What’s Next in Obstructive Hypertrophic Cardiomyopathy Treatment?

There’s no cure for obstructive hypertrophic cardiomyopathy (oHCM) — treatments focus on symptom management and preventing complications. But the landscape is changing, and more cutting-edge therapies are on the way.
“This is a hopeful time to be a patient who has limiting symptoms. People have so many more options on the table now, and so many more that are coming down the pike that are really worthwhile,” says Sara Saberi, MD, an assistant professor in the division of cardiovascular medicine at the University of Michigan in Ann Arbor.
Here’s what you may be able to expect in the next 5 to 10 years, plus what you can do to access cutting-edge oHCM treatments today.
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7 Ways to Manage Obstructive Hypertrophic Cardiomyopathy Symptoms
More Cardiac Myosin Inhibitors
Sodium-Glucose Cotransporter 2 Inhibitors
Sarcomere Modulators
While cardiac myosin inhibitors encourage the heart to squeeze out blood or contract normally, a sarcomere modulator helps the heart fill with blood the way that it’s supposed to. “It basically acts to improve the heart muscle’s relaxation phase,” explains Dr. Saberi.
Less-Invasive Surgeries
Surgery for oHCM has become much less common since cardiac myosin inhibitors came onto the scene. But it’s still needed in some cases, and emerging procedures could make surgery easier and lower risk.
Gene Therapy
While these are exciting treatments that could potentially cure oHCM, “We’re at the very beginning with gene therapy, with the first few patients participating in phase I clinical trials,” says Owens. In order for gene therapy to become an approved treatment, many more years of research will be needed.
Clinical Trials
You may be a candidate for a clinical trial if advanced therapies like mavacamten or aficamten haven’t done enough to control your oHCM symptoms. To learn more about your options, you can research ongoing trials at ClinicalTrials.gov and talk with your cardiologist about which ones may be a good fit for you.
The Takeaway
- New medications for oHCM — cardiac myosin inhibitors like mavacamten and aficamten — target the disease more directly than ever before, and additional drugs in this class are in development.
- Several other promising drug classes are in the pipeline, including SGLT2 inhibitors and sarcomere modulators, which may improve heart function in different ways and could expand treatment options in the coming years.
- Less-invasive surgical techniques to septal myectomy are being developed to avoid open-heart surgery while still effectively removing excess heart muscle, which may reduce risk and recovery time.
- Gene therapy, which could one day address the root genetic causes of oHCM, holds long-term potential but remains in the earliest stages of research.
Resources We Trust
- Mayo Clinic: Hypertrophic Cardiomyopathy and Treatment Options
- Hypertrophic Cardiomyopathy Association: Myosin Inhibitors
- American Heart Association: Hypertrophic Cardiomyopathy (HCM)
- European Society of Cardiology: New Drugs in Hypertrophic Cardiomyopathy
- Cleveland Clinic: REMS Update: Mavacamten Still Effective in Treating Real-World Patients With HCM
- FDA Approves New Drug to Improve Heart Function in Adults With Rare Heart Condition. U.S. Food & Drug Administration. April 29, 2022.
- FDA Approves Drug to Improve Functional Capacity and Symptoms in Adults With Rare Inherited Heart Condition. U.S. Food & Drug Administration. December 23, 2025.
- Myosin Inhibitors. Hypertrophic Cardiomyopathy Association.
- New Drugs in Hypertrophic Cardiomyopathy. European Society of Cardiology. March 3, 2026.
- Kukowa A et al. Cardiac Myosin Inhibitors in the Treatment of Hypertrophic Cardiomyopathy: Clinical Trials and Future Challenges. Biomolecules. July 29, 2025.
- Ding C et al. SGLT-2 Inhibitors Improve Cardiac Function in Hypertrophic Cardiomyopathy: A Real-World Propensity Score-Matched Study. Frontiers in Cardiovascular Medicine. February 12, 2026.
- A Study to Evaluate the Efficacy and Safety of Sotagliflozin in Symptomatic Obstructive and Non-obstructive Hypertrophic Cardiomyopathy (SONATA-HCM). ClinicalTrials.gov. February 27, 2026.
- Chu EL-W et al. Emerging Pharmacological and Invasive Therapies for Hypertrophic Cardiomyopathy with Obstructive Physiology. Cardiac Failure Review. November 3, 2025.
- First-in-Human Transapical Beating-Heart Septal Myectomy in Patients With Hypertrophic Obstructive Cardiomyopathy. Journal of the American College of Cardiology. August 15, 2023.
- Wang S et al. Minimally Invasive Electro Septal Myectomy for Hypertrophic Obstructive Cardiomyopathy Through a Right Infra-Axillary Incision. Annals of Thoracic Surgery. October 17, 2025.
- Perez-Asensio A et al. A New Era in the Management of Hypertrophic Cardiomyopathy. Reviews in Cardiovascular Medicine. October 30, 2025.

Cheng-Han Chen, MD, PhD, FACC, FSCAI
Medical Reviewer
Cheng-Han Chen, MD, PhD, is the medical director of the structural heart program at MemorialCare Saddleback Medical Center in Laguna Hills, California, and director of structural a...

Marygrace Taylor
Author
Marygrace Taylor is an award-winning freelance health and wellness writer with more than 15 years of experience covering topics including women’s health, nutrition, chronic conditi...