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HPVIS Ad hoc Query

Selection of Columns

STEP 2: Select one or more column(s) for your output by clicking on the square box next to the column name. When you are finished selecting columns, click on the "STEP 3: Enter Search Criteria" button at the bottom of this page.

QUERY NAME: Skin Sensitization Data, TABLE NAME: V_MAMMALIAN_OTHER_4_EZ
	Category Chemical CAS Number	A standardized number assigned by the Chemical Abstracts Service (CAS) to identify a chemical (e.g., 10595-60-5).
	Category Chemical Name	The ninth collective index name of the category chemical.
	Challenge Exposure Period	Duration of the challenge portion of the test.
	Challenge Exposure Period Units	Time units represented by the exposure period value.
	Challenge Frequency of Treatment	Description of the administration of doses to the test animals during the challenge phase of the test (e.g., n doses per per week).
	Conclusion	Sponsor's characterization of whether the validity criteria of the test guidelines followed can be considered fulfilled.
	Consortium Name	The names of the companies that belong to the consortium or partnership if applicable.
	Control Group Type	Describe the concurrent controls used in the study
	Dose Remarks	Information about the Doses or Concentrations applied to the test subjects.
	Exposure Period	Duration of the test.
	Exposure Period Units	Time units represented by the exposure period value.
	Frequency of Treatment	Description of the administration of doses to the test animals (e.g., n doses per day, n days per week).
	Gender	Gender of the tested animals.
	GLP	Indicate if the study was conducted following Good Laboratory Practice standards. Enter Not Applicable for studies involving estimated values.
	Interpretation of Results	Overall interpretation of or conclusions drawn from the test results.
	Key Study Sponsor Indicator	An indicator entered by the sponsor specifying whether or not the Robust Summary's test results for this endpoint are summarized from a "key" or "critical" study.
	Mammalian Strain	Strain of mammal tested.
	Measurement Period	Measurement time applicable to the test result value.
	Measurement Period Units	Time units represented by the measurement period value.
	Method/Guideline Followed	The name of the Method or Guideline followed in performing the study.
	Negative Control Substance	Identify the negative control used in the test.
	Number of Organisms per Dose/Concentration	The number of organisms dosed at each dose level of the study.
	Other Species	Identify the species tested when not available from the list of standard species.
	Other Strain	The mammalian strain tested, when not available from the list of standard strains.
	Other Vehicle Name	Chemical identity of a non-standard vehicle.
	Percent Sensitized -- Negative Control	Percentage of the test subjects sensitized by exposure to this dosage of the negative control substance.
	Percent Sensitized -- Positive Control	Percentage of the test subjects sensitized by exposure to this dosage of the positive control substance.
	Percent Sensitized -- Test Substance	Percentage of the test subjects sensitized by exposure to this dosage.
	Positive Control Substance	Identify the positive control used in the test.
	Post-Exposure/Depuration Period	Observation period after last exposure to the test chemical.
	Post-Exposure/Depuration Period Units	Time units represented by the post-exposure period value.
	Program Flag	Program that the submission is associated with.
	Reliability	Indication of the adequacy of data at the discretion of the person preparing the Robust Summary.
	Reliability Remarks	Comments about how the reliability of data was determined and other related remarks. If a numeric or other coded system, such as Klimisch Codes are used to denote reliability, identify and/or define the coding system.
	Results Remarks	Sponsor provided additional descriptive text about the results of the study.
	Route of Challenge Exposure	Indicate the route of challenge exposure.
	Route of Induction	Indicate the route of induction exposure.
	Sensitization Score	Numeric characterization of the Sensitization properties of the test substance at this dosage, ranging from 0 (no Sensitization potential) to 4.
	Species or in Vitro System	Organism/cell culture used in the experiment.
	Sponsor Name	The name of the individual company or consortium (i.e., two or more companies) making a commitment in the HPV Challenge Program to provide data for a chemical or category of chemicals (e.g., Eastman Chemical Company).
	Sponsored Chemical CAS Number	A standardized number assigned by the Chemical Abstracts Service (CAS) to identify a chemical or category (e.g., 10595-60-5).
	Sponsored Chemical Name	The ninth collective index name of the sponsored chemical or category.
	Sponsored Chemical Result Type	Indicator showing whether the test result represents a measured or an estimated value for the sponsored chemical.
	Study Reference	Identify reference(s) used to compile the summary by entering: author(s), year, title, laboratory name, laboratory report number, report date (if published, list journal name, volume, pages).
	Study Type	Type of experiment performed.
	Submission Name	The sponsor provided name associated with the submission.
	Submitter's Name	The name of the individual company or consortium formally providing test plan related information.
	Test Conditions Remarks	Additional comments describing the characteristics of the Test Conditions.
	Test Substance CAS Number	A standardized number assigned by the Chemical Abstracts Service (CAS) to identify a chemical (e.g., 10595-60-5).
	Test Substance Chemical Name	The ninth collective index name of the test substance.
	Test Substance Purity	The purity of the chemical used in the study or estimation. Not applicable to mixtures. Note if not available.
	Test Type	Type of test performed.
	Total Volume Applied	The total volume of active/test substance applied/instilled.
	Total Volume Applied Units	The unit of measure applied to the total value of active/test substance.
	Unable to Measure or Estimate Justification	A short description of why neither a measured test result nor estimated value will be provided for this endpoint.
	Vehicle Amount	The amount of carrier/solvent used to deliver the test substance to the experimental system.
	Vehicle Name	Chemical identity of the vehicle
	Vehicle Units	Units of measure describing the Vehicle Amount.
	Vehicle Used	Indicator that a chemical was used to emulsify or mix the experimental chemical to enhance its solubility.
	Year Study Performed	If known, the sponsor provided year in which the test being described was conducted.

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