Astraea

Analyze clinical study data and connect statistical protocols to trial evidence

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You can use Astraea to manage clinical study data, statistical analysis plans, and trial protocols in a single workspace. It allows clinical biometrics teams to explore patient populations, evaluate endpoints, and compare treatment arms with governed analysis. You can ask specific study questions, inspect the underlying code and data behind every generated output, and maintain complete bi-directional traceability. This helps research teams review study documents, monitor patient safety signals through profile sequences, and avoid trial errors during regulated clinical drug development workflows.

What Astraea does

Compare treatment arms across clinical endpointsConnect study protocols to statistical analysis plansInspect underlying data and code for study outputsVerify evidence traceability across clinical documentsReview patient profile sequences for safety eventsAsk questions to explore study trial datasetsInspect code and source data behind every statistical outputBi-directional traceability between protocols and study evidenceCompare treatment arms and explore endpoint populationsLink statistical analysis plans directly to study documentsTrack patient profiles and sequence clinical safety signalsAsk natural language questions about study datasets

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