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1 ith placebo and were safe and generally well tolerated.
2 meaningful proportion of patients but poorly tolerated.
3 ned improvements in AD symptoms and was well tolerated.
4 Both dosages were equally effective and well tolerated.
5 360.RESULTSMIC infusions were extremely well tolerated.
6 c antiepileptics, and paracetamol were often tolerated.
7 d its combination with albendazole were well tolerated.
8  vs. 79.7 +/- 7.4%, p = 0.932), but was well tolerated.
9 regardless of age or HIV status and was well tolerated.
10 ment, twice-daily DTG was effective and well tolerated.
11   In RSV-infected infants, JNJ-8678 was well tolerated.
12                             TAK-003 was well tolerated.
13 d M6620 monotherapy, which was safe and well tolerated.
14 he triterpenoid scaffold at carbon-6 are not tolerated.
15               All vaccine regimens were well tolerated.
16                     All injections were well tolerated.
17                    CYP-001 was safe and well tolerated.
18 on of the H3.3K27M-specific vaccine was well tolerated.
19 tion of rhIL-15/anti-PD-L1 was safe and well tolerated.
20                 Cilofexor was generally well-tolerated.
21                Nemolizumab was safe and well tolerated.
22 ve cancers in which oral medications are not tolerated.
23 onnaires indicated that both diets were well tolerated.
24           Results: (18)F-rhPSMA-7.3 was well tolerated.
25   All EBOV GP vaccine formulations were well tolerated.
26                 Treatment was generally well tolerated.
27  virologic response and DAA therapy was well tolerated.
28                            The drug was well tolerated.
29                             IW-3718 was well tolerated.
30 mpared with placebo, and ivosidenib was well tolerated.
31                     AV-101 was safe and well tolerated.
32  intranasal corticosteroids, and it was well tolerated.
33                  Treatment with S/V was well-tolerated.
34        Vaccines were generally safe and well tolerated.
35            Flurpiridaz PET was safe and well tolerated.
36                      rTMS and tDCS were well tolerated.
37 wing and electron-donating substituents were tolerated.
38                               PC786 was well tolerated.
39 b, PCV13, and PPV23 was immunogenic and well tolerated.
40                         Both doses were well tolerated.
41 se and bone metastases and is generally well tolerated.
42                Islatravir was generally well tolerated.
43 e DAA era appears to be efficacious and well tolerated.
44 l therapy with concurrent ibrutinib was well tolerated; 13 patients (68%) received ibrutinib as plann
45 ns of chloroform led to culture GEO12CF that tolerated 83 muM (10 mg.L(-1)) chloroform.
46 vity reaction to vancomycin who successfully tolerated a dalbavancin graded challenge.
47                                 Six subjects tolerated a total of 17 FUS treatments with no adverse e
48                                 The reaction tolerated a wide range of functional groups and heteroar
49 ug-like properties for oral dosing, was well tolerated across preclinical species at pharmacologicall
50                        The estimated maximum tolerated activity was about 1 MBq/kg.
51                          Cenegermin was well tolerated; adverse effects were mostly local, mild, and
52                      The effects of the well-tolerated alkaloid Berberine (BRB), used for treating me
53                         Both TACTs were well tolerated, although early vomiting (within 1 h) was more
54                           Nilotinib was well-tolerated, although more adverse events, particularly mo
55                    Both treatments were well tolerated and adherence during the study was high.
56                          Regadenoson is well tolerated and can be safely used for cardiac MRI stress
57  clinically relevant dose of GS-9688 is well tolerated and can induce a sustained antiviral response
