logo
Orchestra BioMed Showcases AVIM Therapy as Purpose-Built Solution for Hypertensive Heart Disease at CSI Frankfurt 2025

Orchestra BioMed Showcases AVIM Therapy as Purpose-Built Solution for Hypertensive Heart Disease at CSI Frankfurt 2025

Business Upturn4 hours ago

Presentation underscores unique potential for atrioventricular interval modulation ('AVIM') therapy to manage blood pressure in older, high-risk patients who have indicators of diastolic dysfunction and progression to heart failure with preserved ejection fraction ('HFpEF')
Hypertensive heart disease represents over 7.7 million U.S. patients, the same population with hypertension and elevated cardiovascular risk cited in the recent FDA Breakthrough Device Designation ('BDD') for AVIM therapy
NEW HOPE, Pa., June 18, 2025 (GLOBE NEWSWIRE) — Orchestra BioMed Holdings, Inc. (Nasdaq: OBIO, 'Orchestra BioMed' or the 'Company'), a biomedical company accelerating high-impact technologies to patients through risk-reward sharing partnerships, today announced the presentation of key clinical insights into the role of AVIM therapy for the treatment of high-risk hypertension at the Congenital, Structural, and Valvular Heart Disease Interventions ('CSI') 2025 Meeting. The data highlight AVIM therapy's unique potential to address hypertensive heart disease, a significant and under-recognized cardiovascular syndrome that affects a growing segment of the aging hypertension population.
The talk, 'Atrioventricular Interval Modulation (AVIM) Therapy for Hypertension and HFpEF,' will be delivered by Daniel Burkhoff, M.D., Ph.D., Director of Heart Failure, Hemodynamics and Mechanical Circulatory Support Research at Cardiovascular Research Foundation and clinical advisor to Orchestra BioMed. Dr. Burkhoff will spotlight the clinical utility of AVIM therapy as a novel, device-based approach to blood pressure management designed specifically for patients with hypertensive heart disease. This population has increased risk for major adverse cardiac events and currently lacks sufficient therapeutic options. The presentation will take place on June 18, 2025, at 3:33pm CEST / 9:33am ET as part of the ' Interventions for Chronic Heart Failure ' session.
Dr. Burkhoff commented, 'Hypertensive heart disease is not a singular diagnosis, but a high-risk cardiovascular syndrome driven by longstanding, uncontrolled high blood pressure which significantly increases the likelihood of adverse clinical outcomes such as stroke, myocardial infarction, diastolic dysfunction and progression to heart failure. The data I will review at CSI explore how AVIM therapy may offer a unique treatment specifically catered to this group of patients leveraging a mechanism of action designed to reduce cardiac preload and modulate autonomic nervous system responses to reduce blood pressure and improve cardiovascular function. This represents a potential paradigm shift in how we approach blood pressure management using tailored interventions designed to directly impact the complex pathophysiology of high-risk hypertension.'
The presentation will cover: The clinical burden and therapeutic gaps in managing patients with high-risk hypertension and increased risk of heart failure;
in managing patients with high-risk hypertension and increased risk of heart failure; The growing body of clinical and mechanistic evidence demonstrating AVIM therapy's potential to lower blood pressure and improve cardiac function; and
demonstrating AVIM therapy's potential to lower blood pressure and improve cardiac function; and Details on the BACKBEAT global pivotal study, currently enrolling patients with uncontrolled hypertension who are indicated for a dual-chamber pacemaker. The study is being conducted in collaboration with Medtronic, the global leader in cardiac pacing therapy.
'AVIM therapy was purpose-built to address the complex and underserved needs of patients with hypertensive heart disease, a subgroup often overlooked by conventional therapy,' said Avi Fischer, M.D., Senior Vice President of Medical Affairs and Innovation at Orchestra BioMed. 'As a programmable, pacemaker-integrated solution, AVIM therapy has the potential to fit seamlessly into existing electrophysiology practices while opening the door to better outcomes in a large, underserved population. Dr. Burkhoff's presentation at CSI Frankfurt further reinforces the growing clinical interest in AVIM therapy and highlights the significant opportunity to transform care of hypertensive heart disease, especially given our recently granted BDD status, which applies directly to this patient profile.'
About Orchestra BioMed
Orchestra BioMed (Nasdaq: OBIO) is a biomedical innovation company accelerating high-impact technologies to patients through risk-reward sharing partnerships with leading medical device companies. Orchestra BioMed's partnership-enabled business model focuses on forging strategic collaborations with leading medical device companies to drive successful global commercialization of products it develops. Orchestra BioMed's lead product candidate is AVIM therapy for the treatment of hypertension, the leading risk factor for death worldwide. Orchestra BioMed is also developing Virtue SAB for the treatment of atherosclerotic artery disease, the leading cause of mortality worldwide. Orchestra BioMed has a strategic collaboration with Medtronic, one of the largest medical device companies in the world, for development and commercialization of AVIM therapy for the treatment of hypertension in pacemaker-indicated patients, and a strategic partnership with Terumo, a global leader in medical technology, for development and commercialization of Virtue SAB for the treatment of artery disease. The Company has received four Breakthrough Device Designations from the U.S. FDA across these two core programs, reflecting the significant potential of its technologies to address high unmet needs in cardiovascular care. For further information about Orchestra BioMed, please visit www.orchestrabiomed.com , and follow us on LinkedIn .
