ライフサイエンスコーパス: after administration

1 ects: 20 minutes, 40 minutes, and 70 minutes after administration.

2 PET/CT demonstrated optimal imaging 5-8 d after administration.

3 e incorporation of stable iron isotopes 14 d after administration.

4 olgus monkeys over a time period of 12 weeks after administration.

5 sessment were obtained at 10, 60, and 90 min after administration.

6 draining lymph nodes (LNs) both 3 and 10days after administration.

7 d radiatum of CA3 in ovariectomized mice 6 h after administration.

8 ociated with less vomiting beyond 30 minutes after administration.

9 he prodrug must hydrolyze to its parent drug after administration.

10 nal patient measurements between 5 and 10 wk after administration.

11 orage and potentially during its application after administration.

12 th a near-infrared fluorophore at least 36 h after administration.

13 er administration; activity was greatest 7 h after administration.

14 emiquantitative uptake of (123)I-MIBG at 4 h after administration.

15 , where peak plasma glucose occurs 7 to 8 hr after administration.

16 tes tumors for improved resection on the day after administration.

17 te receptor (NMDAR)-mediated currents 1 week after administration.

18 n of CBDA of 72.7 ng/mL was observed at 14 h after administration.

19 ine metabolites detected in the striatum 1 h after administration.

20 ndrome, which can occur within hours or days after administration.

21 cerns were reported during the 28-day period after administration.

22 nd laser ablation ICP-MS 5, 26, and 52 weeks after administration.

23 2 h and 7.3x and 4.1x, respectively, at 24 h after administration.

24 and asthma symptoms were evaluated 24 weeks after administration.

25 sistent antihyperalgesic effect up to 60 min after administration.

26 rs for vector delivery during the first week after administration.

27 Caffeine enhanced performance 24 h after administration according to an inverted U-shaped d

28 istered BoNT/A1 complex (1 mug) in blood 5 h after administration; activity was greatest 7 h after ad

29 re acquired at approximately 4, 24, and 48 h after administration and analyzed for dosimetry calculat

30 sed on patient imaging during the first week after administration and determination of the activity r

31 stered quickly, and are effective, both soon after administration and for a long duration.

32 in older healthy participants within minutes after administration and for the duration of infusion, w

33 hydroxyvitamin D(3) at 5 minutes and 4 hours after administration, and at 1, 4, 7, 14, 21, 28, 42, an

34 at 20 to 30 minutes and 60 minutes or longer after administration, and neither BP nor HR changed at e

35 study product administration through 7 days after administration, and secondary safety outcomes are

36 opic label abundance in erythrocytes 14 days after administration, and serum hepcidin.

37 ib, (18)F-SKI underwent extensive metabolism after administration, as evidenced by metabolite analysi

38 l uptake of both radiotracers already 10 min after administration but a higher uptake in oral mucosa,

39 nterleukin-6 and Ngal mRNA observed 24 hours after administration but did not affect renal ferroporti

40 nohistochemistry is evident for both at 16 h after administration but not at 15 min or 2 h.

41 onist impaired glucose tolerance immediately after administration but not in the long term.

42 rsistent sirolimus levels in the vessel wall after administration by a coated balloon.

43 es presenting different surface chemistries, after administration by convection-enhanced delivery.

44 inhibited RVP in Brown Norway rats one month after administration compared to neat quininib control (

45 At 1 month after administration for subjects who received 1 treatme

46 r cell targeting and controlled drug release after administration, here we investigated the intratumo

47 oral mucositis pain during the first 4 hours after administration; however, the effect size was less

48 ved CNIR800 reaches maximal levels 4-6 hours after administration in live animals, allowing accurate

49 After administration in mice, DNA from the vaccine could

50 in liver, spleen, brain, and blood 24 hours after administration in mice.

51 are rapidly conveyed to draining lymph nodes after administration in peripheral tissues with programm

52 at 4 years compared with 2.6 (1.6) at 1 year after administration in phase 1 follow-on subjects (n =

53 ulated tissue HO-1 and delivered CO in blood after administration in vivo, supporting their potential

54 ets were significantly enriched in the brain after administration in vivo.

