Company profile

Phesi

Clinical Trials & Research

Company profile

About Phesi

Phesi is a global provider of patient-centric data science solutions for clinical development, serving pharmaceutical and life sciences companies. The company's award-winning Trial Accelerator™ platform is powered by the world's largest clinical trials database, containing real-world data from over 325 million patients across 232 countries and territories, drawn from 719,183 clinical research projects and 22 global registries. Phesi's AI-driven solutions enable sponsors to optimize protocol design, create Digital Patient Profiles and Digital Twins, select high-performing investigator sites and countries, and generate Digital Trial Arms as external controls. By connecting real-world patient data with trial execution data, Phesi helps life sciences companies eliminate costly trial failures and protocol amendments, improve patient population accuracy and diversity, reduce trial timelines and patient burden across every stage of clinical development for any indication, including rare diseases. The company's proprietary integrated methodology and AI technologies analyze over 485,000 curated clinical trials, 4.2 million physicians, and 4,000+ disease indications. Phesi's approach transforms clinical development into a data-driven science, enabling predictive modeling across four key views: Patient Profile, Trial Performance, Country, and Investigator Site. The platform generates reliable evidence for drug development and commercialization without the expense or time required in traditional trials, helping pharmaceutical companies make more informed decisions and accelerate the path from research to market.

Company description Phesi official website

Primary marketClinical Trials & Research
Commercial modelCommercial information available on request
Company presenceOfficial website
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01 · Operating footprint

Where the Company operates

Company-profile context for clinical focus, customers, deployment, integration, milestones, and partnerships.

Clinical focus

  • 4000+ disease indications
  • Breast cancer
  • C. difficile infection
  • Iron overload
  • NSCLC
  • Oncology
  • Rare diseases
  • Type 2 Diabetes Mellitus

Who it serves

  • Biotechnology companies
  • Life sciences companies
  • Pharmaceutical companies

Deployment & integration

Cloud Saas deployment with recorded integration context.

Geographic context

MarketsGlobal - 232 countries and territories
Company sourceOfficial website

Company milestones

Platform expansion

Won 2025 Clinical Trials Arena Excellence Award for Innovation (November 2025). Took leading position on Frost and Sullivan's Frost Radar™ for AI-enabled clinical trials (February 2026). Published major analysis of 600,000+ clinical trial protocols (May 2026).

Partnerships

Recorded partners

  • Sanofi
  • Takeda

02 · Flagship portfolio

Products, workflows, and platform capabilities

Selected source-backed Company products and the available commercial context.

Countries and Investigator Site Selection

Select lead enrolling countries and investigator sites using AI-powered data analytics

Service · Cloud SaaSCompany source

DE&I Data Service

Improve diversity, equity, and inclusion in clinical trial design and patient recruitment

Service · Cloud SaaSCompany source

Digital Twins & Digital Trial Arms

Model diseases and patient outcomes using digital patient profiles and real-world data

Service · Cloud SaaSCompany source

Protocol Design and Optimization

Eliminate costly trial failures and protocol amendments using modal design value simulation

Service · Cloud SaaSCompany source

Strategic Development Planning

Plan clinical development programs using comprehensive data analytics and AI insights

Service · Cloud SaaSCompany source

Trial Accelerator

AI-powered platform for patient-centric clinical trial design and execution using real-world data

Platform · Cloud SaaSCompany source

Trial Health Check & Rescue

Monitor and rescue underperforming clinical trials using real-time data analytics

Service · Cloud SaaSCompany source

03 · Research intelligence

Research Intelligence evidence

Publications, preprints, clinical validation, and regulatory records in Evidence Position order.

Evidence position

Publications, clinical validation, and regulatory records connected to this Company appear here.

Research

Publications & preprints

Construction of a digital twin of chronic graft vs. host disease patients with standard of care.

Bone marrow transplantation · Sep 1, 2024

Clinical validation

Clinical-trial records

No linked records are currently available.

Regulatory

Regulatory records

No linked records are currently available.

04 · Company-reported outcomes

Outcomes and case studies

Company-reported outcomes and customer stories are distinct from linked Research Intelligence evidence.

Trial timeline reduction

Significantly quicker and cheaper development time through adaptive trial design optimization

Protocol amendment reduction

Eliminate costly trial failures and protocol amendments using modal design value simulation

Patient recruitment improvement

Improve patient population accuracy and diversity

Undisclosed Pharma - C. difficile infection

Protocol design optimization and investigator site selection for C. difficile infection trial

Undisclosed Pharma - Iron Overload

Protocol optimization and study feasibility for Iron Overload Integrated Development Plan, Phase 1B Trial

Undisclosed Pharma - NSCLC

Protocol design, country and investigator site selection for Non-Small Cell Lung Cancer trial

Undisclosed Pharma - Type 2 Diabetes

Protocol design and investigator site selection for Type 2 Diabetes Mellitus (T2DM) trial

Sanofi

Using Phesi's systematic analysis of clinical trial, protocol, and site space to inform new clinical programs and save existing ones

Phesi described as 'on the frontiers of defining clinical development as a science' by former SVP, Global Chief Medical Officer

Takeda

Adaptive trial design optimization for priority asset development

Significantly quicker and cheaper development time achieved through optimized adaptive trial design

05 · Leadership

Leadership team

Leadership profiles and professional links from the current Company record.

Dr. Gen Li

Dr. Gen Li

Founder, President and CEO

LinkedIn

06 · Company updates

Updates from Phesi

Recent articles published on Phesi's official website.

No Company updates are currently listed.

07 · HAIC coverage

Coverage and analysis

Health AI Central reporting that mentions this Company.

No HAIC coverage is currently linked to this Company.

08 · Official presence

Company sources and channels

Curated official destinations from the active Company record.

09 · Market pathway

Additional Companies in this Market

Other active Companies in the same market, selected alphabetically from the HAIC directory.

Market context

Clinical Trials & Research

Companies using AI to optimize clinical trial design, accelerate patient recruitment, match patients to trials, predict trial outcomes, or improve clinical research efficiency. Includes patient enrollment and screening platforms, AI-powered trial matching, and tools that reduce the time and cost of bringing new treatments to market.

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10 · Pro research

Coming soon

Expanded Company research is in development.

Health AI Central Pro · Coming Soon

Deeper Company research is coming soon.

Pro Research will introduce expanded technical context, linked evidence analysis, and comparative Company research.

ResearchEvidence analysis

Linked research, clinical, and regulatory source pathways.

CompanyTechnical context

Expanded product, deployment, integration, and partnership research.

MethodSource & review record

Record-level provenance and review context.

Coming Soon