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Analytics

Cortellis APIs are back online

Dear Life Sciences Data Products users,

As of 2:30pm EDT, Wed, June 19th, the Cortellis APIs are back online! Our sincere apologies for the inconvenience!

The Analytics API combines selected data from the Investigational Drugs, Clinical and Patents APIs in a format suitable to enable graphical analysis in tools like Microsoft Excel, TIBCO Spotfire, Tableau Software or QlikView.

It enables extraction of data on trials, drug pipelines, patents and adverse events using 10 pre-defined functions. Additional details can be obtained for trials using the 2 references calls.

Analytics API can help you to

  • Import information into specific analysis tools, allowing precise manipulation of the data to display exactly what is required
  • Build visual dashboards, instantly displaying at a glance a candidate’s progression through trials
  • Compare aggregated trial adverse events between drugs to evaluate their safety profile

Content

  • Development history data for drug candidates, specifically each combination of development phase, country, indication and organization
    • Ci view – Action | AuthorityGroup | Company | Country | Drug | EntityType | HighestDevStatus | HighestDevStatusForInd | Indication | IsActiveCompany | LatestChange | ParentCompany | Status | StatusDate | StatusSortCode | TherapyArea
  • Patent applications, specifically each combination of patent status, country, indication and organization
    • Patents view – Action | AuthorityGroup | Company | CompanyOwnershipRelationship | Country | Drug | DrugRelationship | EntityType | HighestPatStatus | HighestPatStatusForCnty | HighestPatStatusIdForCnty | Indication | LatestChange | ParentCompany | Patent | Status | StatusDate | StatusSortCode | TherapyArea
  • Trial information as data points or as summaries limited to trials with outcomes
    • Trial program view – Ancestry | ArmCount | DevStatus | Drug | Endpoint | EndpointReached | HasHealthyVolunteers | HighestDevStatusForInd | Indication | ProtocolAcronym | ProtocolTitle | Sponsor | StudyType | Trial id | TrialStartDate | TrialStatus
    • Trial program refs view – AdverseSummary | Description | DevStatus | Indications | OutcomeSummary | ProtocolTitle | References | TreatmentSummary | Trial id | TrialStatus
    • Trial duration refs view – ArmCount | Biomarkers | Condition | Controls | DevStatus | Drug | EnrollmentCount | Interventions | # of Patients | ProtocolAcronym | ProtocolTitle | Reference | Sponsor | Trial id | TrialStartDate | TrialStatus
    • Trial duration view – DevStatus | Drug | Endpoint | Indication | OriginatorSponsored | # of Patients | ProtocolTitle | Trial id | TrialEndDateActual | TrialEndDateCalc | TrialEndDateEstimate | TrialEndDateGiven | TrialStartDate | TrialStatus
  • Trial adverse events information as data points or as summaries limited to trials with outcomes
    • Trial safety view – AdverseEvent | AdverseIndicationCode | DevelopmentStatus | Dose | Drug | Intervention | MeddraAdverseEvent | Patients | PercentAffected | ProtocolDose | Trial id | Units
    • Trial safety refs view – AdverseSummary | Description | DevStatus | Drugs | Indications | OutcomeSummary | ProtocolTitle | References | TreatmentSummary | Trial id | TrialStatus
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