Quanterix Expands Laboratory Developed Test Menu with Launch of Neurofilament Light Chain Test
Quanterix Corporation (NASDAQ: QTRX) has announced the validation of a new CLIA blood test to quantitatively measure neurofilament light chain (NfL) levels in serum. This test aids in assessing neurodegenerative conditions and neuronal damage. NfL is a crucial biomarker for various neurological disorders, and the Simoa NfL test is widely recognized for its clinical relevance. The FDA previously granted Breakthrough Device designation for this test in relation to multiple sclerosis. This launch aims to enhance clinical diagnostics and support future therapeutic trials.
- Launch of a validated CLIA blood test for neurofilament light chain (NfL) measurement enhances diagnostic capabilities.
- NfL is a well-established biomarker with relevance across numerous neurological disorders, potentially increasing market adoption.
- FDA's Breakthrough Device designation may accelerate development and acceptance of the NfL test in clinical settings.
- None.
New CLIA blood test expands access to important “brain health” biomarker to advance research and clinical care
NfL is a well-studied biomarker for neuro-axonal injury with wide applicability to different neurological disorders. Any disorder or injuring force resulting in neuronal damage can lead to the release of NfL into the interstitial fluid and cerebrospinal fluid (CSF). A fraction of these proteins diffuses into the blood, where concentrations are typically 50- to 100-fold lower than in CSF and difficult to measure with conventional immunoassay technologies. Measurement of this protein in serum and plasma was first enabled with the release of the research use only (RUO) Simoa NfL kit several years ago.
Simoa NfL is the most widely published NfL test with hundreds of research papers demonstrating its validity for assessing neuronal damage, and it has become widely adopted in therapeutic clinical trial designs. Published research using the Simoa NfL test has shown correlations between increased serum NfL levels and neuronal injury across a range of disorders, including amyotrophic lateral sclerosis (ALS), Huntington’s disease, HIV infection, Parkinsonian disorders, traumatic brain injury (TBI), concussion, small vessel disease, Alzheimer’s disease, and multiple sclerosis (MS). Additionally, recent studies characterizing changes of blood NfL levels in normal aging populations have provided necessary reference range values to aid the interpretation of measurements from individuals being evaluated in clinical care settings. Simoa NfL measurements have supported approval of therapeutics, such as Novartis’ Kesimpta (ofatumumab) for MS, and have been used in a number of therapeutic trials related to Alzheimer’s disease, including Eisai’s lecanemab Phase 3 Clarity AD study, highlighted at the recent Clinical Trials for Alzheimer’s Disease (CTAD) conference.
Last year, the FDA granted Breakthrough Device designation for Quanterix’s NfL test as a prognostic aid in assessing the risk of disease activity in patients diagnosed with relapsing-remitting MS (RRMS). The FDA’s Breakthrough Device designation is granted to products that have the potential to offer more effective diagnosis or treatment of life-threatening diseases with an unmet medical need. The program is designed to enable accelerated development, assessment, and review processes, with the intention to provide patients with more timely access to breakthrough technologies or devices.
“Assessment and monitoring of brain health is incredibly difficult and typically performed in limited fashion by surgery or imaging. We see NfL as not only an important marker for neurodegenerative disease but also a critical measure of brain-related side effects during chemotherapy, CAR T-cell therapy, and stroke,” said
The Simoa NfL LDT will be offered through Quanterix’s
For more information about Quanterix’s work in neurology, visit: https://www.quanterix.com/therapeutic-areas/neurology/.
About
From discovery to diagnostics, Quanterix’s ultrasensitive biomarker detection is fueling breakthroughs only made possible through its unparalleled sensitivity and flexibility. The Company’s Simoa® technology has delivered the gold standard for earlier biomarker detection in blood, serum or plasma, with the ability to quantify proteins that are far lower than the Limit of Quantification (LoQ) of conventional analog methods. Its industry-leading precision instruments, digital immunoassay technology and CLIA-certified Accelerator laboratory have supported research that advances disease understanding and management in neurology, oncology, immunology, cardiology and infectious disease.
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FAQ
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