58                 Enasidenib is generally well tolerated and can induce responses in patients with muta
59                            Walnuts were well tolerated and compliance was good.
60 epatitis B virus (HBV) replication, was well tolerated and demonstrated dose-proportional pharmacokin
61                     KAF156 was safe and well tolerated and demonstrated high levels of pre- and post-
62 mpared with vancomycin, fidaxomicin was well tolerated and demonstrated significantly higher rates of
63  and demonstrated that this compound is well tolerated and did not impair normal hematopoiesis in mic
64                     STAR particles were well tolerated and effective at creating micropores when appl
65 vel findings indicate that zolpidem was well tolerated and effective in promoting sleep in people wit
66                          Letermovir was well tolerated and effective in treating CMV-infections in lu
67                          Evolocumab was well tolerated and effectively reduced plasma LDL-C levels in
68                Posaconazole tablets are well tolerated and efficacious in the prophylaxis and treatme
69 us GP vaccine with Matrix-M adjuvant is well tolerated and elicits a robust and persistent immune res
70              Initial data show AB680 is well tolerated and exhibits a pharmacokinetic profile suitabl
71   Conclusion: Ledipasvir-sofosbuvir was well tolerated and highly effective in children 3 to <6 years
72                       All regimens were well tolerated and immunogenic, with trends toward higher ant
73              Ivosidenib monotherapy was well-tolerated and induced durable remissions and transfusion
74  decompensated heart failure (ADHF) was well-tolerated and led to improved outcomes.
75 (PS1) mice, two selected compounds were well tolerated and led to positive trends, albeit statistical
76 5 patients studied, (99m)Tc-PHC-102 was well tolerated and no study drug-related adverse events were
77  IL-2R signaling in Treg cells, but was well tolerated and only gradually impacted Treg cell function
78                Belapectin (2 mg/kg) was well tolerated and produced no safety signals.
79 lotherapy of the left gastric artery is well-tolerated and promotes clinically significant weight los
80           Single-agent EV was generally well tolerated and provided clinically meaningful and durable
81              Cilofexor for 24 weeks was well-tolerated and provided significant reductions in hepatic
82 d that self-sampling with foam swabs is well-tolerated and provides quantitative viral output concord
83                               GB001 was well tolerated and rapidly absorbed with a 14.5-hour terminal
84  repeat dosing indicated that KB105 was well-tolerated and restricted to the dose site.
85 ab in combination with lenalidomide was well tolerated and resulted in a high proportion of patients
86 ccination using the HD-MAP was safe and well tolerated and resulted in immune responses that were sim
87 cted activities used for treatment were well tolerated and resulted in significant tumor growth inhib
88              Oral dosing of PRCL-02 was well tolerated and resulted in suppressed T-cell proliferatio
89 iparum [Pf] sporozoites [SPZ]) has been well tolerated and safe in >1526 malaria-naive and experience
90  antiretroviral regimens were generally well tolerated and showed a distinctive trend of increasing v
91                       Pembrolizumab was well tolerated and showed encouraging antitumour activity in
92 mpared with aflibercept monotherapy, is well tolerated and shows modest anatomic benefit with potenti
93                                R848 was well tolerated and significantly induced IFN-alpha2a, IFN-gam
94 bcutaneous and oral MSA-2 regimens were well tolerated and stimulated interferon-beta secretion in tu
95  range of aromatic aldehydes and ketones are tolerated and successfully converted into the correspond
96                       Acalabrutinib was well tolerated and yielded an overall response rate (ORR) of
97       Extended treatment with VP250 was well tolerated, and desensitization observed at week 52 persi
98 e, and tenofovir alafenamide as a safe, well tolerated, and durable treatment for people with HIV, wi
99 ent vaccine regimen was generally safe, well-tolerated, and found to elicit higher immune responses t
100 ster #7085), we report that ONM-100 was well tolerated, and four solid tumor types could be visualize
101     Novel OPV2 candidates were as safe, well tolerated, and immunogenic as monovalent OPV2 in previou
102   Both novel OPV2 candidates were safe, well tolerated, and immunogenic in children and infants.
103      The C. difficile vaccine was safe, well tolerated, and immunogenic in healthy US adults aged 65-
104                                LSPD was well tolerated, and no complement activation-related pseudoal
105                           Treatment was well tolerated, and no events of hypoglycemia or hypotension
106                     Both protocols were well tolerated, and no severe treatment-related adverse event
107 OPT-302 inhibition of VEGF-C and -D was well tolerated, and OPT-302 combination therapy may overcome
108 plus amodiaquine TACTs are efficacious, well tolerated, and safe treatments of uncomplicated P falcip
109      In addition, alkyl substituents are not tolerated, and the N-H proton of the aniline ring is res
110                    Both treatments were well tolerated, and there were no serious adverse events.
111                          Evolocumab was well tolerated, and treatment-emergent adverse events patient
112 e glucose conjugated compound was far better tolerated, and tumour growth delays for the parent compo
113 nidone, the medical need for a safe and well-tolerated antifibrotic treatment of IPF remains high.
