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NO_PRETOX_REL | The purpose of this study was to establish the toxicologic effects of COMPOUND_XXX , a histone deacetylase inhibitor , when administered intravenously to rats for 13 weeks using a once weekly dosing schedule . | [
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PRETOX_REL | vomit and hypersalivation in males and females treated at 75 mg / kg / day , . | [
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PRETOX_REL | Sporadic food left was observed at 25 mg / kg and higher . | [
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NO_PRETOX_REL | Concerning the water intake , there were no descriptions of unusual findings in water intake in the observation records . | [
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NO_PRETOX_REL | Three groups will be treated with one formulation at three different concentrations ( 0 % , 10 % and 20 % ) . | [
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PRETOX_REL | Rales was occasionally observed in the 600 and 2000 mgikgíday groups one hour following dosing . | [
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PRETOX_REL | In animals with renal changes , the bone changes were complicated by secondary increases in bone resorption of tibia and alveolar bones . | [
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PRETOX_REL | Statistically significant drug - related decrease in body weight gains were detected in the high dose males ( 15 % ) and low ( 10 % ) , mid ( 10 % ) and high dose ( 27 % ) females . | [
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NO_PRETOX_REL | The present data set gives no indication of gender - specific differences in pharmacokinetics of COMPOUND_XXX in minipigs . | [
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PRETOX_REL | The spermatogenesis was markedly impaired . | [
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PRETOX_REL | Adrenal cortical alterations increased with treatment duration and included vacuolation , hypertrophy , single cell necrosis , hemorrhage / congestion and inflammatory cell infiltration and after the recovery period pigment deposition . | [
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PRETOX_REL | In conclusion , treatment with COMPOUND_XXX caused a notably high early mortality at a dose of 600 mg / kg / day , a dose - related decrease in serum glucose , and minimal to mild axonal degeneration in sciatic ( peripheral ) nerves of rats treated with 100 , 300 , or 600 mg / kg / day of COMPOUND_XXX . | [
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NO_PRETOX_REL | Electron microscopic evaluation of heart tissue from selected animals treated with COMPOUND_XXX at 80 mg / kg for 28 days generally showed the same ultra-morphology of all cellular organelles as the corresponding control animals . | [
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NO_PRETOX_REL | The dogs in all test article - treated groups were exposed to COMPOUND_XXX . | [
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PRETOX_REL | Electron microscopy revealed the occurrence of myeloid bodies in endothelial cells of heart and skeletal muscle which was distinct to striking and numerous after treatment with COMPOUND_XXX at 180 mg / kg / day . | [
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NO_PRETOX_REL | Various forms of Plasmodium sp , present in rare to occasional numbers , were identified microscopically in Wright 's stained blood films in animals of both sexes at doses ~ 30 mglkg / day and in two low - dose males . | [
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NO_PRETOX_REL | The exposure after approximately 11 and 25 weeks of treatment on a 3 doses / week regime was similar but was higher than exposure on Day 1 . | [
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PRETOX_REL | The principal test article - related microscopic findings consisted of thyroid changes ( ~ 0.06 mg / kg / day ) , depletion of lymphoid tissue ( ~ 0.2 mg / kg / day ) , thymic atrophy ( 0.6 mg / kg / day ) , decreased bone marrow hematopoiesis ( 0.6 mg / kg / day ) , and intracellular pigment deposition at various sites ( ~ 0.2 mg / kg / day ) . | [
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PRETOX_REL | Slight reductions in body - weight gain and food consumption were observed in males and females given 225 and 500 mgikg / day of NS and in females given 500 mg / kHday of OS . | [
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PRETOX_REL | At the high dose these lung findings escalated to diffuse foam cell aggregation associated with acute / mixed inflammation and hyperplasia of alveolar type II pneumocytes . | [
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PRETOX_REL | , 20 Due to a moribund condition animal H 062 / group | had to be sacrificed prematurely at the end of week 13 of the study ( see also , a. Clinical observations " ) . | [
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PRETOX_REL | One 30 mg / kg female showed a markedly increased GLDH value ( animal no. 36 ) . | [
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PRETOX_REL | Additionally , all group III ( 30/60 mg / kg ) - males showed a minimal infiltration with granulocytes . | [
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PRETOX_REL | As can be seen from the table , feed intake was slightly reduced in group Ill - males in comparison to control animals whereas in females no changes were observed up to and including group III . | [
