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New Medicine: Faster, Safer, Smarter.

Currently, efficiency issues in Clinical Trials are costing between $600,000 - $8m dollars per day, and are significantly delaying the delivery of new medicine to patients in need.
We want to change that.

ClinTex are a solution provider to the pharmaceutical industry, and the team behind CTi – Clinical Trials Intelligence: a new type of software platform aimed at transforming the medicine development industry through the application of predictive analytics, machine learning, and the novel use of blockchain technology and smart contracts in clinical trials.

Our mission is to bring down the cost of medicine and improve the speed to market of new medicines for the people who need them, through vastly reducing development costs for the global pharmaceutical industry.

Clinical Trials Intelligence

Clinical Trials Intelligence is a distributed technology platform that incorporates predictive data analytics, machine learning (AI), and the innovative use of smart contracts to drive significant quality and operational improvements in clinical trials.

  • With the application of powerful and insightful data analytics functionality across administrative, operational and clinical functions, stakeholders can now identify, action and resolve the potential issues detected before they  negatively impact the trial.
  • Advanced workflow management, including “closing the loop” functionality and a blockchain based immutable audit-trail.
  • Clinical Trials Intelligence has created an eco-system that fosters collaboration across the entire pharmaceutical industry while addressing the privacy and security concerns of all stakeholders.
  • A “first of it’s kind” perpetually increasing library of clinical data analytics that facilitates the sharing of “lessons learned” across corporate boundaries without any compromise of sensitive data.

One-Page Summary ClinTex Whitepaper Technical Paper

Pharmaceutical companies can now gain deep insight into the operational and clinical aspects of their trials without the necessity of major investment into backend technical infrastructure or data science expertise.

Key Features


A full history of clinical trial key metrics are stored immutably on Clinical Trials Intelligence’s decentralised ledger, where they are used by Clinical Trials Intelligence’s App’s to power bespoke predictive analytics algorithms in on-going trials on the platform.


As Clinical Trials Intelligence is a fully integrated platform that provides end-to-end auditable workflow management & oversight in trials, all actions, including preventative and corrective actions (CAPA), are recorded on the Clinical Trials Intelligence blockchain on an on-going basis.


This represents the creation of a clinical eco-system that enables interoperability and safe storage of all clinical trial data views, while also addressing the privacy and security concerns of all stakeholders.

CTi Applications

The CTi eco-system consists of seven separate Apps which each provide invaluable key insights and immense benefit to stakeholders such as Clinical Project Managers & Physicians, Clinical Data Managers, Pharmacovigilance staff and Site Monitors.



Operational Excellence

Provides intuitive operational oversight of clinical trials for clinical project managers, clinical data managers and remote staff, allowing instream decision-making on what actions are required to ensure a successful project.



Clinical Data Visualisations

Provides enhanced clinical data review through the use of data visualisations to identify issues that may impact on the trial integrity and safety of the patient e.g. data quality issues, disease exacerbation. Furthermore, CTi-CDV will facilitate flagging of these issues, and corrective actions to be recorded and monitored.



Predictive Analytics

The CTi-PDA application will combine all operational and clinical data sources and use predictive modelling to forecast issues and events before they happen. The CTi-PDA application will reveal hidden correlations across all datasets thereby facilitating the pharmaceutical company to take pro-active action to address.



Risk Based Monitoring

The CTi-RBM application will use current and historical data to predict specific risks, and thereby allow for tactical deployment of the pharmaceutical company’s data and site monitoring resources to take preventative action. This predictive risk based approach differs from current reactive approaches to risk and can significantly reduce site monitoring costs during a clinical trial.



Patient Recruitment and Retention

The CTi-PRR application manages recruitment and retention of patients for clinical trials by providing a portal for patient identification and producing a series of alerts (based on predictive analytics) that flag when a patient is at risk of withdrawing from the study.



Site Investigators

The CTi-SIM application manages the recruitment of investigators (physicians) to run clinical trials,and manages token payment compensation by the pharmaceutical company to investigators, triggered by data-driven milestones and KPIs, defined on Clinical Trials Intelligence.



Vendor Management

CTi-VMM provides oversight on data quality and manages token payment compensation by the pharmaceutical company to the third party vendors, triggered automatically by data-driven milestones and KPIs, defined on Clinical Trials Intelligence.

Our team

Combining the best of expertise from across the pharmaceutical, clinical, software development and data analytics spectrum.

Brendan O’Mainnin

Director of Operations

Brendan is a highly experienced project manager and business analyst with extensive experience in financial operations, telecommunications & consumer marketing. Successful proven leadership skills, he enjoys working with people to solve problems. Brendan has had an interest in the blockchain space since 2013 and intertwines this experience with his business expertise regularly in his role as a director in ClinTex.

Ethan Diamant

Director of Clinical Data Services

Ethan is leading the Clinical Trial Services function, responsible for building partnerships with the pharmaceutical industry, and ensuring that evolving customer requirements are built into ClinTex’s products and services. Ethan has 19 years experience working directly in clinical trials including clinical data monitoring, study optimization and global operational excellence.

Neill Barron

Director of Clinical Data Analytics

Neill leads the requirements specification, design and development of the CTi platform, ensuring it meets current and future real-world challenges for the pharmaceutical industry. He has over 20 years’ broad clinical development experience through a blend of senior roles in clinical data management, data analytics, technical/process improvement and site data monitoring.

