Welcome to our dedicated page for Veracyte news (Ticker: VCYT), a resource for investors and traders seeking the latest updates and insights on Veracyte stock.
Veracyte, Inc. (symbol: VCYT) is a pioneering genomic diagnostics company dedicated to significantly enhancing patient care through innovative diagnostic solutions. The company specializes in developing and providing genomic diagnostic products and services that improve clinical outcomes by resolving the uncertainties inherent in traditional diagnostic methods.
Veracyte's core business revolves around creating tests that offer more accurate diagnoses without resorting to risky, costly, and often unnecessary surgeries. By employing top-tier scientific rigor, state-of-the-art tools, and the brightest minds in the field, Veracyte delivers diagnostic solutions that bring clarity and assurance to patients and physicians alike.
The company's product portfolio includes the Afirma analysis, Percepta, Envisia, and other cutting-edge diagnostic tests. These products are designed to tackle diseases such as thyroid cancer, lung cancer, and idiopathic pulmonary fibrosis. Veracyte's diagnostic tests are distinguished by their ability to provide conclusive results where traditional methods fall short, thereby sparing patients from unnecessary surgical procedures.
Recent achievements highlight Veracyte's commitment to innovation and excellence. The company consistently introduces evidence that sets new standards in genomic tests, fundamentally altering current clinical practice norms. This commitment to scientific excellence ensures that Veracyte remains at the forefront of the genomic diagnostics industry.
Veracyte's impact extends beyond just clinical outcomes; it significantly influences the lives of both patients and physicians by offering a clearer path forward. Through continuous research, strategic partnerships, and an unwavering dedication to improving patient care, Veracyte stands out as a leader in the genomic diagnostics field.
Veracyte reported significant growth in Q4 2021, achieving $67.3 million in revenue, a 95% increase year-over-year. For the full year, total revenue reached $219.5 million, up 87%. However, operating expenses rose 104% to $227.0 million, primarily due to acquisition-related costs, leading to a net loss of $75.6 million, a 116% increase. The company anticipates 2022 revenue to be between $260 million and $275 million, marking a growth of 18% to 25%.
Veracyte, Inc. has appointed Annie McGuire as senior vice president and general counsel, effective immediately. McGuire, with extensive experience from Fortune 100 and healthcare companies, will manage the company's legal functions and report directly to CEO Marc Stapley. Previously, she was general counsel at Rakuten Medical and has held leadership positions at MyoKardia, where she played a key role in its $13 billion acquisition by Bristol Myers Squibb. Her appointment is anticipated to enhance Veracyte's strategic vision in diagnostics.
Veracyte, Inc. has appointed Jonathan Wygant as its new chief accounting officer, effective immediately. Wygant will manage all global accounting operations, financial reporting, and tax functions, reporting directly to Rebecca Chambers, the CFO. He previously held finance leadership roles at several healthcare companies, including as corporate controller at Biosplice Therapeutics. This leadership change aims to strengthen Veracyte's accounting operations as the company pursues its global strategic vision.
Veracyte, Inc. (Nasdaq: VCYT) will release its financial results for Q4 and full-year 2021 after market close on February 28, 2022. A conference call is scheduled at 4:30 p.m. ET to discuss these results and provide a general business update. Investors can access the conference call via the company's website, where a replay will also be available afterward. Veracyte is a diagnostics company focused on improving patient care through genomic tests for various cancers and diseases, leveraging advanced technology to expedite diagnosis and treatment.
Veracyte, Inc. (Nasdaq: VCYT) presented new data at the 2022 ASCO GU Symposium confirming the efficacy of the Decipher Prostate Genomic Classifier for prostate cancer treatment selection. This Phase 3 study validates the Classifier's role as a prognostic biomarker for men with intermediate-risk prostate cancer, providing critical insights for personalized treatment. Key findings indicate that patients classified as Decipher ‘high-risk’ have significantly worse clinical outcomes compared to ‘low-risk’ patients. This innovative approach could greatly enhance treatment strategies for prostate cancer patients.
Veracyte (Nasdaq: VCYT) announced that CEO Marc Stapley and CFO Rebecca Chambers will participate in a fireside chat at the 11th Annual SVB Leerink Global Healthcare Conference on February 16 at 2:20 p.m. Eastern Time. A live audio webcast of the presentation will be available on Veracyte’s website, with a replay accessible for 90 days afterward. Veracyte specializes in diagnostics, offering tests for various cancers and other diseases, utilizing genomic advancements to enhance patient care.
Veracyte (NASDAQ: VCYT) announced the presentation of six abstracts at the 2022 ASCO GU Cancers Symposium, occurring from
The event takes place in
Veracyte (NASDAQ: VCYT) has announced significant leadership promotions aimed at enhancing its strategic vision in diagnostics. Tina Nova, Ph.D., is appointed president of the CLIA U.S. business, while Stephane Debono becomes general manager for IVD and EMEA organizations. Giulia C. Kennedy, Ph.D., is named global chief scientific officer and chief medical officer. These appointments are expected to align Veracyte's operations and bolster its market presence. The company focuses on developing innovative diagnostic tests to address unmet clinical needs, ultimately improving patient outcomes globally.
Veracyte, Inc. (NASDAQ: VCYT) released clinical data supporting the Envisia Genomic Classifier's role in enhancing diagnostic and treatment processes for patients with idiopathic pulmonary fibrosis (IPF). The findings, published in the Annals of the American Thoracic Society, demonstrate a significant increase in IPF diagnoses (39%) and physician confidence (36.2%) post-Envisia application. The study emphasizes reduced reliance on invasive procedures while promoting timely treatment recommendations, with potential benefits for approximately 200,000 patients annually in the U.S. and Europe.