References to Websites and Social Media Platforms
References to information included on, or accessible through, websites and social media platforms do not constitute incorporation by reference of the information contained at or available through such websites or social media platforms, and you should not consider such information to be part of this press release.
About AVIM Therapy
AVIM therapy is an investigational therapy compatible with standard dual-chamber pacemakers designed to substantially and persistently lower blood pressure. It has been evaluated in pilot studies in patients with hypertension who are also indicated for a pacemaker. MODERATO II, a double-blind, randomized pilot study, showed that patients treated with AVIM therapy experienced net reductions of 8.1 mmHg in 24-hour ambulatory systolic blood pressure (aSBP) and 12.3 mmHg in office systolic blood pressure (oSBP) at six months when compared to control patients. In addition to reducing blood pressure, clinical results using AVIM therapy demonstrate improvements in cardiac function and hemodynamics. The BACKBEAT (BradycArdia paCemaKer with atrioventricular interval modulation for Blood prEssure treAtmenT) global pivotal study will further evaluate the safety and efficacy of AVIM therapy in lowering blood pressure in patients who have systolic blood pressure above target despite anti-hypertensive medication and who are indicated for or have recently received a dual-chamber cardiac pacemaker. AVIM therapy has been granted Breakthrough Device Designation by the FDA for the treatment of uncontrolled hypertension in patients who have increased cardiovascular risk.
Forward-Looking Statements
Certain statements included in this press release that are not historical facts are forward-looking statements for purposes of the safe harbor provisions under the United States Private Securities Litigation Reform Act of 1995. Forward-looking statements generally are accompanied by words such as 'believe,' 'may,' 'will,' 'estimate,' 'continue,' 'anticipate,' 'intend,' 'expect,' 'should,' 'would,' 'plan,' 'predict,' 'potential,' 'seem,' 'seek,' 'future,' 'outlook' and similar expressions that predict or indicate future events or trends or that are not statements of historical matters. These forward-looking statements include, but are not limited to, statements relating to the enrollment, implementation and design of the Company's planned and ongoing pivotal trials, realizing the clinical and commercial value of the Company's product candidates, the potential safety and efficacy of the Company's product candidates, and the ability of the Company's partnerships to accelerate clinical development. These statements are based on various assumptions, whether or not identified in this press release, and on the current expectations of the Company's management and are not predictions of actual performance. These forward-looking statements are provided for illustrative purposes only and are not intended to serve as and must not be relied on as a guarantee, an assurance, a prediction, or a definitive statement of fact or probability. Actual events and circumstances are difficult or impossible to predict and may differ from assumptions. Many actual events and circumstances are beyond the control of the Company. These forward-looking statements are subject to a number of risks and uncertainties, including changes in domestic and foreign business, market, financial, political, and legal conditions; risks related to regulatory approval of the Company's commercial product candidates and ongoing regulation of the Company's product candidates, if approved; the timing of, and the Company's ability to achieve expected regulatory and business milestones; the impact of competitive products and product candidates; and the risk factors discussed under the heading 'Item 1A. Risk Factors' in the Company's Annual Report on Form 10-K for the year ended December 31, 2024, which was filed with the SEC on March 31, 2025 and the risk factor discussed under the heading 'Item 1A. Risk Factors' in the Company's Quarterly Report on Form 10-Q for the quarterly period ended March 31, 2025, which was filed with the SEC on May 12, 2025.
The Company operates in a very competitive and rapidly changing environment. New risks emerge from time to time. Given these risks and uncertainties, the Company cautions against placing undue reliance on these forward-looking statements, which only speak as of the date of this press release. The Company does not plan and undertakes no obligation to update any of the forward-looking statements made herein, except as required by law.
Investor ContactSilas NewcombOrchestra BioMed
[email protected]

Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

AventaMed, a KARL STORZ Company, Receives Expanded Indication for Solo+ Tympanostomy Tube Device (TTD)
AventaMed, a KARL STORZ Company, Receives Expanded Indication for Solo+ Tympanostomy Tube Device (TTD)

Business Wire

time29 minutes ago

  • Business Wire

AventaMed, a KARL STORZ Company, Receives Expanded Indication for Solo+ Tympanostomy Tube Device (TTD)

EL SEGUNDO, Calif.--(BUSINESS WIRE)--KARL STORZ United States is proud to announce that the US Food and Drug Administration (FDA) has cleared an expanded indication for the AventaMed Solo+™ Tympanostomy Tube Device (TTD), allowing its use in pediatric patients aged 6 months and older. This expanded clearance builds on the previous 510(k) clearance, which was indicated for patients 6 to 24 months old. The Solo+™ Tympanostomy Tube Device (TTD) has received expanded clearance from the FDA. The Solo+ device represents a significant advancement in pediatric ENT care. It is intended to deliver a tympanostomy tube (also known as a ventilation tube) into a patient's tympanic membrane, or eardrum, to treat problems arising from ear infections. Traditionally, this procedure would be performed in an operating room under general anesthesia. The Solo+ device offers a convenient alternative. Using as little as a topical anesthetic, the Solo+ device integrates multiple functions into a single, user-friendly instrument, deploying the tube with the press of a button. As a result, it enables tympanostomies to be performed in an office setting. New clinical findings support the safe and effective use of the Solo+ device, showing that physicians were consistently able to complete the procedure in the office as intended—without needing to move to the operating room. The Solo+ Tympanostomy Tube Device demonstrated consistent, reliable performance across pediatric age groups, with strong follow-up outcomes. These results provide both guardians and physicians with greater confidence in selecting an office-based approach to ear tube placement for a wider range of children. 'On behalf of patients and their families, we are excited by this expanded indication,' said Chris Smith, VP of Sales & Marketing, Head & Neck Division, at KARL STORZ US. 'This makes it possible to offer this effective treatment to a broad population. With clear advantages like avoiding general anesthesia, reducing total procedural costs, and delivering high patient satisfaction, the Solo+ device will benefit doctors and patients alike. It's part of our commitment to provide technology that addresses real-world needs.' About Ear Infections Chronic ear infections are a leading reason for doctor visits among young children. 1-3 Children are more susceptible to this potentially painful condition, which can adversely affect the ability to hear. 1 Treatment often involves procedures known as myringotomy and tympanostomy. Myringotomy involves making an incision in the eardrum to drain excess fluid from the middle ear. It is sometimes performed as a standalone treatment, but is often combined with tympanostomy, in which a tiny tube is inserted in the eardrum to alleviate pressure and allow fluid to drain. The procedure is common: by the age of three, nearly 1 in every 15 children will have had ear tubes. 3 About KARL STORZ Since its founding in Germany in 1945, KARL STORZ has grown to become a leading global supplier of endoscopy solutions, including imaging and integration across all sites of care. Now in its third generation, the family-owned company employs 9,400 people in more than 40 countries worldwide. The company acquired the Solo+ technology through the acquisition of AventaMed, which was spun off from Munster Technological University in 2015. For more information, visit 1 Ahmed S et al. Incremental health care utilization and costs for acute otitis media in children. Laryngoscope. 2014;124(1):301-5. doi: 10.1002/lary.24190. 2 Bhattacharyya N, Shay SG. Epidemiology of Pediatric Tympanostomy Tube Placement in the United States. Otolaryngol Head Neck Surg. 2020;163(3):600-602. doi: 10.1177/0194599820917397. 3 Rosenfeld RM et al. Clinical Practice Guideline: Tympanostomy Tubes in Children. Otolaryngol Head Neck Surg. 2013;149:S1-S35. doi: 10.1177/0194599813487302.

