Quanterix to Participate in the 15th Clinical Trials on Alzheimer’s Disease (CTAD) Task Force


BILLERICA, Mass.–()–Quanterix Corporation (NASDAQ: QTRX), a company fueling scientific discovery through ultrasensitive biomarker detection, today announced plans to participate in the upcoming 15th Clinical Trials on Alzheimer’s Disease (CTAD) Task Force in San Francisco, California from November 29 to December 2, 2022. Quanterix CEO Masoud Toloue is scheduled to present on Tuesday, November 29 at 9:55 a.m. PST, along with a panel of assay industry leaders, on leveraging the use of blood-based biomarkers rather than the current gold standard of positron emission tomography (PET). PET is an expensive testing modality, whereas less invasive, less expensive blood-based biomarkers have demonstrated promise to facilitate more efficient clinical trial enrollment and as a convenient monitoring test of drug treatment effects. The Task Force panel will also include perspectives from the pharmaceutical industry and academia.

“The field of Alzheimer’s disease diagnostics and therapeutics has become one of the most exciting areas in all of medical research. This year’s CTAD meeting promises to accelerate the excitement!” said Michael Weiner, MD, Professor of Radiology and Biomedical Imaging, Medicine, Psychiatry, and Neurology, UCSF, and President of the CTAD22 Scientific Committee.

CTAD is a meeting focused on Alzheimer’s disease therapeutic trials where key leaders in Alzheimer’s disease research from industry and academia form partnerships with the goal of speeding the development of effective treatments to fight the disease. Readouts from several Phase III clinical trials will be presented at this year’s meeting.

“Researchers in the pharmaceutical industry and academia continue to prove the importance of highly sensitive blood-based biomarker tests including pTau-181 and pTau-217, both of which have shown utility in recent Phase III trials,” said Masoud Toloue, CEO at Quanterix. “These assays represent an important breakthrough in Alzheimer’s disease therapeutics research, enabling more efficient trial designs focused on patients at earlier stages of disease, and potentially a convenient method of monitoring patients for response to the drugs. Quanterix has been at the forefront of this research, and we are excited to continue to support the momentum in the fight against Alzheimer’s disease at CTAD.”

For more information about Quanterix’s work with neurology, please visit https://www.quanterix.com/therapeutic-areas/neurology/.

About Quanterix

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. Quanterix has been a trusted partner of the scientific community for nearly two decades, powering research published in more than 2,000 peer-reviewed journals. Find additional information about the Billerica, Massachusetts-based company at https://www.quanterix.com or follow us on Twitter and LinkedIn.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Words such as “may,” “will,” “expect,” “plan,” “anticipate,” “estimate,” “intend” and similar expressions (as well as other words or expressions referencing future events, conditions or circumstances) are intended to identify forward-looking statements. Forward-looking statements in this news release are based on Quanterix’ expectations and assumptions as of the date of this press release. Each of these forward-looking statements involves risks and uncertainties. Factors that may cause Quanterix’ actual results to differ from those expressed or implied in the forward-looking statements in this press release are discussed in Quanterix’ filings with the U.S. Securities and Exchange Commission, including the “Risk Factors” sections contained therein. Except as required by law, Quanterix assumes no obligation to update any forward-looking statements contained herein to reflect any change in expectations, even as new information becomes available.





Read More: Quanterix to Participate in the 15th Clinical Trials on Alzheimer’s Disease (CTAD) Task Force

2022-11-16 13:30:00

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