Solutions / R&D and Clinical
Trial MetricsClinical trial design and feasibility, benchmarked to your peers
Side-by-side trial details and customizable peer aggregates so you can ground endpoints, inclusion and exclusion criteria, enrollment targets, timelines, and feasibility in what comparable trials actually did.
- 610,000+ trials
- Refreshed daily
- Source-traceable
- Deep China coverage
Design trials with peer benchmarks
Build a peer set from 610,000+ source-traceable trials, then benchmark the choices that shape a protocol, from endpoints to enrollment, so your design decisions rest on precedent rather than assumptions.
Explore clinical trial details
View each trial's study outline as provided by global registries for side-by-side comparison across indication, endpoints, inclusion and exclusion criteria, enrollment, site locations, investigators, contact information, and more.
Build a custom peer set
Assemble the exact set of comparable trials by indication, phase, modality, geography, specific sponsors, and more, then benchmark against it.
Benchmark design choices
Establish aggregate study duration, target vs actual enrollment, site counts, and more to set benchmarks and identify what is standard vs. what is differentiated.
Pressure-test feasibility
Assess whether a design is feasible before you commit, using real precedent across sites, geographies, and timelines.
An example benchmark, ready in minutes
Choose a peer set and TrialForge aggregates the design and operational benchmarks that matter, every figure traceable back to its registry record.
Illustrative example, gene therapy in Duchenne muscular dystrophy (18 trials)
22
Median sites
36 mo
Median duration
9
Countries
Enrollment, target vs actual (median)
Site distribution