Is Salmon Skin Safe to Eat?
Is Salmon Skin Safe to Eat?

Health Line

time30 minutes ago

  • Health Line

Is Salmon Skin Safe to Eat?

Salmon skin is generally safe to eat and offers health benefits, like decreasing the chance of heart disease. But some exceptions exist. You may need to consider factors like individual health or where the salmon is from. Salmon is both delicious and nutritious. In addition to being a source of protein, it provides omega-3 fatty acids, vitamins B and D, and minerals like niacin and phosphorus. Many people looking to substitute red meat in their meals turn to salmon for its health properties. While some people like to remove the skin before cooking a fillet of salmon, others swear by leaving the skin on and eating it for an additional health benefit. Health benefits The skin of a salmon, like the flesh, contains high amounts of long-chain omega-3 fatty acids. There's strong evidence that these fatty acids can reduce triglyceride levels and decrease your chances of heart disease. Cooking fillets with the skin on can also keep nutrients and oils inside the salmon itself that might otherwise be lost in the preparation process. Salmon is one of the fish that the U.S. Food and Drug Administration (FDA) recommends eating two to three times per week for health benefits. Safe forms and doses Much of the world's salmon supply has been contaminated by environmental pollution. But when it comes to human exposure, these toxins have a cumulative effect. That means that it's still generally safe to consume salmon and salmon skin in conservative amounts. It's also important to pay attention to where your salmon comes from. The FDA, with the help of the Environmental Protection Agency (EPA), has compiled recommendations to advise people how to consume fish safely. The most contaminated fish is farmed from the Atlantic Ocean. Wild-caught salmon from the Atlantic is slightly less contaminated. If your salmon was caught in the Atlantic Ocean, it might be best to avoid eating its skin. The best kind of salmon skin to cook and eat would come from a wild-caught Pacific salmon. Risks and side effects Salmon skin is generally safe for people to eat. However, fish are known to be contaminated by pollutants in our air and water. Chemicals called polychlorinated biphenyls (PCBs) can be absorbed by salmon during their life through their skin and in other fish that they eat. PCBs are a known carcinogen and have been linked to birth defects. Methylmercury is also absorbed by salmon during their lifetime. These chemicals can be toxic to humans when consumed in large amounts. Pregnant woman are especially prone to experiencing negative side effects from these toxins, and might even pass them to their unborn child. Methylmercury has also been linked to birth defects. Parents may also want to be wary of the effects of these toxins on their young children. A 19 95 study found that skinned salmon from the Great Lakes area had 50 percent fewer pesticides than salmon with the skin on. Takeaway If you're a pregnant or nursing woman, you may want to avoid salmon skin altogether to be on the safe side. For most other people, the benefits of eating salmon skin will probably outweigh the risks for if the salmon comes from uncontaminated waters. Salmon skin can be cooked by itself, apart from the flesh of the fish, to make tasty recipes you might never have tried before. Crispy fried salmon skin has a similar texture to bacon, but without many of the health concerns associated with that high-sodium pork product. And baked salmon skin can be broken apart to serve as a salad garnish (think croutons without carbs!), used in sushi, or eaten as is for a healthy snack.