Sean Flanagan

Head of Business Development

Sean has 12 years extensive experience in the Financial Services industry and brings to the team a valuable knowledge of corporate client management, wealth management and securitisation.. His track record in the cultivation of investor and client relations will help ClinTex deliver their development roadmap and generate value for all stakeholders.

John McCabe

Head of Legal & Regulatory

John holds a BA (Hons) in Business Law and is a licenced solicitor in England, Wales and Ireland after being admitted into the Law Society of Ireland in 2013. John has been working in law for over eleven years and has a keen interest in all things blockchain. He is excited to be bringing his focus to the cryptocurrency legal and regulatory landscape.

Ed Burke

Senior Developer

Edward earned his Master of Engineering (Meng) in Dublin City University in 2007 and boosts a wealth of software engineering experience from his 10+ years’ experience in senior design roles with companies such Paddy Power Better, Citi, and Fidelity. Ed specialises in C#, Java, Python and Solidarity and his strong focus and passion for scalable solutions makes him a most welcome addition to the ClinTex team.

Roman Tsivka

Blockchain Developer

Roman is an experienced blockchain architect specialising in Solidity, with rich experience in Ethereum smart contracts and distributed ledger technology. He has previously worked on the successful implementation of blockchain solutions within the public and private sectors, including extensive work with various Fortune 500 companies. Roman has responsibility for smart contract development, audit, and deployment within the CTi project.

Victoria Boychuk


Victoria is a qualified software engineer and has been working with Solidity since early 2018, when she took on her first Solidity Developer role with blockchain development agency, Applicature. As a member of the technical team, Victoria will support the design, development and roll-out of the CTi project through phases 1, 2 & 3.

Ian Arden

Blockchain Development Advisor

Ian is a partner at Applicature – a boutique Blockchain development agency focused on strategic consulting and implementation of Blockchain, smart contracts, ICO wallets and payment gateways and consumer applications. His expertise and experience in helping blockchain enterprises build and grow makes him a valuable advisor to the ClinTex team.

Sean Comiskey

Technology Engineering Advisor

Sean is highly motivated software engineer with experience covering the full software development life cycle, with particular specialisation in event sourcing and CQRS. He brings excellent understanding of modern software development principles, practices and paradigms to the ClinTex advisory board.

Dr. Samandip Dhesi

Medical Advisor

Samandip is a physician, entrepreneur and blockchain enthusiast. Through his work with Intellimed, a government-funded AI start-up working in partnership with the largest NHS Trust in the UK, and his academic connections, Samandip will advise the ClinTex team in relation to our collaborative research grant, giving the brightest post-graduate researchers the opportunity to access the ClinTex system and fund their projects.

Our partners


Intellimed is an innovative health-tech company focusing on streamlining UK National Health Service (NHS) processes, reducing costs and improving patient care. Intellimed is part of the Serendip Digital Health quarter based at the Innovation Birmingham Campus, and will be a valuable partner for CTi Platform deployments in healthcare and clinical research settings.

Global Blockchain Consortium

The GBC has been established with the mission of promoting blockchain awareness and education in the areas of fintech, disruptive tech and blockchain technologies. The GBC errand is to work in strategic collaboration with organisations and individuals that are revolutionising leading practices and wider adaptation of fintech and blockchain technologies elucidation to aid wider society.


Applicature are blockchain development agency and since 2010 have specialising in the development of smart contacts and the research, deployment, and customisation of tailored blockchain technology solutions.


Chainlink is decentralized oracle network that connects blockchain-based smart contracts to external data, payment networks, and various real-world events. Chainlink’s secure infrastructure allows smart contracts to link to APIs, in order to communicate with and obtain data from external sources such as Clinical Trial Management Systems (CTMS) and Electronic Data Capture (EDC) systems.

Sum & Substance

Sum & Substance are a pioneer in the Trusted Digital Identity space that specialise in identity proofing, risk-based authentication, regulatory identification, and the detection and prevention of the use of stolen identities, ensuring a robust and comprehensive risk and compliance solution.


Beosin is a well respected and experienced blockchain technology firm offering a full spectrum solution from tactical technical execution to high-level theoretical modelling, with a speciality in the auditing of smart contracts for blockchain projects.

Sterling Law

Sterling Law is a modern and innovative boutique law firm with cross-domain specialisation that allows for seamless solutions to solve complex problems.

CTi Development Roadmap

The development of Clinical Trials Intelligence from concept to completion.






Ideation & Research

Concept Development

Development Sprint 1 ‘Minimum Viable Product’
Whitepaper Published

Industry Consultation on CTi Prototype
Core Team Established

Sprint 2 ‘Enhancement’

Proof of Concept

Strategic Partnerships Agreed

CTi Data Model Finalised

CTi-OEM Prototype Development
Private Funding Rounds

CTi GUI Development

CTi-OEM Development
Public Token Sale

Blockchain Verification of CTi Pre-Processing Data

CTi-PDA Development

Migration on-chain of CTi Clinical Data Statistical Summaries
Industry Testing Pilot

CTi-PRR Development

CTi-RBM Development

CTi-CDV Development
Live Client On-Boarding Begins (1st Revenue)

Migration on-chain of the CTi Data Model and CTi Processing Engine

CTI-VMM Development

CTi-SIM Development