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PRETOX_REL | Increased serum TSH levels and increased relative kidney weights were observed in female rats . | [
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NO_PRETOX_REL | The mechanisms of toxicity and surrogate markers were also evaluated . | [
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NO_PRETOX_REL | In uterine samples mean concentrations of COMPOUND_XXX were about 1000 times higher than the highest serum concentrations measured ( TT 1 ) . | [
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PRETOX_REL | In addition at the mid dose of 20 mg / kg COMPOUND_XXX per day and higher : Clinical examinations : - emaciation occurred in one male animal of the mid dose . | [
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NO_PRETOX_REL | Protocol - specified organs were weighed and tissues were collected , processed and microscopically examined for all animals . | [
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PRETOX_REL | The only histopathological finding related to COMPOUND_XXX treatment was minimal to slight segmental degeneration of the sciatic nerve in female rats , which was evident in at least one animal at all dose levels . | [
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NO_PRETOX_REL | Accumulations of granulocytes are absent . | [
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PRETOX_REL | Transient local effects at the application site were limited to occasional erythema , mainly at the high dose during the first 9 weeks of the study and a slightly lower body weight gain was noted in treated males of all groups including Placebo Nail Lacquer and in females at 270 mg / kg compared with sham controls . | [
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NO_PRETOX_REL | On Day I. peak plasma concentrations in males were 266 ± 340 ng / ml , 529 ± 224 ng / ml and 1007 ± 440 ng / ml for 5 , 15 and 60 mg / kg / day respectively . | [
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NO_PRETOX_REL | After treatment for 2 or 4 weeks , exposure to COMPOUND_XXX or its metabolite COMPOUND_XXX doseproportionally increased from 120 to 180 mg / kg / day while for an under - proportional increased exposure was observed from 5 to 15 mg / kg / day . | [
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PRETOX_REL | The lesion was characterized by a minimal or slight perivascular edema of larger arteries located in the proximal parts of the papillary muscle . | [
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PRETOX_REL | Adverse treatment - related effects were limited to slight , reversible degenerative changes in the sciatic nerve of female rats at all dose levels . | [
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NO_PRETOX_REL | Gravimetric organ findings The absolute and relative organ weights are listed in the appendix of the report in the form of individual values , mean values per group . | [
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NO_PRETOX_REL | There were no clinical signs of toxicity . | [
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NO_PRETOX_REL | No clinical signs were observed . | [
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NO_PRETOX_REL | The purpose of this study was to compare the toxicity and toxicokinetic profile of COMPOUND_XXX produced by a new route of chemical synthesis with that produced by the old route of synthesis . | [
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PRETOX_REL | With the exception of dermal lesions observed at the site of test article administration , no gross pathology findings were considered to be test article related . | [
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NO_PRETOX_REL | The treatment period was followed by a four - week recovery period to determine the persistence or reversibility of any treatment - related effects . | [
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PRETOX_REL | Anemia and slight increases in AST and ALT , indicative for hepatocellular damage , were further findings . | [
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NO_PRETOX_REL | No relevant body and organ weight changes were found in females . | [
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NO_PRETOX_REL | All changes were reversible on withdrawal of treatment . | [
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PRETOX_REL | Drug - related effects on food consumption were noted in Group · V animals , an approximate 10 - 15 % decrease was noted . | [
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NO_PRETOX_REL | Clinical pathology evaluations ( hematology including coagulation , clinical chemistry and urinalysis ) were conducted on all animals during pretest and week 4 and at the end of the recovery period . | [
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NO_PRETOX_REL | Complete coverage of the administration area with the test or reference item generally persisted for 1 to 5 days . | [
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NO_PRETOX_REL | Hematology and clinical chemistry were performed during the last week of the study . | [
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NO_PRETOX_REL | On Week 52 . | [
