Daxor Corporation announces studies validating its BVA technology, reducing hospital readmissions and enhancing survival in heart failure patients.
Quiver AI Summary
Daxor Corporation announced significant advancements in its blood volume measurement technology, highlighted by three studies presented at the Heart Failure Society of America (HFSA) Annual Scientific Meeting. The studies demonstrated that Daxor's next-generation BVA analyzer significantly improves patient outcomes in heart failure management, particularly by reducing hospital readmissions and boosting survival rates. Key findings included that patients with optimized blood volume had no unplanned admissions, compared to high admission rates for those with imbalances. Additionally, BVA-guided care improved survival and reduced complications among patients undergoing LVAD implantation, while diagnosing conditions like Cardiac Amyloidosis. With these developments, Daxor is well-positioned to expand its market presence in the vital healthcare sector focused on blood management and patient care.
Potential Positives
- Significant clinical data presented at a reputable conference validates that Daxor’s BVA technology can lead to zero unplanned hospital admissions for patients with optimal blood volume, indicating potential for enhanced patient care.
- The successful debut of the next-generation BVA analyzer, which received FDA clearance, suggests strong market demand and positions Daxor for growth in a multi-billion-dollar healthcare market.
- The studies demonstrated substantial improvements in patient outcomes, including increased survival rates and reduced readmissions, which can lead to cost savings in healthcare.
- Daxor's ISO certification and advanced manufacturing capabilities position the company for accelerated market expansion and increased operational efficiencies.
Potential Negatives
- Concerns about the company's reliance on forward-looking statements may create uncertainty among investors regarding actual market performance and product adoption.
- The press release hints at potential risks in post-market clinical data collection and the necessity for increased market and physician acceptance, which may indicate challenges ahead.
- Any fluctuation in FDA regulatory actions could adversely impact Daxor's business operations and market share, as noted in the forward-looking statements section.
FAQ
What is the main benefit of Daxor's BVA technology?
Daxor's BVA technology significantly reduces hospital readmissions and improves survival rates in heart failure patients through precise blood volume measurement.
How does the BVA analyzer enhance patient care?
The BVA analyzer provides real-time, accurate data that helps clinicians make individualized treatment decisions, optimizing patient management and outcomes.
What clinical findings were presented regarding heart failure care?
Clinical data showed that patients with optimal blood volume as measured by BVA had zero unplanned hospital admissions compared to 57-77% for others.
How has the BVA technology impacted LVAD procedures?
BVA-guided care during LVAD procedures improved survival rates and reduced critical complications such as severe acute kidney injury and readmissions.
What distinguishes Daxor in the healthcare market?
Daxor combines 50 years of experience with innovative, FDA-cleared technology that accurately measures blood volume, addressing a critical healthcare challenge.
Disclaimer: This is an AI-generated summary of a press release distributed by GlobeNewswire. The model used to summarize this release may make mistakes. See the full release here.
$DXR Insider Trading Activity
$DXR insiders have traded $DXR stock on the open market 1 times in the past 6 months. Of those trades, 1 have been purchases and 0 have been sales.
Here’s a breakdown of recent trading of $DXR stock by insiders over the last 6 months:
- MICHAEL RICHARD FELDSCHUH (Chief Executive Officer) purchased 2,063 shares for an estimated $16,277
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$DXR Hedge Fund Activity
We have seen 2 institutional investors add shares of $DXR stock to their portfolio, and 2 decrease their positions in their most recent quarter.
Here are some of the largest recent moves:
- OSAIC HOLDINGS, INC. added 8,750 shares (+inf%) to their portfolio in Q2 2025, for an estimated $85,662
- MORGAN STANLEY added 3,468 shares (+3986.2%) to their portfolio in Q2 2025, for an estimated $33,951
- UBS GROUP AG removed 326 shares (-100.0%) from their portfolio in Q2 2025, for an estimated $3,191
- RENAISSANCE TECHNOLOGIES LLC removed 100 shares (-0.4%) from their portfolio in Q2 2025, for an estimated $978
- JPMORGAN CHASE & CO added 0 shares (+0.0%) to their portfolio in Q2 2025, for an estimated $0
- SBI SECURITIES CO., LTD. added 0 shares (+0.0%) to their portfolio in Q2 2025, for an estimated $0
- KEYES, STANGE & WOOTEN WEALTH MANAGEMENT, LLC added 0 shares (+0.0%) to their portfolio in Q2 2025, for an estimated $0
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Full Release
Three Studies Validate BVA-Guided Care Significantly Cuts Hospital Readmissions and Boosts Survival in High-Cost Heart Failure Segments
OAK RIDGE, TN, Sept. 30, 2025 (GLOBE NEWSWIRE) -- Daxor Corporation (Nasdaq: DXR), the global leader in blood volume measurement technology , today announces significant commercial momentum and clinical validation following the Heart Failure Society of America (HFSA) Annual Scientific Meeting. The company’s successful debut of its newly FDA-cleared, next-generation BVA analyzer signals a new era of data-driven fluid management for a multi-billion-dollar market .