55 Between 180 and 360 min after administration, INI significantly suppressed EGP b

56 on of innate and adaptive immune cells early after administration into mice as compared with control

57 Twenty-four hours after administration, ketamine exerts rapid and robust a

58 At 24 hours after administration, MDA-MB-231 or MCF-7 human breast c

59 ant change in asthma symptoms in the 4 weeks after administration (median change, 0; P = .26, McNemar

60 Vomiting within 30 minutes after administration occurred in 19.3%, 15.6%, and 13.7%

61 ype control rats underwent dynamic PET scans after administration of (11)C-BMP intravenously or by in

62 120 min, 9 time frames) on a PET/CT scanner after administration of (11)C-CURB ( approximately 350 M

63 After administration of (11)C-MeNER, 15 nondemented pati

64 tients who completed at least 3 PET/CT scans after administration of (124)I-MIBG, we estimated the ef

65 ed for 10 min on an integrated PET/MR system after administration of (18)F-FDG or (68)Ga-DOTANOC.

66 The retention of radioactivity in tumors after administration of (64)Cu-ATSM in vivo is substanti

67 The trafficking of (64)Cu in the brain after administration of (64)Cu-GTSM is significantly alt

68 mapping was performed before and >20 minutes after administration of 0.2 mmol/kg of gadobutrol.

69 on and 4 iterative techniques) acquired 30 h after administration of 1 MBq of (124)I.

70 s in ex vivo and in vivo preclinical studies after administration of 1 to rodents, dogs, and monkeys.

71 und in diuresis, and albuminuria was evident after administration of 1% NaCl in drinking water in Npr

72 )I and subsequently underwent imaging 5-10 d after administration of 1-10 GBq of (131)I.

73 After administration of 10 muM S1P, the diameter of affe

74 2, 3, 3.5, 4, 5, 6, 8, 10, 12, and 14 hours after administration of 1000 mg acetaminophen on Days 0

75 1% +/- 9.3% before surgery to 90.5% +/- 3.2% after administration of 1200 mg pancreatin (P < .05); CF

76 PET scans were acquired 60 min after administration of 150-250 MBq of (68)Ga-labeled FA

77 in turn, correlated with radiation response after administration of 2-deoxyglucose, which significan

78 Importantly, after administration of 2-MPA-TG, the concentrations of

79 T-PBV images were acquired before and 1 hour after administration of 20 mg oral sildenafil.

80 y, patients underwent serial PET/CT scanning after administration of 20-40 MBq of (124)I.

81 ging and biodistribution were performed 24 h after administration of 25 mug of (89)Zr-MSB0010853 to m

82 scans were acquired at 10 min, 1 h, and 3 h after administration of 259 +/- 26 MBq of (18)F-FAPI-74.

83 Directly after administration of 3 MBq/kg of FCH, PET imaging was

84 Cardiac PET/CT was performed after administration of 370 MBq of (18)F-FDG.

85 After administration of 3F-NeuAc, liver enzymes in the b

86 a range of 84.6% +/- 3.0% to 90.0% +/- 3.8% after administration of 4-80 mg YLLIP2 (P < .05).

87 in response to SNP was significantly blunted after administration of 400 nm ET-1 (P < 0.05).

88 ment, using a 90-min dynamic PET acquisition after administration of 42.1 +/- 3.9 MBq of (18)F-FMISO

89 pneumococcal carriage and on IPD before and after administration of 7-valent PCV (PCV7) were availab

90 icant therapeutic reduction of thrombus size after administration of 75 U/g body weight scFvSCE5-scuP

91 dure was repeated for the (99m)Tc-DTPA group after administration of 96 MBq (2.6 mCi) of the tracer.

92 Biodistribution at 7 d after administration of [(89)Zr]Zr-DFO-daratumumab showe

93 d and detected by in vivo magnetic resonance after administration of [2-(13) C]-glycine.

94 Compared with standard CT images acquired after administration of a 35% iodinated contrast agent,

95 vels decreases whole-body energy expenditure after administration of a beta3-agonist and reduces beig

96 ernight fasted cohort was scanned before and after administration of a calorie-matched glucose and ex

97 igated coronary MR angiography was performed after administration of a contrast agent in 78 patients

98 e in a time window between 45 and 70 minutes after administration of a dose of 24 international units

99 Fly camera system to detect fluorescent SLNs after administration of a dual-labeled molecular imaging

100 who had acute major bleeding within 18 hours after administration of a factor Xa inhibitor.

101 patterns of responses were observed in vivo after administration of a GnRH agonist.

