We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

Features Partner Sites Information LinkXpress hp
Sign In
Advertise with Us
PURITAN MEDICAL

Download Mobile App




PHASE Scientific and Lumos Diagnostics Partner on Rapid POC Test for Bacterial Respiratory Infection

By LabMedica International staff writers
Posted on 21 Jul 2025

A critical gap exists in the diagnosis of respiratory infections, which are often difficult to distinguish quickly and accurately as either bacterial or non-bacterial in origin. More...

This challenge has led to widespread overuse of antibiotics, a key contributor to antimicrobial resistance (AMR), which is a growing threat to public health and a driver of unnecessary healthcare costs. Clinicians are often forced to make treatment decisions without rapid diagnostic support, particularly in urgent and emergency care settings. The lack of point-of-care solutions that can differentiate infection types contributes to inefficient triage, delays in care, and inappropriate prescribing. Now, a rapid point-of-care test that distinguishes between bacterial and non-bacterial respiratory infections can improve antimicrobial stewardship and clinical decision-making across the U.S.

PHASE Scientific (Hong Kong, China) has entered into an exclusive U.S. distribution agreement with Lumos Diagnostics (Carlsbad, CA, USA) for FebriDx, a first-in-class rapid test that aids in the diagnosis of bacterial acute respiratory infection and differentiation from non-bacterial etiology in approximately 10 minutes using a single drop of blood. FebriDx from Lumos Diagnostics will become part of PHASE Scientific’s INDICAID portfolio, which is known for its high-quality, accessible rapid diagnostics. The test uses a unique combination of C-reactive protein (CRP) and Myxovirus resistance protein A (MxA) biomarkers to aid diagnosis. Its lateral flow format requires only a fingerstick blood sample and is designed to deliver results in about 10 minutes. FebriDx was validated in a pivotal clinical study, which showed that integrating the test into care can reduce unnecessary antibiotic use, improve patient outcomes, and lower healthcare costs. It enables faster, more informed treatment decisions in urgent and outpatient care settings.

A CLIA waiver study is currently progressing, with completion and application submission expected within the next three months. The product has received FDA 510(k) clearance, and the pending CLIA waiver application will broaden access to outpatient settings. FebriDx supports antimicrobial stewardship by helping clinicians reduce inappropriate prescribing and streamline clinical workflows. The solution is expected to expand significantly in the U.S. market, supported by PHASE Scientific’s proven commercial distribution network, which has delivered over 100 million diagnostic tests. The test targets a market opportunity of approximately USD 1.5 billion. Future efforts include expanding FebriDx’s accessibility through regulatory approval and further strengthening its integration into routine point-of-care diagnostics.

"We are thrilled to partner with Lumos, a company that shares our commitment to shaping the future of healthcare through innovation and collaboration, and support them with our scalable go-to-market strength in North America," said Dr. Ricky Chiu, Founder and CEO of PHASE Scientific. "A powerful complement to our INDICAID respiratory portfolio, FebriDx is a first-in-class diagnostic that perfectly aligns with our mission to bring fast, actionable diagnostics to the frontlines of care. We are confident this will unlock synergistic opportunities, further advancing our impact on antimicrobial stewardship and clinical decision-making across the U.S. As we continue to expand the INDICAID brand, we remain dedicated to strengthening our leadership in point-of-care solutions, empowering clinicians, and improving access to high-quality healthcare."

"This distribution agreement reflects a pivotal moment in Lumos' evolution,” said Doug Ward, CEO of Lumos Diagnostics. “We look forward to working with the PHASE Scientific team to ensure that FebriDx secures adoption in the U.S. market, delivering tangible clinical and financial value to the broader healthcare system. This agreement also validates the value of the FebriDx technology and provides a clear pathway to the U.S. market, which we expect will accelerate rapidly should we receive a grant for CLIA waiver from the FDA.”

Related Links:
PHASE Scientific
Lumos Diagnostics


Gold Member
Flocked Fiber Swabs
Puritan® Patented HydraFlock®
3-Part Differential Hematology Analyzer
Swelab Alfa Plus Sampler
New
HBV DNA Test
GENERIC HBV VIRAL LOAD VER 2.0
New
PSA Assay
CanAg PSA EIA
Read the full article by registering today, it's FREE! It's Free!
Register now for FREE to LabMedica.com and get access to news and events that shape the world of Clinical Laboratory Medicine.
  • Free digital version edition of LabMedica International sent by email on regular basis
  • Free print version of LabMedica International magazine (available only outside USA and Canada).
  • Free and unlimited access to back issues of LabMedica International in digital format
  • Free LabMedica International Newsletter sent every week containing the latest news
  • Free breaking news sent via email
  • Free access to Events Calendar
  • Free access to LinkXpress new product services
  • REGISTRATION IS FREE AND EASY!
Click here to Register








DIASOURCE (A Biovendor Company)

Channels

Molecular Diagnostics

view channel
Image: EvoLiver is the first test to receive FDA Breakthrough Device Designation in five years in the liver cancer surveillance space (Photo courtesy of Mursla Bio)

Patient-Friendly Blood Test to Transform Liver Cancer Surveillance

Hepatocellular carcinoma (HCC), the most common form of primary liver cancer, is the fastest-growing cause of cancer-related deaths. Although clinical guidelines recommend routine surveillance for high-risk... Read more

Hematology

view channel
Image: CitoCBC is the world first cartridge-based CBC to be granted CLIA Waived status by FDA (Photo courtesy of CytoChip)

Disposable Cartridge-Based Test Delivers Rapid and Accurate CBC Results

Complete Blood Count (CBC) is one of the most commonly ordered lab tests, crucial for diagnosing diseases, monitoring therapies, and conducting routine health screenings. However, more than 90% of physician... Read more

Immunology

view channel
Image: CellLENS enables the potential precision therapy strategies against specific immune cell populations in the tissue environment (Photo courtesy of MIT)

New AI System Uncovers Hidden Cell Subtypes to Advance Cancer Immunotherapy

To produce effective targeted therapies for cancer, scientists need to isolate the genetic and phenotypic characteristics of cancer cells, both within and across different tumors. These differences significantly... Read more

Technology

view channel
Image: The Check4 gene-detection platform (Photo courtesy of IdentifySensors)

Electronic Biosensors Used to Detect Pathogens Can Rapidly Detect Cancer Cells

A major challenge in healthcare is the early and affordable detection of serious diseases such as cancer. Early diagnosis remains difficult due to the complexity of identifying specific genetic markers... Read more
Copyright © 2000-2025 Globetech Media. All rights reserved.