114 CHX) has been described as a possibly better tolerated antimicrobial for ophthalmic procedures.
115         HD-MAP vaccination was safe and well tolerated; any systemic or local adverse events (AEs) we
116      Both Magnets components, which are well-tolerated as protein fusion partners, are photoreceptors
117 ults: Injections of (99m)Tc-ADAPT6 were well tolerated at all mass levels and not associated with adv
118 nd capecitabine, a prodrug of 5-FU, was well tolerated at biologically-active doses.
119 nce and cataplexy while generally being well tolerated at prescribed doses.
120              While a [4Fe-4S] cluster can be tolerated at the AuxI site, the aggregate findings sugge
121 s a safe and painless procedure that is well tolerated because it avoids rectal trauma and patients r
122 However, systemic delivery of R848 is poorly tolerated because of its poor solubility in water and sy
123 bability (TCP) of 99% and, second, a maximal tolerated biologically effective dose (BED(max)) for org
124 ucel-T immunotherapy as maintenance was well tolerated but the primary endpoint was not met.
125              The vaccine was relatively well tolerated, but a high percentage developed a fever >=37.
126           AGS-004 and VOR were safe and well-tolerated, but no substantial impact on RCI was measured
127       Results: (68)Ga-DOTA-Siglec-9 was well tolerated by all subjects.
128 er as well as more beneficial for and better tolerated by at-risk individuals.
129 troduced alleles (RAs) are more likely to be tolerated by modern humans than are introgressed Neander
130                         Desmopressin is well tolerated by most patients, however adverse effects, suc
131 Rs also highlight the types of modifications tolerated by MutY and will guide the development of spec
132 e anti-inflammatory properties, and are well tolerated by the brain, D-serine, an endogenous amino ac
133 Desiccation of plants is often lethal but is tolerated by the majority of seeds and by vegetative tis
134 , in which loss-of-function variants are not tolerated, can be highly successful as targets of inhibi
135 e infusions of ketamine were relatively well tolerated compared to active placebo, except for greater
136 ved progression-free survival and was better tolerated compared with sorafenib in patients with metas
137 an be broadly induced by the clinically well-tolerated compound Quisinostat.
138 al ultrasound, an easily repeatable and well-tolerated diagnostic imaging modality, can address these
139                                  The maximum tolerated dose (MTD) and recommended phase 2 dose (RP2D,
140 ive of phase Ib was to determine the maximum tolerated dose (MTD) for lenvatinib plus pembrolizumab (
141                               At the maximum tolerated dose (MTD) of 400 mug/d, the response rate was
142                             Once the maximum tolerated dose (MTD) was established, 21 patients were t
143 ty, dose-limiting toxicities (DLTs), maximum-tolerated dose (MTD), and preliminary antitumor activity
144 56.8 muM), and low in vivo toxicity (maximum tolerated dose = 150 mg/kg in hamster) as compared with
145 ary objectives were to determine the maximum tolerated dose and dose limiting toxicities of brentuxim
146                                  The maximum tolerated dose and non-tolerated dose were not reached i
147 tor-initiated study was to determine maximum tolerated dose and safety.
148 s the MFIS measured while taking the highest tolerated dose at week 5 of each medication period, anal
149 wever, and whether escalation to the maximum tolerated dose confers clinical benefits that outweigh t
150 sion part, the starting dose was the maximum tolerated dose from the dose-escalation part).
151                                  The maximum tolerated dose of anetumab ravtansine was 6.5 mg/kg once
152                                      Maximum tolerated dose of EV was not established; however, the r
153 logical levels of erythropoietin with a well-tolerated dose of the inducer oligonucleotide.
154 n continuous 28-day cycles until the maximum tolerated dose or recommended phase 2 dose was determine
155 4;11 xenograft tumor model in mice at a well-tolerated dose schedule.