102 After administration of a low dose of leptin, the durati

103 After administration of a questionnaire, general and ora

104 ge in forced expiratory volume in 1 s (FEV1) after administration of a short-acting bronchodilator ha

105 1)) or forced vital capacity (FVC), or both, after administration of a shortacting beta(2) agonist (1

106 study performed on male Sprague-Dawley rats after administration of a single dose of 5 and 10 mg/kg

107 ma and declining mental status that improved after administration of a single dose of factor eight in

108 erious adverse events (SAEs)--up to 3 months after administration of a single dose of the PsA-TT vacc

109 rapy and restore normal lipoprotein profiles after administration of a single dose.

110 After administration of a single intravenous dose, each

111 n egg yolk and white was measured during and after administration of a SMM/TMP combination in laying

112 9 +/- 0.8 MBq of (89)Zr-cetuximab within 2 h after administration of a therapeutic dose of 500 mg.m(-

113 87 have a 9% risk of developing pancreatitis after administration of a thiopurine, whereas homozygote

114 nalysis were significantly decreased 4 hours after administration of a vascular disrupting agent (VDA

115 hly predictive for the time to relapse, also after administration of adjuvant androgen deprivation th

116 acc-4x (or placebo) were given intradermally after administration of adjuvant.

117 reduced deposition of IgM in the glomerulus after administration of adriamycin and attenuated the de

118 sues from guinea pigs and CFTR knockout mice after administration of alcohol.

119 ccount for around 30% of immediate reactions after administration of amoxicillin-CLV.

120 MR imaging was performed before and after administration of an elastin-specific gadolinium-b

121 n emission tomography and [(11)C]raclopride, after administration of an injection of placebo or 0.5 m

122 oids in samples collected before and 4 weeks after administration of an investigational norovirus vac

123 ace in millimeters squared before and 1 hour after administration of an IV fluid bolus in the emergen

124 evaluated by mapping the R1 relaxation rate after administration of an MRI contrast agent, was signi

125 After administration of anti-CD3 or antigen, with or wit

126 ntriguingly, miR135a levels were upregulated after administration of antidepressants.

127 ks for (re)infection and symptomatic malaria after administration of antimalarial drugs.

128 n each treatment group, the risk of vomiting after administration of any dose of the study agents was

129 trols in an Apc(Min/+) background as well as after administration of AOM and DSS.

130 atients who underwent PET /: CT 24 and 120 h after administration of approximately 25 MBq of (124)I a

131 by (124)I PET/CT at 2, 24, 48, 72, and 96 h after administration of approximately 30-63 MBq of (124)

132 wer, smaller tumors than VP16 (control) mice after administration of azoxymethane and dextran sodium

133 d more inflammation and formed larger tumors after administration of azoxymethane and dextran sulfate

134 MRI data were collected from pregnant mice after administration of b-BSA-Gd-DTPA and analyzed using

135 -Apc (Apc(HET)) mice, which develop adenomas after administration of beta-naphthoflavone, were crosse

136 that only 42 liver genes changed expression after administration of C9 for 4 weeks, suggesting minim

137 Bcl3(-/-) mice developed more severe AP after administration of cerulein or sodium taurocholate

138 -induced metaplasia was investigated in mice after administration of cerulein.

139 fter hepatocyte ablation and HCC development after administration of chemical carcinogens (dimethylbe

140 It also reduces intestinal tumor formation after administration of chemical carcinogens, and in Apc

141 Audiologic testing was completed after administration of cisplatin alone (< 400 mg/m(2);

142 nausea and vomiting in patients with cancer after administration of cisplatin-based highly emetogeni

143 matched expanded cord blood progenitor cells after administration of clofarabine, cytarabine, and gra

144 and at least one time after imaging (>1 day after administration of contrast material).

145 nostic CT at 24 h using a triple-phase delay after administration of contrast; and diagnostic SPECT/C

146 A), and docosahexanoic acid (22:6, DHA) soon after administration of CPB in all cases.

147 ee different stimulus intensities before and after administration of CRF (0.1, 0.3, 1.0, 3.0 or 10.0

148 d proliferation in the neoplastic epithelium after administration of dextran sodium sulfate and azoxy

149 ter oral administration of S Typhimurium and after administration of dextran sodium sulfate compared

150 LL-IL-27 also reduced colitis in mice after administration of dextran sodium sulfate.

151 t1IEC-KO mice, developed more severe colitis after administration of dextran sulfate sodium than cont

