AVIM therapy shows promise for managing hypertension in high-risk elderly patients, addressing unmet needs in cardiovascular care.
Quiver AI Summary
Orchestra BioMed Holdings, Inc. presented key insights on its atrioventricular interval modulation (AVIM) therapy for managing high-risk hypertension at the CSI 2025 Meeting. The therapy aims to address hypertensive heart disease, which affects over 7.7 million U.S. patients, particularly those with diastolic dysfunction and the potential progression to heart failure with preserved ejection fraction (HFpEF). Dr. Daniel Burkhoff highlighted AVIM therapy as a novel device-based approach designed to lower blood pressure and improve cardiovascular function in this at-risk population, which currently has limited treatment options. The presentation also discussed the BACKBEAT global pivotal study evaluating AVIM therapy in patients with uncontrolled hypertension who require a dual-chamber pacemaker. Orchestra BioMed continues to pursue partnerships and collaborations to advance this promising approach in hypertension management, as it has recently received FDA Breakthrough Device Designation for the therapy.
Potential Positives
- Presentation at a significant medical conference (CSI 2025) underscores the clinical potential of AVIM therapy for treating high-risk hypertension, positioning Orchestra BioMed as a key player in cardiovascular innovations.
- AVIM therapy received FDA Breakthrough Device Designation, highlighting its promise in addressing unmet medical needs in managing hypertension, particularly in older patients with heart disease.
- The ongoing BACKBEAT pivotal study aiming to evaluate AVIM therapy further validates its potential efficacy and safety, providing a pathway for future commercial success.
- The collaboration with Medtronic, a leader in cardiac pacing therapy, enhances credibility and potential market reach of AVIM therapy within the medical device sector.
Potential Negatives
- Potential overemphasis on AVIM therapy's benefits may lead to skepticism if clinical outcomes do not meet expectations in ongoing studies.
- The reliance on Breakthrough Device Designation for commercial success could pose a risk if regulatory challenges arise in future approvals.
- Limited therapeutic options mentioned for managing hypertensive heart disease may highlight the risks involved in the current treatment landscape that AVIM therapy aims to address.
FAQ
What is AVIM therapy designed to treat?
AVIM therapy is designed to manage blood pressure in high-risk hypertension patients, especially those with hypertensive heart disease.
Who presented the clinical insights on AVIM therapy?
Dr. Daniel Burkhoff, Director of Heart Failure Research at Cardiovascular Research Foundation, presented the insights at the CSI 2025 Meeting.
What is the significance of AVIM therapy's FDA Breakthrough Device Designation?
The Breakthrough Device Designation highlights the potential of AVIM therapy to meet unmet needs in treating uncontrolled hypertension.
What data was discussed regarding the efficacy of AVIM therapy?
The presentation discussed data showing significant reductions in both ambulatory and office blood pressure in patients treated with AVIM therapy.
What ongoing study is focused on AVIM therapy?
The BACKBEAT study is evaluating the safety and efficacy of AVIM therapy in patients with uncontrolled hypertension who need a pacemaker.
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.
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Wall Street analysts have issued reports on $OBIO in the last several months. We have seen 3 firms issue buy ratings on the stock, and 0 firms issue sell ratings.
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- H.C. Wainwright issued a "Buy" rating on 04/23/2025
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Full Release
- 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”)
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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;
- The growing body of clinical and mechanistic evidence 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
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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 Contact
Silas Newcomb
Orchestra BioMed
[email protected]
Media Contact
Kelsey Kirk-Ellis
Orchestra BioMed
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