156  1:1 to liraglutide (1.8 mg daily or maximum tolerated dose up to 1.8 mg daily) or placebo plus stand
157          In phase 1, the established maximum tolerated dose was 40 mg of melflufen in combination wit
158                                  The maximum tolerated dose was 400 mg, and the recommended phase 2 d
159                                  The maximum tolerated dose was not reached; 500 mg once per day was
160                                      Maximum tolerated dose was not reached; there were no dose-limit
161           The maximum tolerated dose and non-tolerated dose were not reached in the dose escalation p
162 olerability, the non-tolerated dose, maximum tolerated dose, and recommended phase 2 dose (RP2D).
163 the tolerability, systemic exposure, maximum tolerated dose, and the antitumour activity of nivolumab
164 termine the safety and tolerability, the non-tolerated dose, maximum tolerated dose, and recommended
165               Primary endpoints were maximum tolerated dose, recommended phase 2 dose, and safety in
166 pite receiving statin therapy at the maximum tolerated dose.
167 imary objective was to determine the maximum tolerated dose.
168 primary objective was estimating the maximum tolerated dose; the secondary objectives were to assess
169 n who remained symptomatic despite maximally tolerated doses of GDMT were randomized 1:1 to the Mitra
170 esults of skin test and cellular assays, and tolerated drugs in subsequent pharmacological treatments
171 sy to repeat the study and the study is well tolerated during follow-up.
172 +) secondary MR were randomized to maximally tolerated GDMT plus MitraClip or GDMT alone; 599 had cor
173 n who remained symptomatic despite maximally tolerated GDMT, regardless of prior CRT implantation.
174 ucoma was defined as IOP >21 mmHg on maximum tolerated glaucoma medications or progressive visual fie
175 n who remained symptomatic despite maximally tolerated guideline-directed medical therapy (GDMT).
176 tive suppression of huntingtin was generally tolerated, however high dose AAV5-miHTT did induce astro
177                          Siltuximab was well tolerated; however, adverse events of grade 3 or worse w
178 ed that a variant of AL002c is safe and well tolerated in a first-in-human phase I clinical trial and
179 resumed DR-TB infection is feasible and well tolerated in a high TB burden setting.
180   However, the switch to I438K expression is tolerated in adult mice, sparing normal cells but allowi
181                               PCV20 was well tolerated in adults 60 to 64 years of age, with a safety
182 s kinase 1 inhibitor, was effective and well tolerated in adults with moderate-to-severe atopic derma
183 /- 28 MBq of the radiotracer, which was well tolerated in all patients over a follow-up period of 4 w
184 y demonstrates that (67)Cu-CuSarTATE is well tolerated in BALB/c nude mice and highly efficacious aga
185                                 DSR was well tolerated in both animals and human subjects and produce
186                  Nivolumab was safe and well tolerated in children and young adults and showed clinic
187 ision with amplified centrioles, known to be tolerated in disease states, can occur as part of a norm
188 kably, PHP.eB-iMecp2 administration was well tolerated in female Mecp2 mutant or in wild-type animals
189 ous Ad26,MVA Ebola vaccine regimens are well tolerated in healthy adults, regardless of interval or d
190 ul, durable responses and was generally well tolerated in heavily pretreated patients with relapsed o
191 cate that these candidate compounds are well tolerated in mice without any significant side effects.
192  the analogue and established that 3 is well tolerated in mice, displays substantial PK improvements
193 yed excellent brain penetration and was well-tolerated in mice.
194  the presence of a certain level of rNMPs is tolerated in mitochondrial DNA (mtDNA) although aberrant
195 ophobic substitutions to levels that are not tolerated in monomers.
196                           Treatment was well tolerated in most however serious AEs can occur in those
197 vacamten, a novel myosin inhibitor, was well tolerated in most subjects with symptomatic nHCM.
