacodynamics, clinical indications, and safety profi
103                       Our aim was to examine pharmacodynamics (colonic transit, bowel function) and p
104 iable biochemical read out of steroidal drug pharmacodynamics could enable a rapid and objective asse
105                             Pharmacokinetics-pharmacodynamics data show a steady-state concentration
106                         The pharmacokinetics/pharmacodynamics data were used to identify model parame
107 24h or continuously worn for 4 days, and the pharmacodynamics effect of changes in the intraocular pr
108 developed a computational model of cisplatin pharmacodynamics following EBUS-TBNI.
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,
111                                           As pharmacodynamics for the approved dose are optimized onl
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.
114                           Indications of CPT pharmacodynamics from tumor biomarkers such as carbonic
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
119 ing alterations in drug pharmacokinetics and pharmacodynamics in intensive care unit patients.
120                                  We examined pharmacodynamics in the tg2576 APPtg mouse with the prio
121 or activity; exploratory objectives included pharmacodynamics in timed paired tumor biopsies.
122  showed because of a better pharmacokinetics/pharmacodynamics index.
123                                     However, pharmacodynamics indicated a sustained mean occupancy of
124 d uptake of siRNA into the cell and improved pharmacodynamics inside the cell.
125 ween lipid structure/configuration and siRNA pharmacodynamics is unclear.
126 vel time-series study of drug effects (i.e., pharmacodynamics) is critical for understanding mechanis
127           Despite indistinguishable synaptic pharmacodynamics, ketamine provided significantly greate
128 real-time screening technologies to identify pharmacodynamics/-kinetics of single and combined drugs
129 rum pharmacokinetics (HVTN 104) and in vitro pharmacodynamics (LANL CATNAP database).
130  but differences in underlying aetiology and pharmacodynamics might differentially affect response to
131           The computational pharmacokinetics/pharmacodynamics model can be generalized to predict who
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
135  risk for suboptimal drug concentrations and pharmacodynamics must be considered.
136              This study aims to describe the pharmacodynamics of a fluid challenge over a 10-minute p
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
139 significant role in the pharmacokinetics and pharmacodynamics of a variety of drugs.
140  PET will be useful for the study of in vivo pharmacodynamics of Abl PKI molecular therapy in humans.
141  the safety, efficacy, pharmacokinetics, and pharmacodynamics of acalabrutinib.
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
148                             Pharmacokinetics/pharmacodynamics of antimicrobial agents, differences am
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
151  safety, tolerability, pharmacokinetics, and pharmacodynamics of avoralstat.
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:
156 Is) on the steady-state pharmacokinetics and pharmacodynamics of clopidogrel.
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
161                                          The pharmacodynamics of Cyto-012 and wt BoNT/A have similar
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
165 velop an experimental system to evaluate the pharmacodynamics of dual phage-drug therapy.
166 aluated, as well as the pharmacokinetics and pharmacodynamics of ENB-0040.
167 designed to assess safety, tolerability, and pharmacodynamics of FBS0701, a novel oral chelator, in a
168           We characterized the mechanism and pharmacodynamics of five structurally distinct inhibitor
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
173                                          The pharmacodynamics of inhaled heparin are however transien
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
180                     The pharmacokinetics and pharmacodynamics of lumefantrine, a component of the mos
181            The safety, pharmacokinetics, and pharmacodynamics of MMV390048 support its further develo
182                    This new insight into the pharmacodynamics of mTOR inhibitors in regulation of neu
183  to Assess the Safety, Pharmacokinetics, and Pharmacodynamics of Multiple Doses of COR-001, NCT028682
184 ercellular drug transfer that contributes to pharmacodynamics of neighboring cells.
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).
188  significantly improved pharmacokinetics and pharmacodynamics of repeated mATG administration.
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
195 d to reflect pharmacological action and thus pharmacodynamics of the delivered enzyme.
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
198 te understanding of the pharmacokinetics and pharmacodynamics of the drugs.
199           We review the pharmacokinetics and pharmacodynamics of the pediatric procedural sedation ph
200                   We assessed the safety and pharmacodynamics of the vaccine in patients with coeliac
201  mechanisms of action of antibiotics and the pharmacodynamics of their interaction with bacteria tell
202 emporal tissue pharmacokinetics and in vitro pharmacodynamics of these FQs.