The initial response from clinicians confirmed robust market demand for the new system, driven by its enhanced ease of use, speed, and over 95% accuracy .
New Clinical Data Validates Commercial Opportunity
During the meeting, new clinical data presented from three leading institutions further validated Daxor’s BVA technology across critical, high-cost patient populations :
- Banner University Medical Center ( Heart Failure Care): New data confirms the urgent need for a focus on "volume re-calibration" in heart failure care. Patients with optimal total blood and red cell volume as measured by Daxor's BVA test had zero unplanned hospital admissions , versus 57-77% for those with imbalances in either total blood or red blood cell volume. These findings prove objective BVA measurement reveals patients needing additional treatment to prevent readmissions
- Wellstar Health System (Left-Ventricular Assist Device (LVAD) Implantation) : The use of BVA-guided care pre- and post-LVAD implantation led to remarkable outcome improvements. The study showed substantially reduced severe acute kidney injury, one of the leading complications from LVAD procedures. Quantified results demonstrated this approach boosted 30-day survival from 90.3% to 93.6% and 1-year survival from 79.6% to 87.8%; cut 30-day readmissions from 28.6% to 18.5% ; and decreased post-operative length of stay by 1.5 days
- Geisinger Medical Center (Cardiac Amyloidosis): New data confirms that patients with Cardiac Amyloidosis (CA) have significantly higher total blood and plasma volumes. BVA can help diagnose this unique CA phenotype, assisting clinicians with accurate diuretic dosing for better patient function
“The data presented at HFSA, particularly the clinical findings showing zero unplanned readmissions for optimally managed patients, provides undeniable evidence that BVA is an essential diagnostic for improving care and reducing costs ,” said John L. Jefferies, MD, MPH, MBA, Chief Medical Officer of Daxor Corporation. “Coupling this overwhelming clinical validation with our faster, more accessible analyzer means Daxor is now ideally positioned to capture a significant commercial share of this multi-billion-dollar market .”
About Daxor Corporation
Daxor Corporation (NASDAQ: DXR) is tackling healthcare's "multi-billion-dollar silent crisis", the inability to precisely measure blood volume. This often results in suboptimal care, prolonged hospital stays, and increased readmissions for many high-cost medical conditions like heart failure and those requiring ICU care. With 50 years of experience and innovation, Daxor is proud to manufacture and distribute its patented, FDA-cleared Blood Volume Analysis (BVA) diagnostic which offers unmatched, real-time, precise data via its rapid, hand-held, lab-based system. This empowers clinicians to make individualized treatment decisions that significantly improve patient outcomes and deliver substantial efficiencies in value-based healthcare. Daxor is ISO certified and operates a U.S.-based, 20,000-square-foot state-of-the-art manufacturing facility, positioning the company for accelerated market expansion.
For more information, please visit our website at Daxor.com .
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Forward-Looking Statements
Certain statements in this release may include forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including without limitation, statements regarding the impact of hiring sales staff and expansion of our distribution channels. Forward-looking statements are predictions, projections and other statements about future events that are based on current expectations and assumptions and, as a result, are subject to risks and uncertainties. Many factors could cause actual future events to differ materially from the forward-looking statements in this release, including, without limitation, those risks associated with our post-market clinical data collection activities, benefits of our products to patients, our expectations with respect to product development and commercialization efforts, our ability to increase market and physician acceptance of our products, potentially competitive product offerings, intellectual property protection, FDA regulatory actions, our ability to integrate acquired businesses, our expectations regarding anticipated synergies with and benefits from acquired businesses, and additional other risks and uncertainties described in our filings with the SEC. Forward-looking statements speak only as of the date when made. Daxor does not assume any obligation to publicly update or revise any forward-looking statements, whether as a result of new information, future events or otherwise.
Investor Relations Contact:
Bret Shapiro
COO – Head of Capital Markets
COREIR
(561)-479-8566-Cell
[email protected]
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www.coreir.com