Welcome to our dedicated page for Lantheus Holding news (Ticker: LNTH), a resource for investors and traders seeking the latest updates and insights on Lantheus Holding stock.
Lantheus Holdings, Inc. (NASDAQ: LNTH) is a radiopharmaceutical-focused company whose news flow centers on diagnostic imaging products, radiopharmaceutical pipeline progress and corporate developments. The company describes its purpose as enabling clinicians to "Find, Fight and Follow" disease, and its announcements frequently highlight advances in PET radiodiagnostics, oncology imaging agents and Alzheimer’s disease diagnostics.
News about Lantheus often covers regulatory milestones for its radiopharmaceutical pipeline. Recent releases include U.S. Food and Drug Administration (FDA) acceptance of a New Drug Application for a new formulation of its piflufolastat F 18 PSMA PET imaging agent, a PDUFA date for LNTH-2501 (Ga 68 edotreotide) for somatostatin receptor-positive neuroendocrine tumors, and FDA acceptance of an NDA for MK-6240, a tau-targeted PET imaging agent for Alzheimer’s disease. These updates provide insight into how the company is expanding its diagnostic portfolio in oncology and neurology.
Lantheus news also frequently addresses business development and portfolio shaping. The company has reported acquisitions of Evergreen Theragnostics and Life Molecular Imaging, adding assets such as OCTEVY and Neuraceq and expanding its capabilities across the radiopharmaceutical value chain. It has also announced the divestiture of its SPECT business to SHINE Technologies, along with licensing agreements such as an exclusive deal with GE HealthCare to develop, manufacture and commercialize PYLARIFY in Japan.
Investors and healthcare professionals following LNTH news can also expect quarterly earnings releases, stock repurchase program announcements, leadership transition updates and conference participation notices. Together, these items provide context on Lantheus’ financial performance, capital allocation, governance and strategic direction in the radiopharmaceutical and medical imaging space.
Lantheus Holdings announced that its subsidiary, EXINI Diagnostics AB, received FDA 510(k) clearance for its digital application, aPROMISE™, designed for prostate cancer imaging. This AI-based software enhances efficiency and consistency in PSMA PET/CT assessments, utilizing deep learning algorithms trained on over 3,000 images. The application is intended for healthcare professionals to improve the quantification and reporting of prostate cancer lesions. This follows the recent FDA approval of PYLARIFY®, a PSMA-targeted PET imaging agent, enhancing Lantheus's prostate cancer diagnostic capabilities.
Lantheus Holdings, Inc. (LNTH) reported Q2 2021 revenue of $101.1 million, marking a 53.1% increase from Q2 2020. However, the company posted a GAAP net loss of $26.7 million, compared to $7.0 million in the prior year. Adjusted EPS slightly rose to $0.11 from $0.10. Free Cash Flow jumped to $23.2 million, an increase of approximately $27.6 million year-over-year. The FDA approved PYLARIFY, enhancing their product portfolio. Revised guidance for FY 2021 estimates revenue between $395 million and $402 million.
Lantheus Holdings, Inc. (NASDAQ: LNTH) will host a conference call and webcast on July 28, 2021, at 8:00 a.m. ET to discuss its Q2 2021 financial and operational results. Investors can join the call by dialing U.S. 1-866-498-8390 or international 1-678-509-7599, using passcode 6149638. The live webcast will be accessible on the company's website, with a replay available after the call and archived for 30 days. Lantheus specializes in innovative imaging diagnostics and therapeutics, offering a broad product portfolio, including DEFINITY®, PYLARIFY®, and RELISTOR®.
Lantheus Holdings (NASDAQ: LNTH) announced data from the CONDOR pivotal trial on piflufolastat F 18 (18F-DCFPyL), presented at the Virtual Society of Nuclear Medicine and Molecular Imaging meeting. Dr. Steven Rowe from Johns Hopkins University delivered an oral presentation on June 15, 2021, analyzing disease detection rates and positive predictive values (PPV) in men with biochemically recurrent prostate cancer. The trial revealed high PPV and median detection rates for various anatomic regions, validating PYLARIFY's efficacy in detecting metastatic lesions.
Lantheus has received FDA approval for PYLARIFY, the first PSMA-targeted PET imaging agent for prostate cancer, marking a major advancement in oncology diagnostics. The agent enhances detection of suspected metastasis and recurrence, enabling timely treatment decisions. PYLARIFY is anticipated to be available across the U.S. by year-end following its immediate rollout in select regions. The approval is supported by pivotal studies showing high specificity and localization rates, making PYLARIFY a vital tool for managing prostate cancer.
Lantheus Holdings (NASDAQ: LNTH) announced a poster presentation of data from its Phase 3 CONDOR study at the ASCO Virtual Meeting from June 4-8, 2021. The session will focus on PSMA-targeted imaging in patients with biochemically recurrent prostate cancer, highlighting the correct localization rate and positive predictive value.
Presenter Frederic Pouliot, M.D., Ph.D., from CHU de Québec-Université Laval will showcase abstract No. 5023. Lantheus is a leader in imaging diagnostics and therapeutics, providing a broad portfolio aimed at serious medical conditions.
Lantheus Holdings (NASDAQ: LNTH) has announced that Mary Anne Heino, President and CEO, along with Bob Marshall, CFO, will present at the Jefferies Virtual Healthcare Conference on June 3 at 10:30 a.m. ET. Investors can access the live webcast of the presentation on the Company’s website. A replay will be available for 30 days post-event. Lantheus is a leader in imaging diagnostics and therapeutics, providing products like DEFINITY® and RELISTOR® to address serious medical conditions.
Lantheus Holdings (NASDAQ: LNTH) reported Q1 2021 revenue of $92.5 million, marking a 2.0% increase from Q1 2020. Net income rose to $9.0 million, equivalent to $0.13 per diluted share, compared to $3.3 million or $0.08 last year. However, adjusted diluted EPS fell 86.3% to $0.05 from $0.36. Operating cash flow was $9.8 million, and free cash flow increased to $7.3 million.
The company updates its FY 2021 revenue guidance to $390 million - $400 million and Q2 revenue between $93 million - $97 million.
EXINI Diagnostics AB, a subsidiary of Lantheus Holdings (NASDAQ: LNTH), has received CE Mark clearance for its AI-based software, aPROMISE, in Europe. This innovative tool enhances quantitative assessment of PSMA PET/CT in oncology, demonstrating a high reproducibility with an intraclass correlation coefficient of 0.99. aPROMISE aims to improve efficiency and accuracy in imaging assessments, particularly in detecting prostate cancer. With potential U.S. approval expected later this year, aPROMISE is designed to strengthen Lantheus's portfolio and assist clinicians in patient management.
Lantheus Holdings (NASDAQ: LNTH) announced a collaboration with Allegheny Health Network (AHN) to develop a treatment for xerostomia using Lantheus' microbubbles combined with AHN's ultrasound-assisted non-viral gene transfer (UAGT) technology. Xerostomia, often caused by cancer treatments, leads to severe dry mouth and related health issues. The partnership aims to leverage UAGT's potential for long-term xerostomia relief, with Lantheus supplying microbubbles. AHN will handle the development and commercialization of the treatment.