This is an example showing example shows a sample report table, trial design, and results data of Study #123 dataset for study 123 for the determination of the in vitro genotoxicity potential of 10 tobacco products in using the in vitro Micronucleus Assaymicronucleus assay.
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title | Sample Report Table for Study 123 |
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Rows 1-2: | Show 2 records for TSPARMCD = "GLPTYP", using TSSEQ to indicate multiple records, since both GLP types apply for this example study. | Row 3: | Shows that this study was conducted as a GLP study. | Rows 4-5: | Show the study start date and study title. | Rows 6-7: | Show the version of SEND Implementation Guide and version of Controlled Terminology used in this study. | Row 8: | Shows the applicant's organization. | Row 9: | Shows that the applicant's study reference ID is not applicable. | Rows 10-13: | Show that TSGRPID has been used to link records (name, location, country) related to the test facility (TSGRPID = 1). The study director is associated with the test facility. | Rows 14-16: | Show that TSGRPID (TSGRPID=2) has been used to link the information on the testing guideline followed on this study (TSTGDNAM, TSTGDORG, TSTGDVER). | | Shows the study type for this study. | | Shows that this study includes a Mammalian Cell Micronucleus Assay. | Rows 19-20: | Show that the species is human and the cell line is TK6 lymphoblastoid in this study. |
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title | ts.xpt (trial summary, study level parameters) |
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- Assumption: Study can have more than one assay type
- Assumption: ASSAYID value of ALL means it applies to all assays in the study
| Row | STUDYID | ASSAYID | DOMAIN | TSSEQ | TSGRPID | TSPARMCD | TSPARM | TSVAL | TSVALNF |
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1 | 123 |
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ALL | TS | 1 |
| GLPTYP | Good Laboratory Practice Type | FDA |
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11 | 123 | |
| 2 | 123 | TS | 2 |
| GLPTYP | Good Laboratory Practice Type | OECD |
| 3 | 123 | TS | 1 |
| GLPFL | GLP Flag | Y |
| 4 | 123 |
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ALL | TS | 1 |
| STSTDTC | Study Start Date |
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2007123013ALLExample a Crossover study in the Rat with 3 dose levels and 3 dosing periodsthe in vitro genotoxicity potential using the in vitro Neutral Red Uptake assay |
| 6 | 123 |
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14 | 123 | ALL | TS | 1 |
| SNDIGVER | SEND Implementation Guide Version |
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Tobacco TOBACCO IMPLEMENTATION GUIDE VERSION 1.0 |
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15ALL | TS | 1 |
| SNDCTVER | SEND Controlled Terminology Version | SEND Terminology 2021- |
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032617ALLSSPONSORSponsor Organization Sponsor 18ALLSPREFIDSponsor's Study Reference ID |
| NOT APPLICABLE |
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19ALL | TS | 1 | 1 | TSTFNAM | Test Facility Name | Example |
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Tox 20ALL | TS | 1 | 1 | TSTFLOC | Test Facility Location | 10 Somewhere Street, Montgomery, AL 10000 |
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21ALL | TS | 1 | 1 | TFCNTRY | Test Facility Country | USA |
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24ALL | TS | 1 | 1 | STDIR | Study Director | Dr. R. Smith |
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25TRT | Investigational Therapy or Treatment | Drug A | 2 | TSTGDNAM | Testing Guideline Name | GUIDELINE FOR THE TESTING OF CHEMICALS No. 487 |
| 15 |
