The Story
Clinical trials often fail for operational reasons introduced before the first patient is enrolled.
Feasibility and site-selection, decisions driven by fragmented data and intuition, introduce much of the downstream risk.
Hyvv exists to bring clearer signal quality and accountability to early trial planning.
The Vision
We envision a future where clinical trials are planned with materially greater predictability using trusted, explainable intelligence instead of static assumptions.
Better decisions upstream mean faster timelines, less waste, and greater patient impact.
The Platform
Hyvv is building a layered Clinical Trial Intelligence Platform for regulated, enterprise environments, designed to integrate with existing systems, not replace them.
Hyvv's Clinical Trial Intelligence Platform
The Data That Powers Hyvv
Hyvv connects and harmonises multiple complementary data layers - clinical, demographic, behavioural, and institutional - to generate trial-specific, site-level intelligence.
Individually, these datasets offer partial insight. Combined, they enable explainable predictions grounded in how trials actually operate in practice.
Clinical Trial Intelligence Platform
Predictive, explainable feasibility and site-selection intelligence.
Predictive Feasibility Engine
Trial-specific signals to identify site risk, readiness, and enrolment potential.
Explainable Decision Intelligence
Clear rationale behind every recommendation designed for regulated teams.
A connected suite of intelligence products designed to improve decision quality across the research lifecycle, starting with feasibility and site selection, where risk, cost, and delay are introduced.
Why It Matters
Accurate
Surface real-time, verifiable data signals to guide defensible decision-making.
Trusted
Preserve institutional knowledge across teams and trials to build lasting confidence.
Fast
Accelerate feasibility and reduce decision cycles from weeks to days.
Who We Work With
Hyvv is designed to support the entire research and clinical trial ecosystem, aligning sponsors, CROs, sites, investigators, institutions, and funders around accurate, trusted intelligence.
Pharma
Strengthen site feasibility with verifiable data and reduce R&D risk.
CROs
Build sponsor trust through transparent, data-driven recommendations.
Principal Investigators
Highlight performance, recruitment, and expertise to attract future trials.
Biotech
Accelerate trial readiness with faster, evidence-based site selection.
Academic Trial Units & Sites
Preserve institutional knowledge and showcase proven site capabilities.
Funding Bodies
Gain visibility into outcomes and impact with transparent, data-backed reporting.
Build the Next Generation of Research Intelligence
We’re collaborating with leading partners across pharma, biotech, CROs, and research institutions to co-develop the platform. Reach out to find out more.