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Comment: TOBA-544

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Trial Elements

In this study, treatment dosing started on one date and the necropsy is scheduled, for an individual animal, after 28 to 30 days of treatmentdosing. The necropsy for a subset of animals per treatment exposure group per day will be staggered over a 3-day period.

Dataset wrap
Namete
Dataset2
RowSTUDYIDDOMAINETCDELEMENTTESTRLTEENRLTEDUR
1TDM2TESCRNScreenStart of PretreatmentPre-exposure1 week after start of ElementP7D
2TDM2TETRT01Vehicle ControlFirst day of dosing with vehicle controlDate of necropsy: 28 to 30 days after start of Element
3TDM2TETRT02100 mg/kg Drug A, once dailyFirst day of dosing with 100 mg/kg Drug ADate of necropsy: 28 to 30 days after start of Element
4TDM2TETRT03500 mg/kg Drug A, once dailyFirst day of dosing with 500 mg/kg Drug ADate of necropsy: 28 to 30 days after start of Element

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There are 3 trial arms in this study. The fact that some subjects are being selected for blood sampling is an experimental factor that is separate from the treatment being dosing being received; this is described in the TS example.

Dataset wrap
Nameta
Dataset2
RowSTUDYIDDOMAINARMCDARMTAETORDETCDELEMENTTABRANCHEPOCH
1TDM2TA1Control1SCRNScreenRandomized to Group 1PRE-TREATMENTEXPOSURE
2TDM2TA1Control2TRT01Vehicle Control
TREATMENTEXPOSURE
3TDM2TA2100 mg/kg1SCRNScreenRandomized to Group 2PRE-TREATMENTEXPOSURE
4TDM2TA2100 mg/kg2TRT02100 mg/kg Drug A
TREATMENTEXPOSURE
5TDM2TA3500 mg/kg1SCRNScreenRandomized to Group 3PRE-TREATMENTEXPOSURE
6TDM2TA3500 mg/kg2TRT03500 mg/kg Drug A
TREATMENTEXPOSURE

Trial Sets

Assuming that the protocol also specifies that subjects with blood sampling for TK analysis are experimentally distinct, the factors of interest are the treatment levels dosing levels and whether the subject is sampled for TK analysis; this leads to 6 trial sets.

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