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NO_PRETOX_REL | This finding was no longer present at the end of recovery . | [
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NO_PRETOX_REL | Repeated oral administrations of 20 mg / kg / d were clinically tolerated over 7 days . | [
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NO_PRETOX_REL | COMPOUND_XXX was administered by dermal skin painting to the dorsal surface ( approximately 10 % of total body surface area ) of CD - 1 mice ( 5 / sex / group ) at dose levels of 100 , 200 or 270 mg / kg for at least 28 days . | [
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NO_PRETOX_REL | The test item , COMPOUND_XXX ( lactate salt ) Batch No . | [
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"O",
"O",
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0,
0,
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] |
NO_PRETOX_REL | There were no other effects on body weights or absolute body weight gains for males or females at doses : : : : ; 0.3 mglkg after the first dosing cycle . | [
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PRETOX_REL | Changes unrelated to COMPOUND_XXX : None Body Weights ( Tables 2 - 1 to 2 - 3 , Appendices 2 - 1 to 2 - 12 ) Changes related to COMPOUND_XXX : At 50 mg / kg , significant decreases were noted on Day 29 , and increases were noted on Days 64 to 78 , and 113 to 134 compared to the controls . | [
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NO_PRETOX_REL | The batch used for this study was XXXXXX . | [
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NO_PRETOX_REL | It is considered not to represent a potential risk to man . | [
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NO_PRETOX_REL | The concentration of the week 13 low dose formulation was outside of specification ( 116 % of target ) . | [
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NO_PRETOX_REL | The AUC 5min - 3h also increased over - proportionally in relation to the dose increase between 0.1 and 1.0 mg / kg . | [
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NO_PRETOX_REL | Conclusion / Discussion A NOAEL could not be determined under the conditions of the study . | [
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NO_PRETOX_REL | Therefore , under these study conditions , the dose of 10 mg / kg / day was considered to be a NoObserved Effect Level ( NOEL ) and the dose of 30 mg / kg / day was considered to be a NoObserved Adverse Effect Level ( NOAEL ) based on urinalysis variations and minimal microscopic findings in the diaphragm . | [
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NO_PRETOX_REL | Results Formulation analysis revealed that the dose groups were sufficiently exposed to the test item : The animals received mostly the anticipated concentrations ( 85 – 115 % ) , with the exception of 3 samples with concentrations that were slightly above the predefined acceptance limit . | [
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NO_PRETOX_REL | RESULTS General findings Tests of the reflexes showed no adverse effects up to and including group Ul { individual data see appendix of the report ) . | [
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NO_PRETOX_REL | Following oral administration , COMPOUND_XXX was quickly absorbed reaching peak plasma concentrations in approximately 0.5 to 2 hours . | [
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PRETOX_REL | A mild to moderate increase in circulating lymphocytes and neutrophils was seen . | [
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PRETOX_REL | Increases in cardiac troponin I in animals treated with COMPOUND_XXX indicated cardiotoxicity at 180 mg / kg / day and correlated with histological changes in the heart . | [
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PRETOX_REL | Organ weight changes were noted at 60 mg / kg / day , including increased heart and kidney weights in both sexes and increased liver and decreased thyroid weights in females only . | [
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NO_PRETOX_REL | Groups of 8 or 10 male control animals similarly received the above mentioned vehicle at 5 mL / kg for 3 days or 4 weeks , respectively . | [
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PRETOX_REL | Minimally higher liver weights were noted from the low dose in females with , in addition , pale liver for some females at 320 mg / kg . | [
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NO_PRETOX_REL | Organ weights No compound related findings . | [
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"related",
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] | [
"O",
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"O",
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"O"
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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 | The toxicological relevance of these findings is debatable . | [
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0,
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PRETOX_REL | Test article - related moribundity occurred during week 3 in one female at 80 mg / kg / day following approximately 9 daily doses . | [
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NO_PRETOX_REL | Selected clinical chemistry parameters were determined at the end of the study . | [
