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NO_PRETOX_REL | Each cycle consisted of 3 consecutive days of dosing followed by a 4 - day washout period . | [
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PRETOX_REL | Compound - related organ weight ( absolute and covariant ) decreases were present at doses ≥ 10 mg / kg and included decreases in submaxillary salivary gland weights ( doses ≥ 10 mg / kg in males ; doses ≥ 30 mg / kg in females ) , adrenal ( doses ≥ 30 mg / kg in males and females ) , liver weights ( doses ≥ 30 mg / kg in males and 75 mg / kg in females ) and prostate weights ( males at ≥ 10 mg / kg ) . | [
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NO_PRETOX_REL | Following a 4 - week recovery period , the hematology and urinalysis parameters for animals receiving 1.2 mg / kg were comparable to vehicle control values . | [
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NO_PRETOX_REL | Merely one analysed formulation of the high dose group ( N 6437A - 9 ) exceeded with 132 % the acceptance criteria of + 15 % of the nominal concentration . | [
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PRETOX_REL | Dermal irritation consisting of very slight erythema only was noted in animals dosed twice a week . | [
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PRETOX_REL | Minimal to moderate decreases in platelet counts occurred at ~ 0.05 mg / kg in males and at ~ 0.3 mglkg in females but was resolved by the end of recovery . | [
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NO_PRETOX_REL | The area under the curve was not calculated based on two data points only and therefore any accumulation could not be assessed for this dose group . | [
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NO_PRETOX_REL | Clinical chemistry parameters showed no clear treatment - related changes in any dose groups . | [
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NO_PRETOX_REL | There were no clinical observations or toxicologically relevant effects on body weight development indicating a relationship to the treatment with COMPOUND_XXX . | [
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PRETOX_REL | Slight body weight losses were seen on day 4 in individual males at doses t 100 mg / kg / day and in individual females at all doses . | [
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NO_PRETOX_REL | XXXXXX , was administered to male rats at dosages of 60 and 180 mg / kg / day ( at a dosage volume of 5 mL / kg ) , once daily , for either 1 , 3 , 7 , 14 , 21 or at least 49 ( 180mg / kg / day only ) or 91 days ( 60 mg / kg / day only ) . | [
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PRETOX_REL | Total WBC and absolute lymphocyte counts in group 4 males remained reduced as compared to control after the 4 - week recovery period . | [
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NO_PRETOX_REL | There was no relevant effect on body weight development and food intake at 20 mg / kg . | [
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NO_PRETOX_REL | Further groups of 2 male and 2 female minipigs were treated with the placebo formulation or the 200 mg / g formulation and observed after cessation of treatment for 6 weeks to investigate the reversibility of treatment - related effects . | [
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PRETOX_REL | The decrease in the absolute organ weight of the seminal vesicles from the mid dose of 200 μg / kg COMPOUND_XXX and the additional decrease in the relative organ weight of the seminal vesicles at the high dose of 500 μg / kg COMPOUND_XXX are suspected of being compound related as the decrease is dose dependend . | [
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NO_PRETOX_REL | Ophthalmologic evaluations were conducted on all animals during pretest and on all control and high - dose animals on day 24 during week 4 . | [
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PRETOX_REL | Food consumption Food consumption was significantly reduced in animals treated with COMPOUND_XXX at a daily dose of 160 umol / kg bw . | [
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PRETOX_REL | Based on decreased organ weight in the thyroid , a no - toxic - effect level ( NTEL ) was not established . | [
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NO_PRETOX_REL | Analytical measurements from removed patches revealed that 46 - 68 % and 34 - 63 % of COMPOUND_XXX were released from the patches on days 1 and 14 , respectively . | [
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NO_PRETOX_REL | These signs abated during the recovery phase in all affected animals . | [
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NO_PRETOX_REL | Clinical signs , body weights and food consumption determination were performed on all animals during the study . | [
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NO_PRETOX_REL | Findings were as follows : Toxicokinetics : Generally greater than dose proportional increases were observed in AUC0 - 24 hr on both toxicokinetic sampling days for both genders . | [
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NO_PRETOX_REL | In conclusion , the dose level of 5 mg / kg is determined as the maximum tolerated dose ( MTD ) in dogs . | [
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NO_PRETOX_REL | After the recovery period , signs of reversibility were observed in individual animals . | [
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PRETOX_REL | Based on body weight loss and reduced food consumption in two females from the high - dose recovery group , dosing was discontinued for all group 4 animals and recovery was initiated a day earlier than originally scheduled . | [
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NO_PRETOX_REL | Blood samples for toxicokinetic analyses were collected on all animals for determination of COMPOUND_XXX plasma levels during week 2 ( day 8 ) at 0 , 2 , 4 , 6 and 18 hours following the second dose of the day . | [
