WE ARE ACCELERATING
DRUG DEVELOPMENT WITH AI-POWERED LUMIPATH™

ACCURATE. COMPLIANT. ADAPTABLE.

What took 8 weeks
now only
takes 8 minutes.

Our Mission is Clear — expedite therapies by streamlining archaic processes, reducing costs, and accelerating complex treatments to patients with Luminari’s comprehensive toolbox that includes LumiPath™ AI software.

Introduction to Luminari®™ Video - LumiPath™ application (1:50 min)

Transforming Drug Development
with Measurable Impact.

LumiPath™ doesn't just automate clinical protocol generation - it transforms it. Through specialized AI agents with deep regulatory and therapeutic expertise, we're delivering breakthrough improvements that compress development timelines, reduce costs, and accelerate patient access to life-changing therapies. The numbers tell the story of a fundamental shift in how drugs move from discovery to patients.

50%

FASTER CLINICAL TRIALS

Reduce clinical trial timelines through AI optimization

30%

COST REDUCTION

Lower development costs via streamlined processes

95%

DATA INTEGRITY

Blockchain-secured immutable trial data

2x

PATIENT RECRUITMENT

Accelerated recruitment
through AI matching

Innovative AI Solutions

Revolutionary technology stack transforming pharmaceutical development through AI and digital twin technologies.

AI Stars
LUMINARI’S AI-POWERED
DRUG DEVELOPMENT

Our proprietary AI platform streamlines clinical trial processes, eliminates errors and redundancies, and ensures the integrity of study data and outcomes.

Digital Twin people icon
'DIGITAL TWIN' VIRTUAL
PATIENT MODEL

Our virtual patient simulation tool provides real-time insights into trial dynamics, empowering sponsors to make informed decisions and optimize study design.

AI Icon
AI-DRIVEN EFFICIENCY
AND FORECASTING

By leveraging our custom-trained AI models, sponsors can quickly identify gaps, forecast desired outcomes, and make real-time adjustments - driving efficiency and ensuring trial success.

LumiPath™

an AI Regulatory
Submissions Pathfinder

Experience LumiPath
LumiPath UI screenshot
LumiPath icon

LumiPath™ eliminates the protocol development bottleneck that delays drug development and postpones patient access to critical therapies. Our multi-agent AI platform generates regulatory-compliant clinical trial protocols in minutes—complete with optimized statistical designs, comprehensive safety monitoring plans, and operational execution frameworks that reduce the 60% amendment rate plaguing today's trials.

Experience the power of AI agents trained on thousands of successful protocols across therapeutic areas, ensuring your submissions meet rigorous FDA, EMA, and ICH standards while incorporating best practices that accelerate approval timelines and trial success rates.

unravelled string graphic
Untangle the human drudgery and change lives with Luminari AI.
LUMINARI®™

AI Tools + Services

Revolutionary technology stack transforming pharmaceutical development through AI and digital twin technologies.

Lifecycle icon
Drug Lifecycle
Management
Real-time visibility across your entire development portfolio. Make informed, data-driven decisions that optimize timelines, reduce risk, and accelerate your path from discovery to market.
LumiPath Icon
LumiPath™
AI Regulatory
Submission
Pathfinder
Navigate the complex regulatory landscape with confidence. LumiPath™ generates comprehensive, submission-ready protocols that meet global regulatory standards in minutes, not months—empowering sponsors to accelerate study startup while reducing the costly amendments that delay trials and inflate development budgets.
LumiView Icon
LumiView™
Drug Trial
Executive
Dashboard
Real-time portfolio intelligence for executive decision-making. Monitor trial performance, track milestones, optimize resources, and identify risks before they impact timelines—all from a unified dashboard designed for strategic oversight.
LumiSight Icon
LumiSight™
AI Patient
Focused Trial
Insights
Accelerate enrollment and improve retention through AI-driven patient insights. Our platform identifies recruitment bottlenecks, predicts dropout risks, and provides actionable recommendations that help sponsors achieve enrollment targets faster while enhancing the patient trial experience.
Digital Twin people icon
'Digital Twin'
Virtual Patient
Tools
AI Stars Icon
AI Powered
Drug
Development
Market Access shopping cart icon
Market Access
and Drug
Commercialization
Strategy
Regulatory Submissions icon
Regulatory
and Medical
Affairs
Data services icon
Data Analysis
and Insights
Protocol Feasibility icon
Protocol
Feasibility
Sales Team presnting icon
Sales Team
Training and
Enablement
AI implementation Icon
AI
Implementation
and
Deployment
Consulting

Transform Your
Protocol
Development.