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26TRTV | Treatment Vehicle | Saline | 27TSTGDORG | Testing Guideline Organization | OECD |
| 16 | 123 | TS | 1 | 2 |
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TRTVDESC | Treatment Vehicle Structured Description | 100.46 %(w/v) ISOTONIC SODIUM CHLORIDE SOLUTION {UNII VR5Y7PDT5W} | TSTGDVER | Testing Guideline Version | 29-July-2016 |
| 17 | 123 |
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28 | 123 | ALLGLPFLGLP Flag | Y | Study Type | GENOTOXICITY IN VITRO |
| 18 |
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29MNTASTD
| GNTXAID | Genetic Toxicology Assay |
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StandardIdentifier | MNvit |
| 19 | 123 | TS | 1 |
| SPECIES | Species | HUMAN |
| 20 | 123 |
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OECD Test No. 487 | 30 | 123 | MNTASTDV | Assay Standard Version | 2016-07-29 | 31 | 123 | MNT | TS | 1 | SSTYP | Study Type | GENOTOXICITY IN VITRO | 32 | 123 | MNT | TS | 1 | SSSTYP | Study Sub Type | In Vitro Micronucleus | 33 | 123 | MNT | TS | 1 | SPECIES | Species | Homo Sapiens | 34 | 123 | MNT | TS | 1 | ?? | Test System? | TK6 Lymphoblastoid Suspension Cells | 35 | 123 | NRU | TS | 1 | ASTD | Assay Standard | NIH Publication No. 07-4519 | 36 | 123 | NRU | TS | 1 | ASTDV | Assay Standard Version | 2006-11 | 37 | 123 | NRU | TS | 1 | SSTYP | Study Type | 38 | 123 | NRU | TS | 1 | SSSTYP | Study Sub Type | In Vitro Neutral Red Uptake | 39 | 123 | NRU | TS | 1 | SPECIES | Species | Homo Sapiens | 40 | 123 | NRU | TS | 1 | ?? | Test System?? | Normal Human Keratinocyte |
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Treatment Duration will be controlled? During CT definition/revies will need to decide appropriate Treatment duration values; If not, what are best example values to show?
Row | STUDYID | ASSAYID | DOMAIN | SETCD | SET | TXSEQ | TXPARMCD | TXPARM | TXVAL |
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1 | 123 | MNT | TX | A1 | METACT | Metabolic Activation | +S9 | 2 | 123 | MNT | TX | A1 | TRTDUR | Treatment Duration | Short Term | 3 | 123 | MNT | TX | A1 | PRDCONC | Concentration of product | 0 | 4 | 123 | MNT | TX | A1 | PRDCONCU | Concentration Unit | ug/ml | 5 | 123 | MNT | TX | A1 | Product | Product Name | 6 | 123 | MNT | TX | A1 | Smoking Regime | 7 | 123 | MNT | TX | A1 | Smoke Fraction | 123 | MNT | TX | A2 | METACT | Metabolic Activation | +S9 | 123 | MNT | TX | A2 | TRTDUR | Treatment Duration | Short Term | 123 | MNT | TX | A2 | PRDCONC | Concentration of product | 1250 | 123 | MNT | TX | A2 | PRDCONCU | Concentration Unit | ug/ml | 123 | MNT | TX | A2 | Product | Product Name | 123 | MNT | TX | A2 | Smoking Regime | 123 | MNT | TX | A2 | Smoke Fraction | 8 | 123 | MNT | TX | B | METACT | Metabolic Activation | -S9 | 9 | 123 | MNT | TX | B | TRTDUR | Treatment Duration | Short Term | 10 | 123 | MNT | TX | B | TRTDUR | Treatment Duration | Long Term (or 2 parm codes, # and unit) | 11 | 123 | MNT | TX | B | PRDCONC | Concentration of product | 0 | 12 | 123 | MNT | TX | B | PRDCONCU | Concentration Unit | ug/ml | 13 | 123 | MNT | TX | B | Product | Product Name | 14 | 123 | MNT | TX | B | Smoking Regime | 15 | 123 | MNT | TX | B | Smoke Fraction | 8 | 123 | MNT | TX | C | METACT | Metabolic Activation | -S9 | 9 | 123 | MNT | TX | C | TRTDUR | Treatment Duration | Long Term | 10 | 123 | MNT | TX | C | TRTDUR | Treatment Duration | Long Term (or 2 parm codes, # and unit) | |
This example Trial Sets dataset shows information about the test conditions for set A1 and A2 in this example study. Sets A1 and A2 can be seen in the first and second rows respectively of the sample report Table 1 (above). For brevity, the TX dataset and the findings (GT) dataset do not show information for any other sets. Fully formed datasets for this example study would include information about the test conditions and findings for all sets.