198              Although OGG1 depletion is well tolerated in non-transformed cells, we report here that
199                 In contrast, type II is well-tolerated in normal monkeys and shows both acute and pro
200         ChAdOx1 nCoV-19 appears to be better tolerated in older adults than in younger adults and has
201  treatment of migraine and was safe and well tolerated in patients for whom multiple previous standar
202 PF-06700841 was generally effective and well tolerated in patients with moderate-to-severe plaque pso
203 y cohort.CONCLUSIONOral NAC is safe and well tolerated in patients with moderately advanced RP and ma
204              In summary, daratumumab is well tolerated in patients with relapsed AL amyloidosis and l
205  of life measures, and it was generally well tolerated in patients with uncontrolled, persistent (pha
206                         BAT product was well tolerated in patients.
207                             ADx-001 was well tolerated in rats and monkeys and exhibited the slow cle
208                    The regimen was also well tolerated in the majority of patients in this older popu
209 targets showed that 2'-5' linkages were well tolerated in the sense strand, but only at a few positio
210                      LAIV appears to be well tolerated in the vast majority of children with asthma o
211                       CHMI was safe and well tolerated in this population.
212                       Overall, MDMA was well-tolerated in this sample.
213 as single or multiple doses is safe and well tolerated in very young infants and is suitable for furt
214                       Debio-1452-NH3 is well tolerated in vivo, reduces bacterial burden in mice and
215  a bioactive anti-inflammatory compound well tolerated in vivo, that shows efficacy in reducing disea
216 ved in vitro profiles, but these were poorly tolerated in vivo.
217        A wide array of alkene substrates are tolerated, including complex drug-like molecules and a t
218 verattenuated, but the 106 PFU dose was well tolerated, infectious (RSV/DeltaNS2/Delta1313/I1314L rep
219 -BEYOND clinical trial (NCT01864798) is well tolerated, inhibits RANK pathway and increases tumor inf
220                Although PI is generally well tolerated, it can be associated with significant ocular
221 ne in patients without rheumatic disease who tolerated LD-MTX during an active run-in period.
222  uncontrolled open-angle glaucoma on maximum tolerated medical therapy.
223 and optic nerve head changes despite maximal tolerated medical therapy.
224 rticles provides a simple, low-cost and well-tolerated method for increasing drug and vaccine deliver
225 gregarious nonhuman primates, eye contact is tolerated more and may be used to communicate other emot
226                           D/C/F/TAF was well tolerated, no participants discontinued due to baseline
227                         Ripretinib is a well-tolerated, novel inhibitor of KIT and PDGFRA mutant kina
228 and electron-releasing substituents are well tolerated on the phthalide core as well as on the aromat
229 t a substantial number of mutations are well tolerated or even enhance ACE2 binding, including at ACE
230                                         Most tolerated oral miltefosine well, with mild gastrointesti
231                  Atogepant was safe and well tolerated over 12 weeks, supporting its phase 3 developm
232               Thus, there is a need for well-tolerated presurgical therapies that could reduce the si
233  for patients who have not benefited from or tolerated previous standard-of-care treatments.
234                     Long-term PGDHi was well-tolerated, reduced the severity of pulmonary fibrotic le
235 stration as well as new, shorter, and better-tolerated regimens.
236 ted human airway organoid cultures, was well tolerated (selectivity index > 7,111) and orally bioavai
237 tion, all doses tested of JNJ-6379 were well tolerated, showed dose-dependent pharmacokinetics, and h
238 low LS BMD, 48 weeks of alendronate was well-tolerated, showed no safety concerns, and significantly
239 year leads to continued response from a well-tolerated, simple-to-use regimen.
240 nib, regorafenib for patients who previously tolerated sorafenib, or ramucirumab (for patients with a
241 ndrome and were on high-intensity or maximum-tolerated statin therapy, with a baseline low-density li
242 erolemia/mixed dyslipidemia taking maximally-tolerated statin therapy.
243 id levels in dyslipidemic PLHIV on maximally-tolerated statin therapy.
244 te coronary syndrome on intensive or maximum-tolerated statin treatment who were randomized to the PC
245  but reveal inherent constraints restricting tolerated substitutions due to epistasis.
246 ast majority of the surface-exposed residues tolerated substitutions without loss of RD3's inhibitory
247 with HIV-1 infection and were generally well tolerated, supporting the further development of islatra
248 However, although being generally far better tolerated than classic cytotoxic chemotherapy, this trea
249 latory activity and that these RAs were more tolerated than NDAs.
