PROLUNG IS NOW IONIQ SCIENCES

A Modern Approach to
Cancer Testing

IONIQ Sciences is at the forefront of early cancer detection

Cancer is a scourge on society. One in two Americans will be diagnosed with cancer during their lifetime and one in five will die. The five-year cancer survival rates approach 90% when diagnosed in the earliest stages of the disease versus less than 10% in the latest stages. 

We believe it doesn’t have to be this way. 

Expanding from a Single Cancer
Test to a
Multi-Cancer Screen

Early detection saves lives and money by detecting cancer at its earliest, most-treatable stages. We are well-positioned to develop a multi-cancer screen by leveraging our lung test, breast test, proprietary technology, substantial EIA database, and our deep clinical experience.

IONIQ Development Pipeline

ProLung Test (Lung Cancer)
Breast Cancer Test
Multi-Cancer Screen

Clinical Data

Assembled a deep clinical evidence library with data collected from more than 1,200 subjects

Premier Clinical Sites

More than 20 premier cancer institutions around the world participated in our clinical trials

Awarded Breakthrough Device Designation

IONIQ's ProLung Test was awarded “Breakthrough Device Designation” by US FDA for its life-enhancing potential

Intellectual Property

Robust, growing intellectual portfolio of patents and know-how

15 yrs
in the Making

IONIQ Recent News

BioUTAH highlights IONIQ Science’s recent accomplishments

Our life sciences industry partner, BioUTAH, published a nice article on their website that highlights some of our recent accomplishments. Follow the link below to read it and learn more about BioUTAH. BioUtah is an independent, non-profit 501(c)(6) trade association serving the life sciences community

IONIQ Sciences announces institutional offering

IONIQ Sciences announces institutional offering Salt Lake City, UT, May 28, 2020 – IONIQ Sciences Inc. (“IONIQ Sciences” or the “Company”), announced it is initiating an institutional private equity offering on the heels of receiving ‘Breakthrough Device Designation’ from the U.S. FDA for its lung

Standards & Certifications

Meet the Team