203 ient differences in the pharmacokinetics and pharmacodynamics of these medications.
204 BIO 300 and a reasonable illustration of the pharmacodynamics of this radiation countermeasure.
205                     The pharmacokinetics and pharmacodynamics of ticagrelor 60 mg bid have not been s
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
209 absorption, excretion, pharmacokinetics, and pharmacodynamics of various anticoagulants.
210                                          The pharmacodynamics of voriconazole against wild-type and 3
211 harmacokinetics) and the biological effects (pharmacodynamics) of the chemical on the organism.
212 results in altered drug pharmacokinetics and pharmacodynamics or formation of toxic metabolites which
213                                              Pharmacodynamics outcomes were modeled using a Bayesian
214 of different genetic variants on clopidogrel pharmacodynamics over time in patients undergoing PCI.
215 e used to assess furosemide pharmacokinetics/pharmacodynamics parameters.
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
218         Compound 12 was evaluated in a mouse pharmacodynamics (PD) model and demonstrated a 56% incre
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
225  ET and assess the pharmacokinetics (PK) and pharmacodynamics (PD) profile of OA.
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
233 ion affecting drug pharmacokinetics (PK) and pharmacodynamics (PD).
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
236 rmacokinetics [PK]) and protective efficacy (pharmacodynamics [PD]).
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.
239                       The study assessed the pharmacodynamics, pharmacokinetics, and safety of BMS-66
240  the three major pillars of drug development-pharmacodynamics, pharmacokinetics, and toxicity studies
241                              We assessed the pharmacodynamics, pharmacokinetics, preliminary efficacy
242                               We discuss the pharmacodynamics, pharmacokinetics, toxic effects, and c
243 sure, determined by the pharmacokinetics and pharmacodynamics (PK/PD) after intravenous (IV) antibiot
244                 Here we use pharmacokinetics/pharmacodynamics (PK/PD) analysis to rationally develop
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
248 on was driven by a modified pharmacokinetics-pharmacodynamics (PK/PD)-based dosing approach.
249        To determine the pharmacokinetics and pharmacodynamics (PKPD) of ciprofloxacin prophylaxis in
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
252                In addition, pharmacokinetics/pharmacodynamics profile in serum and lung tissue showed
253 sign of covalent inhibitors with appropriate pharmacodynamics properties coupled with limited unwante
254 ay, in part, be parkin-independent or to the pharmacodynamics properties of nilotinib.
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
266                       Human pharmacokinetics/pharmacodynamics studies confirmed this link between mic
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
269                                  Exploratory pharmacodynamics studies including changes in diffusion-
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
272 ristic drug, SAL, during pharmacokinetic and pharmacodynamics studies.
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
277                                              Pharmacodynamics suggested that a single dose of oritava
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
284          We compare the pharmacokinetics and pharmacodynamics to the clinical comparator progesterone
285   This study evaluated the pharmacokinetics, pharmacodynamics, tolerability, safety, and efficacy of
286   Recent data on polymyxin pharmacokinetics, pharmacodynamics, toxicity, and clinical outcomes sugges
287 macology relies on ligands that change their pharmacodynamics upon photoisomerization.
288 -miR, which is more robust than conventional pharmacodynamics using downstream target gene derepressi
289  formulation is a major factor in optimizing pharmacodynamics using this technique.
290             Clopidogrel pharmacokinetics and pharmacodynamics vary widely despite rigorous exclusion
291   Combining models of drug pharmacokinetics, pharmacodynamics, viral kinetics and symptom dynamics, w
292                                              Pharmacodynamics were assessed by measuring the ability
293                         Pharmacokinetics and pharmacodynamics were assessed on days 9 and 10.
294        Pharmacokinetics, immunogenicity, and pharmacodynamics were evaluated, and disease activity wa
295 ures and pharmacokinetics were assessed, and pharmacodynamics were measured in blood, hair follicles,
296                                 Efficacy and pharmacodynamics were secondary end points.
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

 
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