250 r dose of ChAdOx1 nCoV-19 is safe and better tolerated than priming doses.
251                           Suicide attempters tolerated the breath-hold and cold-pressor challenges fo
252 ompared with baseline; and 13.5% (19 of 141) tolerated the full double-blind, placebo-controlled food
253                       The non-human primates tolerated the implant without gross pathology or microsc
254                                  All animals tolerated the procedure very well and gained weight with
255                     Although PT2385 was well tolerated, the findings indicate the need for caution in
256                       Highly effective, well-tolerated therapies are now available with markedly simp
257           Six pediatric patients with glioma tolerated this combination without significant adverse e
258 ary analysis, and the PDS generally was well tolerated throughout the entire study period.
259         Oral miltefosine is a generally well-tolerated treatment adjuvant in patients with refractory
260 ipenem/relebactam is an efficacious and well-tolerated treatment option for carbapenem-nonsusceptible
261 sease and nutritional status in patients who tolerated treatment.
262 rs, nitriles, alcohols, and heterocycles are tolerated under the mild conditions.
263 ld type HTT (wtHTT) in Hu21 control mice was tolerated up to 7 months post-injection but may induce i
264 tive transdermal testosterone, although well tolerated, was not more effective than placebo in improv
265                            The procedure was tolerated well in over 100 SHR and normotensive rats tha
266  potent antitumor activity and was very well tolerated when compared to the initial BTC.
267                                8430 was well tolerated when delivered to mice and significantly suppr
268 nt antitumor activity in vivo but was poorly tolerated, which was hypothesized to be the result of un
269 with ROS1 fusion-positive NSCLC, and is well tolerated with a manageable safety profile, making it am
270  fusion-positive solid tumours, and was well tolerated with a manageable safety profile.
271             All treatment regimens were well tolerated with additional exposure.
272            IP RIT (131)I-omburtamab was well tolerated with minimal toxicities.
273                       The treatment was well tolerated with minimal toxicities.
274                           Treatment was well tolerated with no grade 5 treatment-related adverse even
275                              C1-INH was well tolerated with no new safety signals identified in this
276                       All regimens were well tolerated with no serious vaccine-related adverse events
277                         Mavorixafor was well tolerated with no treatment-related serious adverse even
278         Subcutaneous VRC01 was safe and well tolerated with only mild-to-moderate local reactions, pr
279 nstrate that a wide array of substituents is tolerated with this novel scaffold that increased cellul
280                          Remdesivir was well tolerated, with a low incidence of serious adverse event
281                      Both regimens were well tolerated, with a low number of participants reporting a
282         Ivosidenib plus azacitidine was well tolerated, with an expected safety profile consistent wi
283                              The vaccine was tolerated, with induction of neutralizing antibodies and
284 ication of the lipid tail was generally well tolerated, with longer alkyl chains enhancing analogue c
285 h concurrent ibrutinib for R/R CLL were well tolerated, with low CRS severity, and led to high rates
286          Overall, BUP/SAM was generally well tolerated, with most adverse events (AEs) being mild or
287       All doses were generally safe and well tolerated, with no clinically relevant changes in any sa
288   Results: (89)Zr-IAB22M2C infusion was well tolerated, with no immediate or delayed side effects obs
289                  Daratumumab-CyBorD was well tolerated, with no new safety concerns versus the intrav
290                          Infusions were well tolerated, with no participants removed from the study a
291 f AFM13 and pembrolizumab was generally well tolerated, with similar safety profiles compared to the
292                               M6620 was well tolerated, with target engagement and preliminary antitu
293 ative changes at positions 1 and 2 were well-tolerated, with Val(1)-Val(2), Ile(1)-Ala(2), and Leu(1)
294                          Stress CMR was well tolerated without any adverse events.
295 itamin D concentrations were significant and tolerated without developing hypercalcemia.
296                         The vaccine was well tolerated without safety concerns throughout the study.
297                         Both doses were well tolerated without significant changes in BP, weight, or
298            Both regimens were generally well tolerated without unexpected toxicities.
299 y monitoring revealed that the drug was well tolerated, without an increase in plasma triglycerides.
300                          Selatogrel was well tolerated, without major bleeding complications.

 
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