152 After administration of dextran sulfate sodium, Tnfsf14(

153 Analysis of uterine mRNAs 24 h after administration of DHT identified significant chang

154 ia length in human chondrocytes in vitro and after administration of dietary lithium to Wistar rats i

155 essenger RNA and studied liver tumorigenesis after administration of diethylnitrosamine and carbon te

156 ainst Anln mRNA developed fewer liver tumors after administration of diethylnitrosamine and carbon te

157 d developed significantly fewer liver tumors after administration of diethylnitrosamine and CCl(4) co

158 ablation of immature DCX-expressing neurons after administration of diphtheria toxin while leaving t

159 bumin-challenged asthmatic mice up to 27days after administration of DNA nanoparticles carrying thymu

160 nt BM volumes and to predict the average ADs after administration of dosimetry-guided (131)I activity

161 R developed less severe colitis and fibrosis after administration of DSS or TNBS, but bone marrow cel

162 erferon-gamma, and T-helper (Th)17 cytokines after administration of DSS, compared with wild-type mic

163 rs (FaDu) and human colorectal tumors (HT29) after administration of either (64)Cu-ATSM or (64)CuCl2.

164 rietal (PAR) cortex were measured before and after administration of either dextromethorphan (NMDA re

165 performed on rhesus monkeys at baseline and after administration of either thiamet-G, a potent OGA i

166 ain uptake of (11)C-erlotinib was not higher after administration of elacridar.

167 gh activity (303.4 MBq +/- 48.1) acquisition after administration of enalaprilat.

168 xpression, but not mice with reduced viremia after administration of entecavir, developed polyfunctio

169 uries were fully reversible after 3-6 months after administration of eribulin, vinorelbine, and ixabe

170 eptor antagonist or ovariectomy but restored after administration of estradiol in ovariectomized mice

171 -/-) mice had reduced inflammatory responses after administration of ethanol or TNBS compared with co

172 ike, jerking movements in mice that improved after administration of ethanol.

173 uring cardiac ablation that rapidly resolved after administration of Factor Eight Inhibitor Bypassing

174 variate, intracranial hypertension increased after administration of fentanyl and/or midazolam (overa

175 as calculated in 15-minute epochs before and after administration of fentanyl and/or midazolam for th

176 No adverse events after administration of ferumoxytol were recorded.

177 who experienced renal failure developed NSF after administration of gadobenate dimeglumine after mor

178 mic fibrosis (NSF), a rare disease occurring after administration of gadolinium-based contrast agents

179 -enhanced gradient-recalled echo MR sequence after administration of gadopentetate dimeglumine was ob

180 were not significantly different before and after administration of Gd-EOB-DTPA.

181 aphy/computed tomography imaging, before and after administration of glucocorticoids.

182 er the anorexigenic effects of GLP-1 release after administration of glutamine.

183 ting cytokines, were significantly decreased after administration of hBD2 in the steroid-sensitive mo

184 subsets, which reached their nadir 4-8 hours after administration of HC.

185 TFAHA accumulation in 9L tumors was observed after administration of HDACs class IIa specific inhibit

186 cranial hypertension increased significantly after administration of high-dose fentanyl (p = 0.02), l

187 d vomiting during the at-risk period (120 h) after administration of highly emetogenic cisplatin-base

188 The appearance of (13)C-bicarbonate signal after administration of hyperpolarized [1-(13)C]pyruvate

189 of dabigatran anticoagulation within 4 hours after administration of idarucizumab as measured by the

190 les were collected before and up to 48 hours after administration of IFN-alpha-2a to measure HCV RNA

191 Protective effects were also observed after administration of IL-17F but not IL-17C or IL-17E.

192 nophils that persist in the blood and airway after administration of IL-5 neutralizing antibodies has

193 ines by these cells, which increased further after administration of IL6.

194 tcomes of stillbirth or spontaneous abortion after administration of influenza vaccine during pregnan

195 After administration of insecticide and fungus, activiti

196 sted Atp7b (-/-) mice exhibited hypoglycemia after administration of insulin due to an impaired gluco

197 c stent in angiographic vasomotor reactivity after administration of intracoronary nitrate.

198 VTA dopamine neurons increases significantly after administration of intragastric sucrose, and deleti

199 CT image of the abdomen acquired 60 seconds after administration of intravenous contrast material (1

200 had a response to induction therapy 8 weeks after administration of intravenous ustekinumab were ran

201 ny) before (baseline) and 1 week and 1 month after administration of intravitreal ranibizumab.