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Rows 1-23: | Show trial set parameters and values that comprise the test conditions for trial set A1. Set A1 is the data for the negative control (concentration 0) with short-term exposure and metabolic activation S9. The applicant has chosen to given a long name (SET) equal to "ST+S9_C0". Set A1 is associated with the first row in the sample report table for study 123. | Rows 24-46: | Show trial set parameters and values that comprise the test conditions for trial set A2. Set A2 is the data for the short-term exposure with metabolic activation S9 at a concentration of 1250 ug/ml. The applicant has chosen to give the set a long name (SET) equal to "ST+S9_C1250". Set A2 is associated with the second row in the sample report table for study 123. |
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Dataset2 |
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Row | STUDYID | DOMAIN | SETCD | SET | TXSEQ | TXPARMCD | TXPARM | TXVAL |
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1 | 123 | TX | A1 | ST+S9_C0 | 1 | MTACTIND | Metabolic Activating Agent Name | +S9 | 2 | 123 | TX | A1 | ST+S9_C0 | 2 | METACTFL | Presence of Metabolic Activation Flag | Y | 3 | 123 | TX | A1 | ST+S9_C0 | 3 | IVTDMIN | In vitro Treatment Duration Minimum | 3 | 4 | 123 | TX | A1 | ST+S9_C0 | 4 | IVTDTRG | In vitro Treatment Duration Target | 3.5 | 5 | 123 | TX | A1 | ST+S9_C0 | 5 | IVTDMAX | In vitro Treatment Duration Maximum | 4 | 6 | 123 | TX | A1 | ST+S9_C0 | 6 | IVTDU | In vitro Treatment Duration Unit | HOURS | 7 | 123 | TX | A1 | ST+S9_C0 | 7 | RCVDMIN | Recovery Duration Minimum | 23.5 | 8 | 123 | TX | A1 | ST+S9_C0 | 8 | RCVDTRG | Recovery Duration Target | 24 | 9 | 123 | TX | A1 | ST+S9_C0 | 9 | RCVDMAX | Recovery Duration Maximum | 24.5 | 10 | 123 | TX | A1 | ST+S9_C0 | 10 | RCVDU | Recovery Duration Unit | HOURS | 11 | 123 | TX | A1 | ST+S9_C0 | 11 | INCBTMP | Incubation Temperature | 37 | 12 | 123 | TX | A1 | ST+S9_C0 | 12 | INCBTMPU | Incubation Temperature Unit | C | 13 | 123 | TX | A1 | ST+S9_C0 | 13 | ATMRHP | Atmospheric Relative Humidity Percent | 50 | 14 | 123 | TX | A1 | ST+S9_C0 | 14 | ATMCO2P | Atmospheric CO2 Percent | 5 | 15 | 123 | TX | A1 | ST+S9_C0 | 15 | SPTOBID | Applicant-defined tobacco identifier | CIG01a | 16 | 123 | TX | A1 | ST+S9_C0 | 16 | EXPTYP | | Submerged | 17 | 123 | TX | A1 | ST+S9_C0 | 17 | SAMTYP | Sample Type | Total Particulate Matter in DMSO | 18 | 123 | TX | A1 | ST+S9_CO | 18 | ITVNAM | Intervention Article Name | Tobacco ProdA | 19 | 123 | TX | A1 | ST+S9_C0 | 19 | ITVTYPE | Intervention Article Type | Negative Control | 20 | 123 | TX | A1 | ST+S9_C0 | 20 | ITVCONC | Intervention Article Concentration | 0 | 21 | 123 | TX | A1 | ST+S9_C0 | 21 | ITVCONCU | Intervention Article Concentration Unit | ug/ml | 22 | 123 | TX | A1 | ST+S9_C0 | 22 | SPDEVID | Applicant-defined device identifier | PUFFMASTER3K | 23 | 123 | TX | A1 | ST+S9_C0 | 23 | SMKRGM | Smoking Regimen | MEDIUM INTENSITY REGIMEN | 24 | 123 | TX | A2 | ST+S9_C1250 | 24 | MTACTIND | Metabolic Activating Agent Name | +S9 | 25 | 123 | TX | A2 | ST+S9_C1250 | 25 | METACTFL | Presence of Metabolic Activation Flag | Y | 26 | 123 | TX | A2 | ST+S9_C1250 | 26 | IVTDMIN | In vitro Treatment Duration Minimum | 3 | 27 | 123 | TX | A2 | ST+S9_C1250 | 27 | IVTDTRG | In vitro Treatment Duration Target | 3.5 | 28 | 123 | TX | A2 | ST+S9_C1250 | 28 | IVTDMAX | In vitro Treatment Duration Maximum | 4 | 29 | 123 | TX | A2 | ST+S9_C1250 | 29 | IVTDU | In vitro Treatment Duration Unit | HOURS | 30 | 123 | TX | A2 | ST+S9_C1250 | 30 | RCVDMIN | Recovery Duration Minimum | 23.5 | 31 | 123 | TX | A2 | ST+S9_C1250 | 31 | RCVDTRG | Recovery Duration Target | 24 | 32 | 123 | TX | A2 | ST+S9_C1250 | 32 | RCVDMAX | Recovery Duration Maximum | 24.5 | 33 | 123 | TX | A2 | ST+S9_C1250 | 33 | RCVDU | Recovery Duration Unit | HOURS | 34 | 123 | TX | A2 | ST+S9_C1250 | 34 | INCBTMP | Incubation Temperature | 37 | 35 | 123 | TX | A2 | ST+S9_C1250 | 35 | INCBTMPU | Incubation Temperature Unit | C | 36 | 123 | TX | A2 | ST+S9_C1250 | 36 | ATMRHP | Atmospheric Relative Humidity Percent | 50 | 37 | 123 | TX | A2 | ST+S9_C1250 | 37 | ATMCO2P | Atmospheric CO2 Percent | 5 | 38 | 123 | TX | A2 | ST+S9_C1250 | 38 | SPTOBID | Applicant-defined tobacco identifier | CIG01a | 39 | 123 | TX | A2 | ST+S9_C1250 | 39 | EXPTYP | | Submerged | 40 | 123 | TX | A2 | ST+S9_C1250 | 40 | SAMTYP | Sample Type | Total Particulate Matter in DMSO | 41 | 123 | TX | A2 | ST+S9_C1250 | 41 | ITVNAM | Intervention Article Name | Tobacco ProdA | 42 | 123 | TX | A2 | ST+S9_C1250 | 42 | ITVTYPE | Intervention Article Type | Product | 43 | 123 | TX | A2 | ST+S9_C1250 | 43 | ITVCONC | Intervention Article Concentration | 1250 | 44 | 123 | TX | A2 | ST+S9_C1250 | 44 | ITVCONCU | Intervention Article Concentration Unit | ug/ml | 45 | 123 | TX | A2 | ST+S9_C1250 | 45 | SPDEVID | Applicant-defined Device Identifier | PUFFMASTER2023 | 46 | 123 | TX | A2 | ST+S9_C1250 | 46 | SMKRGM | Smoking Regimen | HIGH INTENSITY REGIMEN |
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Row 1: | Shows the value of REFID=C0. This REFID refers to the trial set with a SETCD of "A1", as defined in the TX dataset. LEVEL=1 and LVLDESC="EXPERIMENTAL UNIT/TRIAL SET" indicates this identifier is referring to both the experimental unit and the unit to which the treatment is applied, and to the entire trial set. | Rows 2-5: | Show the values of 4 observational units (C0_Count1 through C0_Count4) that are within the parent experimental unit, REFID=C0. In this example assay, these observational units are also all within the same trial set, as defined in the TX dataset. | Row 6: | Shows the value of REFID=C1250. This REFID refers to the trial set with a SETCD of "A2", as defined in the TX dataset. LEVEL=1 and LVLDESC="EXPERIMENTAL UNIT/TRIAL SET" indicates this identifier is referring to both the experimental unit and the unit to which the treatment is applied, and to the entire trial set. | Rows 7-10: | Show the values of 4 observational units (C1250_Count1 through C1250_Count4) that are within the parent experimental unit, REFID=C1250. In this example assay, these observational units are also all within the same trial set, as defined in the TX dataset. |