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PRETOX_REL | Treatment - related clinical signs consisted of fecal changes ( females at doses ≥ 0.2 mg / kg ; males at 1.2 mg / kg ) and limited hindlimb usage / abnormal gait ( individual males at 0.2 and 1.2 mg / kg ; 3/5 females at 1.2 mg / kg ) with affected limbs often red , slightly swollen and warm to touch . | [
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PRETOX_REL | Post mortem examinations : - cholestasis ( intrahepatocellular and in the bile canaliculi ) , hydropic and fatty degeneration of hepatocytes and centrilobular necrosis in male and female animals . | [
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PRETOX_REL | Lymphocyte counts were reduced for males at 300 mg / kg / day and decreased monocyte and eosinophil counts were present at dosages of 75 mg / kg / day or above . | [
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NO_PRETOX_REL | There was no apparent difference in exposure between males and females as measured by both AUC and Cmax · There was also no increase in exposure between weeks 1 and 39 . | [
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PRETOX_REL | In addition , the male showed a moderate increase in neutrophils ( +308 % ) and the female showed a slight decrease in albumin ( - 23 % ) and total protein ( - 19 % ) . | [
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NO_PRETOX_REL | There was no mortality , ocular changes , abnormal electrocardiographic or hematological findings attributable to treatment with COMPOUND_XXX . | [
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NO_PRETOX_REL | Complete necropsies were performed and macroscopic observations were recorded . | [
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NO_PRETOX_REL | Additional control and high dose animals ( 2 / sex / group ) served as recovery animals for a 4 - week recovery period . | [
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PRETOX_REL | Treatment at 50 mg / kg / day resulted in slightly increased AST , ALT , total protein , albumin and globulin and slightly decreased A / G ratio , sodium , cholesterol and triglycerides . | [
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NO_PRETOX_REL | The purpose of this study was to investigate alterations in the thyroid in male rats administered COMPOUND_XXX at 75 mg / kg / day for 5 , 12 or 26 days ( 3 doses per week ) , compared with a positive control agent , propylthiouracil , which has known effects on the thyroid . | [
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NO_PRETOX_REL | The purpose of this study was to evaluate the potential toxicity of COMPOUND_XXX when administered to mice once daily or twice weekly by dermal skin painting for 28 days . | [
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NO_PRETOX_REL | At necropsy , gross pathology and organ weights were evaluated , and histopathologic examination of tissue specimens was conducted subsequently . | [
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PRETOX_REL | The initial high dose of 1.5 mg / kg / day caused intolerable side effects , which resulted in a dose reduction to 1.0 mg / kg / day in Week 1 . | [
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NO_PRETOX_REL | The animals were regularly monitored for viability . | [
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NO_PRETOX_REL | Comparable to the parent , the tissue concentrations of COMPOUND_XXX - D6 in the different tissues investigated were : cortex ≈ liver > pelvis at 60 mg / kg / day and liver >> cortex >> pelvis at 180 mg / kg / day . | [
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NO_PRETOX_REL | As these changes were slight to moderate in severity at 75 and 150 mg / kg / day , it is recommended that the high dosage should not exceed 150 mg / kg / day in the forthcoming 13 - week study in this species . | [
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NO_PRETOX_REL | The increase in exposure was generally dose - proportional in both male and female dogs after both a single dose and after three doses / week for more than three weeks . | [
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NO_PRETOX_REL | The cause of death could not be determined in any of these animals however , they were considered treatment - related . | [
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NO_PRETOX_REL | No signs were observed during the first 14 days oftreatment nor during the nine day extension period . | [
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PRETOX_REL | There was a local transient erythema at the application site . | [
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NO_PRETOX_REL | Ophthalmologic evaluations were conducted on all animals during pretest and on all control and high - dose animals during week 4 . | [
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PRETOX_REL | Dark livers were noted in 4/5 females and enlarged livers in 3/5 females . | [
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PRETOX_REL | No clinical signs were observed in males and females at any time point except in one male of the 75 mg / kg / day group that showed piloerection for a few days during the treatment period . | [
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NO_PRETOX_REL | Although in some instances variations from control attained levels of statistical significance , they were either of insufficient magnitude or showed no pattern to indicate an effect of treatment . | [
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NO_PRETOX_REL | Animals were dosed for 4 cycles , at doses of 0 ( control ) , 0.05 , 0.3 and 0.9 mglkg at a dose volume of 2 mL / kg . | [
