Real-time Clinical IntelligenceClinical Intelligence
Predict Drug Approvals
Before the Market
Evidence-based probability scores synthesized from ClinicalTrials.gov, FDA adverse events, and SEC regulatory filings. Know the odds before anyone else.
Popular Queries
3
Data Sources
24h
Update Cycle
FDA
FAERS Data
SEC
NLP Analysis
How It Works
Our engine aggregates three independent data streams to compute probabilistic FDA approval scores.
Clinical Trials
Real-time ingestion from ClinicalTrials.gov. Track phase transitions, enrollment, endpoints, and status changes for any drug candidate.
Phase 1: 8% → Phase 3: 65% baseline
Safety Signals
OpenFDA FAERS adverse event analysis. Compare drug safety profiles against mechanism class baselines to detect elevated risks.
GLP-1 class baseline comparison
Regulatory Sentiment
NLP analysis of SEC 10-K, 10-Q, 8-K filings. Extract FDA meeting outcomes, risk factor changes, and regulatory language shifts.
Sentiment quartile scoring