Free Trial Challenge
award badge icon

We invite you to challenge our system with your current protocol development needs. Provide the same inputs you would use in your traditional process and compare the results directly. Put Us To The Test.

Free Trial Offer Trial Overview Video (3:08 min)
Free Trial Includes:
  • Full access to Luminari's protocol development platform
  • Personalized 1:1 onboarding and support
  • Ability to process your actual research data
  • Side-by-side comparison reporting of traditional vs. Luminari-generated protocols
  • Comprehensive consultation on implementation for your specific need

What is Luminari®™

Luminari | Shaping the Future of Drug Development Innovation

By harnessing the power of artificial intelligence we are creating innovative solutions that drive unprecedented efficiency, accessibility, and patient-centricity throughout the drug development process.

Our team of industry experts and technology pioneers are dedicated to accelerating the path from discovery to delivery. We empower pharmaceutical companies, research organizations, and patients tocollaborate like never before, unlocking new possibilities in the pursuit oflife-changing therapies.

Our proprietary AI solutions are leading the transformation of the pharmaceutical industry. We envision a future where cutting-edge treatments are brought to market swiftly, with precision and affordability. Our virtual patient models predict study outcomes and optimize every step of the clinical trial journey.

Our vision is to be the catalyst for groundbreaking advancements in drug development.

Leadership Team

Powerhouse Front Bench.

Person image
Yuri Zamostin
FOUNDER AND CEO

20+ years of experience in Healthcare and life sciences.

Launched more than 35 products globally, across a variety of TA’s, including but not limited to Oncology, Neurology, Rare Disease and others.
Worked with PwC, CVS Health, BioSolutia/Caremetx, Parexel, Amgen and others.

Numerous Technology Implementation/ Digital Transformation, Operational Efficiency, and Innovative Product Development and Utilization.

Team Member
Dave Urban
Strategic Advisor

Strategic Advisor – client advocate and relationship builder

Life sciences executive with over 22 years expertise in data analytics, RWD/RWE, clinical research, market access, leadership and strategic partnerships.
Proven success driving business opportunities, managing key alliances, and exceeding sales and growth targets.

Core strengths in clinical research, commercialization, real-world data/evidence, AI, business development, strategic planning, and sales cycle and pipeline management.

Team member
Matt Liotine
CDO

Chief Data Officer – in-house geek and technology maven

Executive Advisor l Information & Decision Scientist l Operations Management
Worked on over 100 new projects with entrepreneurs and companies across the globe in numerous industries, including manufacturing, health and medical, telecommunications, information technology.

Academic rank of Professor in the Managerial Economics & Decision Sciences and Operations Management department.

Person image
Chuck Hamilton
CLO

Executive advisor and Chief Learning Officer

Executive Advisor SFU Venture Labs, startup coach, Chief Learning Officer (CLO) and former IBM Executive, Chief Operating Officer, Associate Faculty member, and TED Talker, constantly looking for ways to accelerate opportunity.

Chuck focuses on Learning Strategies, AI, Blockchain, Web3, and Digital Transformation.

Person image
John Conway
Strategic Advisor

More than 30 years of R&D leadership across the pharmaceutical and biotechnology industries.
Has previously served as Head of R&D IT/CIO for MedImmune, AstraZeneca’s biologics division, and later led Data Science and AI for AstraZeneca.

Has held senior roles at Schrödinger, Accelrys, GlaxoSmithKline, and Merck & Co. His career began with undergraduate research at Penn State, followed by roles at Tektagen (Charles River Laboratories), the Pennsylvania State Police as a forensic scientist, and STC (Orasure) as an R&D scientist. He holds degrees in biochemistry and molecular biology from Pennsylvania State University and Lehigh University.

Contact Us

Ready to Revolutionize your Clinical Trials?

Everyday clinical protocols remain in development is another day patients wait for life-changing therapies. We've built AI technology that transforms 8-week protocol generation into 8 minutes—without compromising quality.

If you're ready to accelerate development timelines, reduce costly amendments, and bring therapies to patients faster, let's talk about how LumiPath™ can transform your clinical development process!

Thank you! Your submission has been received!
Oops! Something went wrong while submitting the form.