Attribute | Schema Datatype or Enumeration | Usage | Definition | Business Rules |
---|---|---|---|---|
OID | oid | Required | Unique identifier for the StudyEndPoint element | The OID attribute for the StudyEndPoint must be unique within the study. |
Name | name | Required | Human readable identifier for the StudyEndPoint element. | The Name must be unique within the set of StudyEndPoints elements for the study. |
Type | (Simple | Humane | Surrogate | Composite) | Optional | The type of end point | Simple: measures the change of a single outcome that is meaningful in the context of the disease being studied.
ODM-52
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STATUS
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Level | (Primary | Secondary | Exploratory) | Optional | Level for the Study Endpoint | These are defined in concordance with the ICH M11 Clinical electronic Structured Harmonised Protocol Specification Primary endpoint(s) are typically efficacy measures that address the main research question [1] Secondary endpoints are generally not sufficient to influence decision-making alone, but may support the claim of efficacy by demonstrating additional effects or by supporting a causal mechanism. [2] Exploratory endpoints (where nominated), they typically capture outcomes that occur less frequently or which may be useful for exploring novel hypotheses. [1] [1] US Department of Health and Human Services F . 2017. Center for Drug Evaluation and Research (CDER) and Center for Biologics Evaluation and Research (CBER): Multiple Endpoints for Clinical Trials: Guidance for Industry. (https://www.fda.gov/regulatory-information/search-fda-guidance-documents/multiple-endpoints-clinical-trials-guidance-industry) [2] Biomarkers EndpointS and other tools (BEST) http://www.ncbi.nlm.nih.gov/books/NKB338448/ |
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