Kitea Health
Overview
Executive Summary
Kitea Health is revolutionising hydrocephalus management with the Kitea System, a wireless, implantable brain pressure monitoring device. Our technology, backed by over 20 years of research and $15 million in grants, aims to reduce unnecessary hospital visits and improve patient outcomes. With a total addressable market of $2 billion in the US alone, Kitea Health is seeking $10 million in investment to fund pivotal trials and secure FDA approval.
Problem and Solution
Hydrocephalus is a life-threatening condition affecting over a million people in the US, with 50% of shunts failing within the first 2 years. Shunts are recognised to have the highest failure rate of any medical device. Kitea Health's solution, the Kitea System, offers real-time, remote monitoring of intracranial pressure, enabling early intervention and reducing false alarms.
Highlights & Milestones
- Fully developed technology with proven biocompatibility and performance in animals.
- Strong IP portfolio with filed patents, including wireless power and data communication technologies.
- First human clinical trial commenced in NZ in June 2024. Adult enrolment complete, children now underway. US trial approval expected in late 2025.
- Total addressable market of $2 billion for hydrocephalus, with potential for expansion into cardiac monitoring markets.
Market Opportunity
Hydrocephalus affects an estimated 6.4 million people globally, with 1 million in the US alone. The Kitea System addresses a significant market need, with potential to reduce healthcare costs and improve patient outcomes.
Competitive Advantage
- Unique technology as the world's smallest brain implant, offering remote monitoring and minimal surgical impact.
- Wireless, long-term monitoring with high accuracy and MRI compatibility.
- Cost savings through reduced ED visits and improved patient outcomes.
Exit Strategy
Kitea Health aims to file for FDA approval in 2027, positioning the company for acquisition by larger medical device companies. This strategic exit will leverage our technology for global impact.
Use of Funds
- Complete First-In-Human Trials in in children in NZ.
- Secure FDA Investigational Device Exemption (IDE) for US trials.
- Scale device manufacturing to meet growing demand.
We invite you to explore our full deal room for more detailed information and to join us in transforming hydrocephalus management
Highlights & Milestones
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Problem and Solution
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Exit Strategy
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Market Opportunity
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Vivamus maximus nulla volutpat, ornare lorem a, vulputate enim. In dui nisl, vestibulum eu finibus pretium, eleifend et eros. Vivamus in venenatis risus, ut dictum velit. Praesent rhoncus tempor fermentum. In malesuada tellus eu volutpat posuere. Nullam ut dignissim libero, ut pharetra leo. Nullam sit amet aliquam felis. Suspendisse volutpat ante eget tincidunt feugiat. Nunc placerat sapien et metus molestie, in viverra augue viverra. Donec varius metus ut arcu vestibulum hendrerit. Sed viverra risus neque, ac commodo enim lacinia at.
Morbi posuere tortor vitae sapien faucibus auctor. Donec nulla ipsum, aliquet non bibendum sit amet, viverra non metus. Sed blandit efficitur orci, id dignissim eros.
Donec sollicitudin massa ut tellus gravida, ut luctus lacus maximus. Maecenas porttitor a tellus ac sagittis. Suspendisse potenti. Donec mauris sem, tristique a ipsum vitae, pretium facilisis libero. Nullam interdum mauris in euismod pretium. Class aptent taciti sociosqu ad litora torquent per conubia nostra, per inceptos himenaeos. Nunc felis lectus, ornare a nunc eu, convallis suscipit elit. Donec at magna non orci maximus mollis. Cras commodo venenatis lectus vel fringilla.
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