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NO_PRETOX_REL | Complete necropsies including macroscopic assessments were performed on all animals . | [
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PRETOX_REL | During the recovery period , food consumption was also reduced in animals treated with 10 umol / kg bw . | [
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PRETOX_REL | At histopathology the female rats of all dose groups ( 3 , 10 , and 30 mg / kg ) exhibited a cytoplasmatic vacuolation in the zona fasciculata of the adrenal gland . | [
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NO_PRETOX_REL | D6 is an intermediate of drug synthesis and has shown to be mutagenic in the AMES test . | [
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PRETOX_REL | Notable body weight losses occurred in individual animals as early as day 15 and persisted and / or worsened on days 22 , 26 and 29 . | [
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NO_PRETOX_REL | An additional 36 animals / sex / group received 100 , 200 or 270 mg / kg daily for toxicokinetic evaluations on Days 1 and 28 . | [
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PRETOX_REL | The increase in the liver weight ratio in males from group I ~ II are considered to be spontaneous in origin as no histopathological alterations occurred in the liver of male animals . | [
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NO_PRETOX_REL | At 25 mg / kg , significant decreases were noted on Days 50 to 64 , and increases were noted on Days 113 to 141 , 155 , 176 , and 183 compared to the controls . | [
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PRETOX_REL | T4 levels were decreased in male and female rats . | [
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PRETOX_REL | In group III , the heart rates were increased in both sexes in week 1 and 4 two hours after application respectively . | [
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NO_PRETOX_REL | A further group received 2000 mg / kg / day subdivided into 2 equal doses , separated by 1 hour . | [
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PRETOX_REL | Relative liver weight was increased in both males and females . | [
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PRETOX_REL | At post-mortem , animals given 1000 mg / kg / day had swollen hindlimbs with restricted movement of the joints . | [
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PRETOX_REL | Regarding clinical chemistry parameters , the increased GLDH observed only in one 30 mg / kg female was considered incidental . | [
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PRETOX_REL | From macroscopic and microscopic observations at premature and / or terminal kill , degenerative / atrophic changes were seen in the haemolymphopoietic system , lungs , intestines and ovaries mainly at the dose level of 40 mg / kg and were considered as toxicological targets of the compound COMPOUND_XXX as follows : - the bone marrow hypocellularity was noted in all animals given 40 mg / kg and was the histological correlate of the fluid femoral bone marrow seen for 5/10 males and 4/7 prematurely killed females given 40 mg / kg . | [
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NO_PRETOX_REL | Clinical Pathology : There were no clinical chemistry or hematology changes in rats given 40 or 160 mg / kg / day . | [
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NO_PRETOX_REL | Additionally one sample was obtained for all animals 24 hours after dosing on one occasion in Week 26 . | [
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NO_PRETOX_REL | SUMMARY AND CONCLUSIONS : Plasma samples from rats on days 1 , 15 and 29 of treatment with 0 ( vehicle control ) , 0 ( distilled water control ) , 10 , 40 , 180 or in mg / kg / day for 29 days ( protocol 05591 ) were analyzed by a solvent extraction - HPLC / UV method . | [
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PRETOX_REL | All male animals were interim sacrificed on day 10 of the test with regard to clear signs of liver toxicity detected in biochemical examinations on day 8 . | [
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PRETOX_REL | Food consumption was significantly reduced as compared to controls in males and females administered the 0.9 mg / kg dose at the end of the first , third and / or fourth dosing cycles . | [
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NO_PRETOX_REL | A control group of 3 male and 3 females received empty capsules during the treatment period and then no capsules during the recovery period . | [
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NO_PRETOX_REL | At the initiation of dosing , the animals were approximately 8 weeks of age and weighed 219.5 to 261.5 g for males and 160.6 to 196.7 g for females . | [
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NO_PRETOX_REL | Control animals received 1 % CMC only . | [
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NO_PRETOX_REL | The increase in exposure was generally doseproportional in both male and female animals . | [
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PRETOX_REL | However , the neurodegeneration induced by COMPOUND_XXX can not be regarded as a gender - specific effect since males and females were similarly affected in a 5 - day dose range - finding toxicity study [ 1 ] . | [
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