Unlocking Billions in Lost Drug Development Investment

One Trial at a Time

An operating system for Clinical Trial Design and Execution

An 'Analog' Process Needing a Digital Intelligence Upgrade

Clinical trials are plagued by inefficiencies that cost billions and delay life-saving treatments

01 Slow

Manual iteration and resource-intensive workload. Critical data buried in massive information volumes.

02 Costly

Average cost to get a drug to market: $2.6B. Delays cost millions (Avg $40K/day in Phase 3).

03 Opaque

Black-box decision making without audit trails. Volume of information means research isn't exhaustive.

04 Risky

Bias leading to regulatory and commercial failures. Design complexity causes failures and delays.

05 Siloed

Complex workflows that don't engage ALL stakeholders lead to designs that can't be executed.

Purpose Built to Integrate Workflow & Process Understanding

An operating system for trial cognition - bringing tech leadership and agentic intelligence to the clinical trial industry

Integrated End-to-End Platform

Unifying clinical development and clinical operations in one comprehensive system that streamlines complex collaboration.

Streamlined Communication & Workflows

Breaking down silos between stakeholders with intelligent workflow automation and real-time collaboration tools.

Strategic Planning & Intelligent Design

Catalyzing coordinated execution through AI-powered insights and perspective-aware decision making.

Empowering All Stakeholders

Maximizing trial success by ensuring every voice is heard and every perspective is considered in the design process.

The Strategic Play: Build Where Others Can't Compete

🏆 WHERE WINNERS BUILD
Application Layer
AdjuvantIQ

Domain expertise + Regulatory knowledge = Unbeatable moat

THE COMPETITIVE MOAT
📦 COMMODITIZING FAST
Infrastructure Layer

ChatGPT • Claude • LangChain • AutoGPT

💡 The Insight

While everyone fights over generic AI infrastructure, biotech sponsors win by owning purpose-built applications that competitors can't replicate

24/7 Expert Agents Providing Limitless Impact

Multi-agent collaboration with built-in governance and perspective-aware reasoning

MoA Tagger

Mechanism of Action analysis and classification for drug compounds with intelligent tagging.

Compliance Sentinel

Regulatory alignment with GCP (Good Clinical Practice) validation and real-time compliance monitoring.

Biostat Sidekick

Statistical design with REML (Restricted Maximum Likelihood) and Bayesian optimization plugins.

Design Critic

Multi-perspective protocol evaluation across all stakeholder viewpoints with bias detection.

Writer Assistant

Context-rich documentation generation for protocols and regulatory submissions.

TrialSight Engine

Real-time analytics and contextual insights for optimized trial design and execution.

🛡️ OGSP Governance Framework

Ontological Governance-Schema Protocol provides zero-trust credentialed access and complete audit trails for all agent interactions

Experienced Founders with an Outside Perspective

A proven leadership combination of strategic execution and technical innovation

DH

Doug Henston

CEO & Co-Founder

Serial company builder with 25+ years scaling frontier innovations from lab to market. Yale biophysics, Harvard MBA, Naval Aviator, and Goldman Sachs veteran who raised $400M+ for regulated ventures. Disciplined risk management and institutional funding expertise.

NH

Ned Harvey

Head of Product & Co-Founder

Engineering innovator and Harvard MBA with 20+ years pioneering data-driven solutions. Former Naval Submariner, Digital Gaia co-founder, and RMI Climate Intelligence architect. Specializes in translating complex systems into market-ready products.

Join the Founding Cohort of Agentic Biotech Leaders

Be among the first sponsor companies to transform protocol development from months to hours

🚀 Launch

Design Archetype Discovery pilot with your next protocol

🔧 Onboard

Gain access to Copilot, MoA-Tagger, and Biostat Sidekick modules

✅ Validate

Participate in OGSP credentialing and provide feedback on workflows

📝 Co-Author

Collaborate on validation paper aligned to Forrester AI guidance

🎯 Shape Future

Influence AdjuvantIQ roadmap and feature priorities as founding partner

We'll respond within 24 hours to discuss your pilot opportunity

Limited Time Pilot Program

We're accepting only 25 founding partners for our initial pilot program. Join the companies already transforming their clinical development process.

$75-120M

Projected Year 5 ARR

~6,400

Target SME Market

15-20x

LTV/CAC Ratio