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NO_PRETOX_REL | This study was designed to estimate a no - toxic - effect - level , the toxicokinetic profile , and the potential for reversal of any toxic effects within a 4 - week postdosing / recovery phase . | [
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PRETOX_REL | At 1.0 and 7.5 mg / kg / day , hunched posture was evident in both sexes , and “ Holding body close to cage floor ” , partially closed eyes and limb extension were also noted in males only at 1.0 mg / kg / day and both sexes at 7.5 mg / kg / day . | [
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PRETOX_REL | Three group 4 ( 1000 mg / kg ) males showed respiratory sounds . | [
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NO_PRETOX_REL | Histopathologic evaluation of the tissues examined in this study did not detect any toxicity . | [
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NO_PRETOX_REL | All other concentrations were within specifications . | [
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PRETOX_REL | Treatment - related very slight or well - defined erythema occasionally occurred at the application sites in groups 2 , 3 and 4 for maximally 3 days after patch removal . | [
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PRETOX_REL | An increase in the incidence of generally minimal inflammatory foci in the heart was present at 60 mg / kg , but the toxicological significance is equivocal . | [
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NO_PRETOX_REL | Enlarged livers were observed in 4/5 males and 2/5 females . | [
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PRETOX_REL | At 50 mg / kg / day , swelling ( one female ) , swollen appendages , limping , red feet , dry perineal staining and an increased incidence and frequency of swollen muzzles were noted . | [
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PRETOX_REL | At clinical pathology examination , the very few compound - related findings consisted of prolongations of Prothrombin Times in both animals at 100 mg / kg / day , related to the pharmacological activity of the compound , and variations in urinalysis parameters from 30 mg / kg / day ( increases in urine volumes and presence of proteins , reversible ) . | [
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PRETOX_REL | The mesenteric lymph nodes showed multifocal red discolorations in females . | [
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11,
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NO_PRETOX_REL | d ) Mortalities There were no mortalities during the course of the study . | [
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NO_PRETOX_REL | during the treatment period as well as during the recovery period ( p < 0.01 , Dunnett test ) . | [
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NO_PRETOX_REL | Clinical signs , body weight and food consumption determinations were performed on all the animals . | [
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NO_PRETOX_REL | Data from recovery animals was generally unremarkable . | [
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PRETOX_REL | The histopathological findings observed in the heart were paralleled by an increase in the heart weight ratio in group III ( 30/60 mg / kg ) - females . | [
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PRETOX_REL | In addition , at the mid dose of 2 mg / kg COMPOUND_XXX and higher : - decreased body weight gain in week 4 as well as over the whole treatment period ; - acinar hypertrophy in the intraorbital lacrimal gland . | [
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PRETOX_REL | In the teeth , dose - dependent degeneration and decreased iron contents in ameloblasts corresponded to discoloration of the incisors at 10 mg / kg and higher . | [
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PRETOX_REL | Piloerection was observed in all animals receiving 300 mg / kg / day . | [
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NO_PRETOX_REL | Samples of treated and Control skin were retained and the treated skin of all animals was examined microscopically . | [
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NO_PRETOX_REL | At the end of the dosing period , at 1.0 mg / kg , the mean AUC ( 0 - 24h ) was 76.7 ± 18.5 ng.h / mL and 88.4 ± 37.8 ng.h / mL for males and females respectively , Cmax , was 23.2 ± 6.63 ng / mL and 22.9 ± 8.44 ng / mL for males and females respectively and tmax , was 0.5 ± 0 h and 0.6 ± 0.3 h for males and females respectively . | [
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NO_PRETOX_REL | A concurrent control group received the vehicle control article on a comparable regimen . | [
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NO_PRETOX_REL | The purpose of this 2 - week study in rats was to aid in the selection of dosages for a proposed 13 - week study in this species . | [
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NO_PRETOX_REL | The test article was formulated as patches , each with a content of 18 mg COMPOUND_XXX , Batch Nos XXXXXX and YYYY or 0 mg , placebo Batch Nos ZZZZZ and WWWWWW . | [
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PRETOX_REL | In conclusion , dermal skin painting of COMPOUND_XXX Nail Lacquer at doses of 100 , 200 , and 270 mg / kg / day for 28 days produced test - article related findings in the treated skin sections when applied daily . | [
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NO_PRETOX_REL | Plasma levels had decreased below the limit of quantification at 24 hours in all animals , and the area under the curve could only be determined from 5 minutes to 3 hours post injection . | [
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NO_PRETOX_REL | After once weekly dosing for at least 13 weeks , exposure to COMPOUND_XXX and BJB432 was similar to the exposure after a single dose in both male and female dogs . | [