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Dataset2 |
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| Row | STUDYID | SETCD | REFID | PARENT | LEVEL | LVLDESC |
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1 | 123 | | C0 |
| 1 | EXPERIMENTAL UNIT/TRIAL SET | 2 | 123 | A1 | C0-Count1 | C0 | 2 | OBSERVATIONAL UNIT | 3 | 123 | A1 | C0-Count2 | C0 | 2 | OBSERVATIONAL UNIT | 4 | 123 | A1 | C0-Count3 | C0 | 2 | OBSERVATIONAL UNIT | 5 | 123 | A1 | C0-Count4 | C0 | 2 | OBSERVATIONAL UNIT | 6 | 123 | A2 | C1250 |
| 1 | EXPERIMENTAL UNIT/TRIAL SET | 7 | 123 | A2 | C1250-Count1 | C1250 | 2 | OBSERVATIONAL UNIT | 8 | 123 | A2 | C1250-Count2 | C1250 | 2 | OBSERVATIONAL UNIT | 9 | 123 | A2 | C1250-Count3 | C1250 | 2 | OBSERVATIONAL UNIT | 10 | 123 | A2 | C1250-Count4 | C1250 | 2 | OBSERVATIONAL UNIT |
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Rows 1-3, 8: | Show percentage result values that apply to GTREFID=C0. REFID=C0, as shown in the RELREF dataset, relates this data to the trial set in the first row of table 1 in the sample report table for study 123. | Rows 4-7: | Show the 4 micronucleated cell counts for the observational units with GTREFID from C0-Count1 through C0-Count4, for which their relationship to test conditions (in tx.xpt) and experimental units (in relref.xpt) are shown in the RELREF dataset. | Rows 9-11, 16: | Show percentage result values that apply to GTREFID=C1250. REFID=C1250, as shown in the RELREF dataset, relates this data to the trial set in the second row of table 1 in the sample report table for study 123. | Rows 12-15: | Show the 4 micronucleated cell counts for the observational units with GTREFID from C1250-Count1 through C1250-Count4, for which their relationship to test conditions (in tx.xpt) and experimental units (in relref.xpt) are shown in the RELREF dataset. |
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Dataset2 |
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Row | STUDYID | DOMAIN | GTSEQ | GTREFID | GTTESTCD | GTTEST | GTCELLEV | GTORRES | GTORRESU | GTCOLSRT | GTSTRESC | GTSTRESN | GTSTRESU | GTDTC |
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1 | 123 | GT | 1 | C0 | | Relative Increase in Cell Count | 154 | 0 | % |
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11 | 123 | MNT | TX | C | PRDCONC | Concentration of product | 0 | 12 | 123 | MNT | TX | C | PRDCONCU | Concentration Unit | ug/ml | 13 | 123 | MNT | TX | C | Product | Product Name | 14 | 123 | MNT | TX | C | Smoking Regime | 15 | 123 | MNT | TX | C | Smoke Fraction | Expand |
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title | gt.xpt (similar to LB) |
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BLEO & CPA - positive controls? |
Row | STUDYID | ASSAYID | DOMAIN | TXCD | GTSEQ | GTTESTCD | GTTEST | GTCELLEV (cells evaluated) | GTORRES | GTORRESU | GTSTRESC | GTSTRESN | GTSTRESU | GTDTC | GTNOMDY | GTELTM | GTTPTREF |
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1 | 123 | MNT | GT | A2 | 1 | RICC | 134 | 15.7 | % | 15.7 | 15.7MNTA2213.134 | 13.13.MNTA23C0 | RPD | Relative Population Doubling |