202 ts, we measured hemodynamics at baseline and after administration of iodixanol or iopamidol contrast.

203 e ICa,L current density was decreased by 28% after administration of ISO in TG cardiomyocytes.

204 ording local field potentials in two ferrets after administration of isoflurane in concentrations of

205 ase of CaMKII, which lasted 10 to 20 minutes after administration of ketamine, occurred concurrently

206 ients with cirrhosis, and may further change after administration of lactulose.

207 14%, 95% CI 8.0-21.1] with shedding at day 2 after administration of LAIV) compared with H3N2 (54 of

208 Three days after administration of LDL-TO or sham surgery, the cont

209 lean mice to sweet compounds were increased after administration of leptin antagonist (LA) but not a

210 llowing overnight withdrawal of levodopa and after administration of levodopa.

211 nuclei of rats persists for at least 1 year after administration of linear gadolinium-based contrast

212 fference in the relative uptake measurements after administration of low and high activities (P > .99

213 nt a dual-source, dual-energy CT examination after administration of low-concentration contrast mater

214 tasks (short-term memory) before and 1 hour after administration of low-dose methylene blue or a pla

215 asma eicosanoids transiently increased 3-6 h after administration of LPS.

216 ced in the liver and spleen of Mac-1 KO mice after administration of MDP compared with that of treate

217 nausea and vomiting in patients with cancer after administration of moderately emetogenic chemothera

218 ng during the 5-day (0-120 h) at-risk period after administration of moderately emetogenic chemothera

219 syndrome is the most common serious toxicity after administration of monoclonal antibodies and immune

220 We did a phase 2a trial to assess safety after administration of MSCs to patients with moderate t

221 n by circulating insulin was more pronounced after administration of nasal insulin than after placebo

222 This difference in heart rate dissipated after administration of norepinephrine, and there were n

223 matory manifestations with rapid improvement after administration of off-label, single-dose tocilizum

224 ge injected dose per gram of tissue) 50 days after administration of one gadoteridol dose.

225 In the absence of IRF4 or after administration of oral antibiotics, MHC II(+)CD226

226 the blood glucose level by insulin secretion after administration of oral glucose.

227 sma drug levels of acyclovir can be achieved after administration of oral valacyclovir or intravenous

228 in lesion size of 20% or more 48 to 72 hours after administration of oritavancin.

229 ration of a rescue antibiotic 48 to 72 hours after administration of oritavancin.

230 tolerated with no additional safety signals after administration of oseltamivir.

231 Mice given hgd40 did not develop colitis after administration of oxazolone or 2,4,6-trinitrobenze

232 e and ADAM17 activation in vivo are examined after administration of p40-containing pectin/zein hydro

233 canal were performed successfully before and after administration of pilocarpine, 1%, in 9 healthy ey

234 ng/ml, compared with 18% and 11% of subjects after administration of plain aspirin and PL2200 (p < 0.

235 diabetic mice exhibited increased activation after administration of protease-activated receptor 4 pe

236 ety, tolerability and feasibility before and after administration of proton pump inhibitors.

237 After administration of raclopride and d-amphetamine, th

238 re obtained before and between 0.5 and 120 h after administration of radioiodine.

239 All patients underwent (124)I PET/CT after administration of recombinant human thyroid-stimul

240 Conclusion After administration of relatively large cumulative dose

241 HI reversibility after administration of salbutamol (400 mug) was defined

242 amic (11)C-GSK1482160 PET/CT of mice at 72 h after administration of saline, lipopolysaccharide, or l

243 ivo PET/CT was performed on the mice at 72 h after administration of saline, lipopolysaccharide, or l

244 fter preconditioning, and during and 4 weeks after administration of SER-287 or placebo.

245 declining by ~3-4 log10 in infected patients after administration of single oral doses of DCV.

246 After administration of siRNAs targeting Serpinc1 and Pr

247 red liver cells; levels of Hamp were reduced after administration of small interfering RNAs against P

248 -6, and IL-12p40 are produced in lung tissue after administration of TDM to mice.

