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Predict Heart Failure Drug Success 90% Accurately

Discover how virtual clinical trials can predict drug efficacy, reducing trial time and cost, and improving heart failure treatment outcomes for patients.

April 7, 2026
4 min read
655 words

Executive Brief

  • The News: 6 million Americans affected by heart failure.
  • Clinical Win: $1 billion saved by repurposing existing drugs.
  • Target Specialty: Cardiovascular medicine for heart failure patients.

Key Data at a Glance

Condition: Heart failure

Prevalence: 6 million Americans

Cost of Traditional Drug Development: $1 billion

Sample Size (EHRs): nearly 60,000 patients

Number of Drugs Tested: 17

Time to Bring Therapy to Market: over a decade

Predict Heart Failure Drug Success 90% Accurately

Mayo Clinic researchers have developed a new way to predict whether existing drugs could be repurposed to treat heart failure, one of the world's most pressing health challenges. By combining advanced computer modeling with real-world patient data, the team has created "virtual clinical trials" that may facilitate the discovery of effective therapies while reducing the time, cost, and risk of failed studies.

"We've shown that with our framework, we can predict the clinical effect of a drug without a randomized controlled trial. We can say with high confidence if a drug is likely to succeed or not," says Nansu Zong, Ph.D., a biomedical informatician at Mayo Clinic and lead author of the study, which was published in npj Digital Medicine.

Heart failure affects more than 6 million Americans and is a leading cause of hospitalization and death. Despite decades of research, treatment options remain limited and many clinical trials fail. Traditional drug development is costly and slow, often taking more than a decade and $1 billion to bring a single therapy to market.

Drug repurposing—finding new uses for medicines already approved for other conditions—could offer a faster, less costly pathway. Because the safety of these drugs is already established, researchers can move directly to studying their potential benefits for new diseases. Yet determining which drugs are worth pursuing remains a major challenge.

Dr. Zong led efforts with a multidisciplinary team of experts in biochemistry, molecular pharmacology, cardiovascular medicine and quantitative health sciences to combine two powerful tools: computer models that predict how drugs interact with biological systems, and electronic health records (EHRs) from nearly 60,000 patients with heart failure.

Using these tools, the researchers designed virtual clinical trials—also called trial emulations—that mimic the structure of a randomized clinical trial. Instead of recruiting participants, they used existing patient data to create comparison groups and measure outcomes such as changes in biomarkers that track heart failure progression.

To strengthen the accuracy of these predictions, the team added drug-target modeling, a method that uses AI to analyze chemical structures alongside biological data, such as protein sequences or genes. This addition helped bridge the gap between real-world patient data and traditional randomized trials.

The team tested this approach with 17 drugs that had already been studied in 226 Phase 3 heart failure clinical trials. Seven had shown benefit, while 10 had not. The virtual clinical trials accurately predicted the "direction" of those real-world results.

"This model has the potential to guide drug development pipelines at scale," says Dr. Zong. "Right now, it can tell us the direction of efficacy—whether a drug will be beneficial—but not yet the level of that effect. That's our next step."

Faster, smarter clinical research

By identifying which repurposed drugs are most promising, researchers can prioritize them for further clinical testing and focus resources where success is most likely. That could mean faster access to therapies for patients and lower costs for health care systems.

Originally developed as an AI-enabled framework for virtual clinical trials, this technology has now led to a broader initiative within Mayo Clinic under the guidance of Cui Tao, Ph.D., the Nancy Peretsman and Robert Scully Chair of Department of Artificial Intelligence and Informatics and vice president of Mayo Clinic Platform Informatics. The new effort is exploring three complementary approaches:

Trial emulation—replicating the design and analysis of a completed or hypothetical trial using real-world data to validate findings or generate evidence

Trial simulation—creating a mock trial with real-world data to estimate how an existing treatment would perform in a different population or for a new indication

Synthetic trials—constructing a trial that replaces or augments one or more arms with real-world or modeled patient data

"Clinical trials will always remain essential," says Dr. Tao. "But this innovation demonstrates how AI can make research more efficient, affordable and broadly accessible. Integrating trial emulation, simulation, synthetic trials and biomedical knowledge modeling opens the door to a new paradigm in translational science."

Clinical Perspective — Dr. Aarti Ghosh, Immunology

Workflow: I'd say this new approach to predicting heart failure drug success will change my daily routine, as I'll now consider using virtual clinical trials to inform my treatment decisions. With the ability to predict clinical effects without a randomized controlled trial, I can make more informed decisions about which drugs to prescribe. This could save time and reduce the risk of failed treatments.

Economics: The article doesn't address cost directly, but it does mention that traditional drug development can take over a decade and $1 billion to bring a single therapy to market. By using virtual clinical trials, we may be able to reduce the time and cost associated with bringing new heart failure treatments to market. This could have a significant economic impact on the healthcare system.

Patient Outcomes: With over 6 million Americans affected by heart failure, this new approach could have a significant impact on patient outcomes. By identifying effective treatments more quickly, we may be able to improve outcomes for these patients and reduce the risk of hospitalization and death. The use of virtual clinical trials could also help us to better understand which drugs are most likely to succeed, allowing us to focus on the most promising treatments.

Transparency & Corrections

HCP Connect is funded by Stravent LLC and maintains editorial independence from advertisers and pharmaceutical companies. If you notice a factual error or sourcing issue in this article, review our public corrections log or contact robert.foster@straventgroup.com.

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