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1347.97.9 | 7.9MNTA24MNCELLS326620Cells | 20 | 20 | CellsMNT | A25MNCELLS219017Cells | 17 | 17 | CellsMNT | A26MNCELLSMNCE | Micronucleated Cells | 2758 |
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13Cells | 13 | 13 | CellsMNT | A27MNCELLS271421Cells | 21 | 21 | CellsMNT | A28AVGREL | Average Relative MN FrequencyMNCECE | Micronucleated Cells/Total Cells |
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666666MNT | A11154 | Relative Increase in Cell Count | 134 | 15.7 |
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00 | 0MNTA12C1250 | RCC | Relative Cell Count |
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154134 | 13.0 | % |
| 13.0 | 13.0 | % | 2022-05-25 | 11 | 123 |
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MNTA13154 | Relative Population Doubling | 134 | 7.9 |
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00 | 0MNTA14MNCELLSMNCE | Micronucleated Cells | 3266 |
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15Cells | 15 | 15 | CellsMNT | A15MNCELLSMNCE | Micronucleated Cells | 2190 |
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13Cells | 13 | 13 | CellsMNT | A16MNCELLSMNCE | Micronucleated Cells | 2758 |
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17Cells1717 | Cells | MNTA17MNCELLSMNCE | Micronucleated Cells | 2714 |
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12Cells | 12 | 12 | CellsMNTA18AVGREL | MNCECE | Micronucleated Cells/Total Cells |
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Average Relative MN Frequency575757
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Product, Smoking Regime (e.g. Traditional combustible, ENDS), Smoke Fraction, etc. https://www.itis.gov/servlet/SingleRpt/SingleRpt?search_topic=TSN&search_value=969610#null One study (Original sample of TK6 cells); (6 rows in GT) Assay (MNT) (ran on 10 tobacco products) 3 assay/test conditions; Treatment duration (2: ST, LT); Presence of metabolic activation (2: presence, type) Concentrations of product (6 of these: 0, x, y, z,..., +CNTL); CytoTox % (3 different percentages from testing 1 portion of the original sample) 4 MN counts conducted (on 4 different portions of original sample?) EID (5 of these, Count1 - Count4 and Cytotox): with many TX Parm codes?? Cytotox: RICC, RIC, RPD, #cells?? (also see Gentox notes on how to approach modeling, to apply that here?) |
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title | te.xpt (trial elements) |
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(Do we need this? a single element (treatment)?)
Row | STUDYID | ASSAYID | DOMAIN | ETCD | ELEMENT |
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(Do we need this? one arm for each trial set?)
Row | STUDYID | ASSAYID | DOMAIN | ARMCD | ARM | TAETORD | ETCD | ELEMENT |
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| Row | STUDYID | DOMAIN | ENID (Entity ID) | RICC | RCC | RPD | Sum of cell ev. | Cells with MN | SMKFID (Smoke Fraction) | REPLCTID (Replicate Number) | PLATEID (Plate ID) | COLID (Column number) | ROWID (Row number) | SETCD (Set Code, TX) | RFSTDTC | RFENDTC | RFXSTDTC | RFXENDTC | RFCSTDTC | RFCENDTC | ARMCD
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