Understand every study before the first patient is enrolled.
Trial Intelligence reads your study, structures its design, and surfaces the operational, data, and execution risks that matter before enrollment begins.
It produces two deliverables: a free Executive Summary from a public ClinicalTrials.gov NCT, and a paid Study Intelligence Report from that same NCT or from your full protocol. Same engine, same rendered provenance, same versioned generation record.
Free from a public ClinicalTrials.gov NCT. Full-protocol analysis available through a 1-hour paid strategy session under NDA.
Executive Summary · Sample
Phase III Immunotherapy Plus Chemotherapy Study in Advanced Non-Small-Cell Lung Cancer
NCT02****** · Global Oncology Sponsor
Phase
3
Enrollment
616
PTII™ v1
84/100
High Complexity
Protocol Complexity (PCI)
87
Operational Burden (OBI)
82
Eligibility Strictness (ESI)
71
Amendment Risk (ARI)
V2
Enrollment Velocity (EVI)
V2
Executive Bottom Line
Operational burden is driven by combination dosing logistics and tumor-tissue requirements during screening. Eligibility narrows the pool to recently diagnosed patients without prior systemic therapy.
Included in the Study Intelligence Report
Site network expansion recommended
Screening pool narrows sharply at community oncology sites; academic and tertiary sites recommended.
Reproducibility ID and independently versioned engine recordTier 2
Tier 2 · Paid
Study Intelligence Report
The complete analysis a clinical-development team can review and defend. Comprehensive, source-backed, and reproducible.
Input: NCT or full protocol
Everything in the Executive Summary
Full protocol analysis and source-cited risk breakdown
Operational burden and site complexity analysis
Visit schedule and endpoint analysis
CRF and SDTM domain recommendations
Statistical, monitoring, and submission-readiness considerations
PTII composite and contributing sub-indices
Every finding traceable to protocol section, engine version, evidence record, and source hash
Independently versioned engine and assessment record
Reproducibility ID for controlled re-generation
When you are ready to build, the Protocol Design Workspace (Tier 3) generates eCRFs, SDTM mapping, and the Schedule of Assessments from your protocol synopsis. The full PrismCDM Platform (Tier 4) runs the study to submission.
AI without provenance is difficult to trust. Clinical teams need to understand not only what AI recommends, but how it reached every conclusion.
The PrismCDM thesis
Early Access
Start with one study.
Generate a free Executive Summary from a ClinicalTrials.gov NCT in minutes. When you are ready, we walk through the full Study Intelligence Report on your protocol, every finding tied to its source, and show how the same platform continues through Protocol Design Workspace and the full PrismCDM Platform.