249 the "Discrete Whole Report task", 90 trials) after administration of THC (7.5 and/or 15 mg oral) or p

250 p differences at several times post-CSDS and after administration of the antidepressant medication im

251 group of obese and T2DM subjects before and after administration of the antilipolytic drug acipimox

252 afV600E/Pten-driven murine model of melanoma after administration of the B-Raf(V600E) small molecule

253 However, genotype differences emerged after administration of the COMT inhibitor tolcapone: pe

254 respiratory tract infection through 150 days after administration of the dose.

255 bo, and had at least one efficacy assessment after administration of the dose.

256 respiratory tract infection through 150 days after administration of the dose.

257 f the upper airway were performed before and after administration of the DREADD ligand clozapine-N-ox

258 thylene blue vs placebo) and time (before vs after administration of the drug) as factors to assess d

259 The optimal time for imaging after administration of the dual-labeled antibody was 2-

260 We now show that after administration of the first dose of OFA, there was

261 (AUC) for the viral load, which was assessed after administration of the first dose through the 12th

262 lcSph levels in the brains of wild-type mice after administration of the GCase inhibitor conduritol b

263 dynamic (13)C MR spectroscopy were repeated after administration of the glycolytic inhibitor WP1122,

264 session to measure plasma CBD concentrations after administration of the highest CBD dose (800 mg).

265 Drug concentrations peaked about 89-106 h after administration of the highest dose.

266 ter, both collected approximately 4-12 weeks after administration of the last rotavirus vaccine dose.

267 red to larger children and adults (>/=25 kg) after administration of the manufacturers' currently rec

268 Adverse events identified within 1 week after administration of the medication occurred in appro

269 of SCCs and BCCs was observed in 2 patients after administration of the quadrivalent HPV vaccine.

270 scans followed at 30 min, 1 h, 2 h, and 4 h after administration of the radiopharmaceutical.

271 th cocaine at various times (15 min to 48 h) after administration of the selective KOR agonist salvin

272 After administration of the substrate D-luciferin, the l

273 mes and to predict the therapy-delivered ADs after administration of the therapeutic (131)I activity.

274 but the optimal image acquisition time point after administration of the tracer is still under debate

275 Vs delivered systemically to mice before and after administration of the vasopressin V2 receptor anta

276 No obvious disease was observed after administration of this phage in mice.

277 fic PET radiotracer, was measured before and after administration of tiagabine (0.2 mg/kg of body wei

278 as delivered intraperitoneally less than 4 h after administration of trastuzumab (4 mg/kg intravenous

279 veloping unexplained ARF without hypovolemia after administration of vancomycin without coadministrat

280 , we elucidate the human antibody repertoire after administration of vesicular stomatitis virus (VSV)

281 by [(11)C]MADAM PET measurements before and after administration of vortioxetine (0.1-3.0 mg/kg) and

282 n vs. 49.3 IU per kilogram [range, 0 to 376] after administration; P=0.004).

283 tion vs. 0.4 events per year [range, 0 to 4] after administration; P=0.02), as was factor use (mean d

284 miquantitative uptake of (123)I-MIBG at 24 h after administration (r = 0.64, P = 0.04).

285 he protection it confers in the first months after administration remain unknown.

286 c release of the agents at the selected time after administration so that they can reach their intrac

287 At 3, 6, 12, and 24 h after administration, SPECT/CT images were acquired or m

288 I-prolactin were very low, even up to 90 min after administration, the data suggest that CSF is not t

289 pharmacokinetic evaluation of empagliflozin after administration to Egyptian volunteers, and the res

290 s determined in plasma at 20, 50, and 90 min after administration to evaluate the defluorination rate

291 ng agent, which acts within as little as 1 h after administration to mammalian cells to increase NAD(

292 the locations of virions and infected cells after administration to mice of vaccinia virus or Zika v

293 during the last 10-min time frame, 50-60 min after administration) uptake endpoint was sensitive to e

294 kinetics and examined their pharmacokinetics after administration via oral, intraperitoneal, and intr

295 ting the infusion with cessation of bleeding after administration was complete.

296 elocity in first-order arterioles, 5 minutes after administration was zero for these three groups) co

297 toxicity at 8 wk and chronic toxicity at 1 y after administration were evaluated for (225)Ac-L1.

298 induce MAIT cell accumulation in mouse lungs after administration with a co-stimulant.

299 enabled clear tumor visualization on PET 4 h after administration, with a resultant peak tumor-to-liv

300 VRC01 was rapidly absorbed after administration, with peak concentrations 1-6 days