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PRETOX_REL | However , there was a reduction in overall weight gain for females given ≥ 0.6 mg / kg which appeared to correlate with slight decreases in food consumption during the treatment period . | [
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PRETOX_REL | Four males and 10 females given 400 mg / kg / day died or were euthanatized within 7 to 22 days after initiation of treatment . | [
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NO_PRETOX_REL | In the low dose group tiast was observed between 4 and 24 h post-dose . | [
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NO_PRETOX_REL | Females showed slightly higher exposure levels at doses of 30 and 100 mg / kg / day . | [
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NO_PRETOX_REL | volume of drug or vehicle administered was 10 ml ; kg / day . | [
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NO_PRETOX_REL | Out of the 18 rats / sex / group from the toxicity study , 12 rats / sex / group were sacrificed after at least 4 weeks of treatment and the remaining 6 rats / sex / group ( based on survival ) were sacrificed after at least 4 weeks of recovery . | [
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PRETOX_REL | The trachea showed a mild to moderate pyogranulomatous inflammation in single rats , in males with increased incidences of mixed subepithelial infiltrates . | [
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PRETOX_REL | Test article - related decreases in estimated food consumption were noted in both sexes at 80 mglkg / day . | [
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PRETOX_REL | In conclusion , intravenous administration of COMPOUND_XXX at doses of 0.3 , 1.0 and 3 mg / kg for 13 weeks using a once weekly dosing schedule was associated with compound - related decreases in body weight parameters , food consumption , white blood cell counts and lymphocyte counts at doses ≥ 0.3 mg / kg . | [
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NO_PRETOX_REL | Additional histopathological findings , observed with comparable incidence in both controls and treated rats ( KO ) in this study were considered to be spontaneous or incidental and none of these finding was attributed to effects of the test item . | [
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NO_PRETOX_REL | CONCLUSION Toxicokinetic results showed that following a 4 - week repeated oral administration at doses of 80 to 480 mg / kg / day of COMPOUND_XXX , all macaques were exposed to COMPOUND_XXX on dosing Days 1 and 29 . | [
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NO_PRETOX_REL | Administration of 50111 of COMPOUND_XXX at a concentration of0 .4 mg / ml was considered to be close to the maximum tolerated dose . | [
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NO_PRETOX_REL | The study was mainly focused on the histopathological , electron microscopical , and molecular biological evaluation of tissues of the heart and skeletal muscle . | [
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PRETOX_REL | Pathological examination revealed increased mastocytes ( grade 3 ) in 5/12 high dose animals and in 1/8 low dose recovery animals as swell as increased histiocytes in the mesenteric lymph nodes ( grade 3 ) in 2/19 control , 7/20 high dose , and in 2/8 high dose recovery rats . | [
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PRETOX_REL | Discussion Bone and tooth changes observed in this study were related to increased exposure to fluoride with its accumulation , and were also consistent with skeletal / dental fluorosis in rats reported in the literature ( NTP , 1990 ; Maurer et al , 1990 ; Ream , 1981 ) . | [
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NO_PRETOX_REL | The potential systemic toxicity , and reversibility of toxic effects of the test article , COMPOUND_XXX , were evaluated in this one - month study ( with a one - month recovery period ) in Crl : WI ( GLx / BRL / HAN ) IGS BR rats . | [
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"O",
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NO_PRETOX_REL | The following rounded values of Cmax and AUC ( o - 24h ) were observed on day 14 : COMPOUND_XXX Male Female COMPOUND_XXX - 666 Male Female 11 121 120 14 10 53 14 103 102 17 16 60 185 1810 1113 199 168 735 247 1637 1003 242 239 942 Cmax ( ng / ml ) 36 mg / day 108 mg / day 216 mg / day AUC o - 24h ( h.ng / ml ) 36 mg / day 108 mg / day 216 mg / day Because of the great between - animal variability , an increase of the concentration with the dose could not be demonstrated . | [
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NO_PRETOX_REL | Electrocardiography was performed at pretest , and on day 13 . | [
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] | [
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PRETOX_REL | In general , there were no differences in the severity of the findings between the two treated groups with the exception of the pancreatic lesions which were mainly observed at 10 / 100/75 mg / kg / day . | [
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PRETOX_REL | In the stomach , minimal multifocal acute hemorrhages were found in the glandular stomach . | [
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PRETOX_REL | Determination of organ weights revealed a dose - dependent increase of the relative kidney weights in 40 and 8 mg / kg / d males . | [
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2,
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3,
4,
4,
4,
4,
4,
4,
4,
5,
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] |
NO_PRETOX_REL | Blood samples were taken prior to treatment ( on the first day ) , and at approximately 2 , 6 , and 24 h following patch application on the 1st and 14th days . | [
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Subsets and Splits