Kansas City Celebrates UMKC Carnegie R1 Status at Union Station
Kansas City Celebrates UMKC Carnegie R1 Status at Union Station

Yahoo

time33 minutes ago

  • Yahoo

Kansas City Celebrates UMKC Carnegie R1 Status at Union Station

Community leaders came together to celebrate impact research milestone will have for region Kansas City Skyline with Union Station in Forefront Kansas City Community Leaders Celebrate Kansas City, MO, June 18, 2025 (GLOBE NEWSWIRE) -- Federal, state, county, city, business and university leaders gathered at Union Station to celebrate the University of Missouri-Kansas City's designation as a Carnegie Research 1 university. They spoke about the economic impact of this national designation for the Kansas City community, Missouri and beyond. State Representative Melissa Douglas recognized the university's milestone with a state resolution, and Kansas City Mayor Quinton Lucas recognized it with a city proclamation. UMKC achieved Carnegie Research 1, or R1, designation earlier this year. The designation reflects university-wide dedication to research, innovation and community collaboration. Of all four-year institutions in the United States, only 6% are R1 and UMKC is the only one in Kansas City. The R1 designation elevates the academic prestige of UMKC, providing more opportunities for faculty and students through recruitment and research grants. UMKC researchers demonstrated research at Union Station including drones, nursing simulations and more. This designation isn't just a milestone for the university; the benefits will echo through the community and beyond. Prestigious faculty and research grants will bring new jobs and opportunities into the region. The research happening at UMKC makes an impact of more than $300 million to the greater Kansas City area each year. Additionally, the university's research activity annually brings an estimated 2,000 jobs to the area. Leaders expressed excitement about what this means for our region: Charlie Shields, chair of Greater Kansas City Chamber of Commerce, president and CEO of University Health and UMKC Trustee: 'UMKC research advances our safety as a society and our health and wellbeing – impacts I see every day at University Health. UMKC is leading the way in key areas of research, including electromagnetic radiation and energy, advanced and critical materials, unmanned platforms, cybersecurity and digital humanities.' U.S. Representative Mark Alford: 'What UMKC is doing in the defense and security space has already led to the creation of private businesses and jobs and has massive potential for continued growth. This milestone only further helps expand on what could have a massive economic impact on the Midwest, creating business and jobs in the region that help our country receive the materials it needs from areas in Kansas and Missouri.' State Representative Melissa Douglas: 'I see UMKC serving in healthcare throughout the state of Missouri, not only at its Health Sciences Campus in Kansas City, but through its satellite campuses to serve rural Missourians. As UMKC continues to expand its healthcare outreach throughout the state of Missouri, I know we'll see more needed research to improve the lives of all Missourians. Together, we have built a hub of intellectual vitality that will have benefits for years to come.' Kansas City Mayor Quinton Lucas: 'I'm quite familiar with the good works at UMKC, and grew up with it, as my mother worked there. I've seen the city and the university grow together to become world class, and this important R1 designation is a testament to that.' Jackson County Executive Frank White: 'I've seen up close how UMKC research can help communities. Our Healthy Jackson County truly made a difference to so many people's lives. And UMKC's community-participatory research truly makes a difference to so many people's lives.' UMKC Student Government Association President Justice Horn: 'This isn't just a title. It's a transformation. For students, it means expanded opportunities, greater visibility and stronger preparation for our futures. It's a game changer—and a sign that UMKC is investing in discovery, innovation and real-world impact right here in the Kansas City community.' UMKC Chancellor Mauli Agrawal: 'This moment reflects the work of an entire community that believes in the power of education, research and partnership to shape a better future for all of us. And it reflects a university that has long been deeply embedded in the life of this city – from healthcare and entrepreneurship to science, the arts and urban development.' Tim Cowden, President and CEO of the Kansas City Area Development Council: 'This R1 status helps elevate our brand to the world. Kansas City's status is rising. The R1 designation is a welcome mat to talent not just in the Kansas City area, but around the world.' Celebrations continued as buildings around the city lit up in recognition of the university's Carnegie Research 1 status. Union Station, Children's Mercy, Saint Luke's Hospital, Country Club Plaza, City Hall, KC Wheel and Power and Light Building were illuminated UMKC blue and gold. Read more about UMKC's Carnegie R1 impact, including a roundtable discussion among two dozen regional leaders, at Attachments Kansas City Skyline with Union Station in Forefront Kansas City Community Leaders Celebrate CONTACT: Stacy Downs UMKC 8162351441 downs@ in to access your portfolio

DOWNLOAD THE APP

Get Started Now: Download the App

Ready to dive into the world of global news and events? Download our app today from your preferred app store and start exploring.
app-storeplay-store