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Applied AT-001’s Phase 3 Miss | Lilly Does DTC January 8, 2024
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Together with
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“You think, ‘Why don’t more people do this?’ from a business standpoint. But from a medical standpoint, it does concern me.”
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Dr. Andrew Kraftson regarding Eli Lilly’s new direct-to-consumer platform for its Zepbound weight loss drug.
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Cardiology Pharmaceuticals
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Applied Therapeutics saw its shares fall 40% late last week after revealing that its diabetic cardiomyopathy drug candidate AT-001 (caficrestat) didn’t meet its phase 3 trial’s primary endpoint. However, the trial did show enough “encouraging results” for Applied to assert that AT-001 could still become the first diabetic cardiomyopathy treatment.
- Diabetic cardiomyopathy (DbCM) describes diabetes-associated changes in the structure and function of the heart’s myocardium, often leading to heart failure.
- AT-001 is an investigational oral Aldose Reductase inhibitor being developed for the treatment of diabetic cardiomyopathy.
- There are no other drugs specifically approved to treat DbCM, although some patients are prescribed SGLT2 inhibitors
The ARISE-HF phase 3 trial had 675 DbCM patients at high risk of progression to overt heart failure take either AT-001 or a placebo, as an add-on to standard diabetes therapies.
The study didn’t show statistically significant improvements or prevention of worsening DbCM (the primary endpoint) — the AT-001 and placebo groups had -0.01 and -0.31 ml/kg/min Peak VO2 declines over 15 months (p = 0.210).
However, there was some secondary silver linings:
- AT-001 achieved statistically significant improvements among the 62% of participants who weren’t also taking SGLT2 or GLP-1 inhibitors (+0.08 vs. -0.54 ml/kg/min Peak VO2).
- Far fewer participants in the AT-001 group experienced “clinically significant worsening in cardiac functional capacity” than the placebo group (32.7% vs. 46%).
- AT-001 was generally safe and well tolerated, as both groups had similar rates of serious adverse events and low incidence of treatment-related discontinuations.
These secondary outcomes were enough for Applied Therapeutics to call its results “encouraging” and position AT-001 as an “important potential tool for physicians in treatment of DbCM patients,” especially considering that DbCM patients still don’t have an approved therapy.
However, Applied Therapeutics is apparently more “encouraged”about its galactosemia drug govorestat, announcing plans to find a partner to bring AT-001 to approval and commercialization, so it can focus its resources on govorestat.
The Takeaway Although most headlines focused on Applied Therapeutics’s stock decline, and some folks on Twitter/X mocked its mention of “encouraging results,” the fact that AT-001 stabilized cardiac functional capacity (especially among those not on SGLT2 or GLP-1 inhibitors) might actually be encouraging for DbCM patients currently living without an approved therapy.
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Measuring True Cardiac Risk
How can AI help physicians “see” beyond conventional lipid profiles? Tune in to this on-demand webinar showcasing how Cleerly’s AI-QCT solution complements conventional approaches to evaluating heart disease risk factors, and improves coronary artery disease diagnosis and heart attack risk assessments.
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PIA’s Post-Processing Solution
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Where to Go for Cardio AI?
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- Lilly Goes DTC: Eli Lilly raised eyebrows and concerns across healthcare last week, with the launch of its LillyDirect platform, built to connect patients with an independent telehealth provider that would handle prescribing and delivering its Zepbound GLP-1 obesity med. Although LillyDirect doesn’t offer any financial advantages, it provides convenient access to the drug and should help convert more of Lilly’s web visitors into Zepbound users. Whether it will provide patients with similar care as traditional routes is another story.
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- Optimizing Diabetes HF Screening: A study of diabetes patients without ASCVD found that performing WATCH-DM score evaluations followed by selective NT-proBNP testing is clinically effective and economical for HF risk screening. In 4,889 diabetic patients without ASCVD, 6.2% developed HF over five years. Many of those patients who developed HF (85%) could be identified using a variety of two-step screening strategies, but performing selective NT-proBNP testing based on initial WATCH-DM risk scores was most cost effective.
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Ready to realize the benefits of cardiovascular imaging structured reporting? Check out these quick and powerful Change Healthcare videos detailing the efficiency gains provided by structured reporting and what it takes to drive adoption.
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A Milestone Study for Cardiac Strain Analysis
Us2.ai’s deep learning algorithm was able to interpret echo AI left ventricular strain images with similar accuracy as conventional measurements. Read all about this milestone study and its implications for echo strain access in EHJ-Digital Health.
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- Advancing CAD Risk Assessments: When HeartFlow used its Plaque Analysis solution to analyze more than 11,000 CCTAs in the DECODE Study, the solution achieved 95% agreement with IVUS and led to changes in two out of every three patients’ treatment plans. See how HeartFlow Plaque Analysis can help you accurately assess your patients’ CAD risks and personalize their treatment.
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