An AI-powered, in-context assistant embedded directly into the elluminate® Clinical Data Intelligence Platform
Interrogate your data as questions arise
Four synthetic adverse events are flagged as causing treatment discontinuation: allergic cough, death, intractable pain, and pregnancy. Each affects one subject; grades range from 1–5, and all four are recorded as serious adverse events.
Understand findings in study context
The strongest synthetic signals are an early three-subject cluster within 3–6 weeks, 13 related or possibly related events in the first 30 days, and later cardiac and hematologic events consistent with cumulative toxicity.
Dig deeper into discrepancies, patterns, and subjects
Eighteen synthetic adverse-event records are Grade 3 or higher but not serious, while one event is serious at Grade 1. Most high-grade, non-serious discrepancies occur at sites 0001–0003.
Address findings without leaving your workflow
A simulated issue draft is prepared for the 18 synthetic adverse-event records with a potential mismatch between toxicity grade and seriousness. Reviewers are asked to confirm whether each seriousness flag or grade is correct and update the record as appropriate.
Early adopters have seen:
