Novartis came out with the results from the phase II Paramount study showing that the investigational compound LCZ696 is the first therapy to significantly reduce a key predictor of morbidity and mortality in patients with a condition called heart failure with preserved ejection fraction (HF-PEF). This difficult-to-treat disease affects up to half of the 20 million people with heart failure in Europe and the US. The data were presented at the ESC Congress 2012 (European Society of Cardiology) in Munich, Germany, and published simultaneously in The Lancet.
The results show that after 12 weeks, LCZ696 met its primary endpoint by reducing NT-proBNP[*] – a marker of stress on the heart and a predictor of patient outcomes – significantly more than valsartan. The data also suggest that LCZ696 may reverse some structural changes to the heart, that occur in patients with heart failure.
“These phase II results show that this novel treatment approach has the potential to reduce stress to the heart and to reduce enlargement of the left atrium of the heart, which occurs in patients with heart failure. So far no treatment has been shown to reduce morbidity and mortality in patients with HF-PEF. The favourable effects seen in this study are encouraging, and further testing of LCZ696 is warranted in this patient population,” said Dr Scott Solomon, Professor of Medicine at Harvard University and Director of Noninvasive Cardiology at Brigham and Women’s Hospital in Boston, US.
Heart failure (HF) is a disease in which the heart is unable to supply enough blood to meet the body’s needs. There are two common types: heart failure with preserved ejection fraction (HF-PEF) and heart failure with reduced ejection fraction (HF-REF). In patients with HF-PEF, the percentage of blood pumped out of the heart (also called the ejection fraction) remains within the normal range, but the heart does not relax enough to pump effectively. This results in structural changes that progressively weaken the heart leading to a range of debilitating symptoms. Patients with HF-PEF also commonly have other conditions such as hypertension, diabetes and atrial fibrillation.
Tim Wright, Global Head of Development, Novartis Pharma said, “The results of the Paramount study are promising for patients with HF-PEF as there is no effective treatment currently available. We believe that thanks to its novel mode of action and these positive study results, LCZ696 could significantly benefit people living with chronic heart failure. These results support our commitment to heart failure patients at every stage of their disease through our ongoing programme of clinical trials.”
LCZ696 is the first in a new class of medicines called angiotensin receptor neprilysin inhibitors (ARNIs). It works in a different way to existing heart failure treatments by inhibiting an enzyme (neprilysin, or NEP) in order to promote the body’s protective mechanisms, and blocking receptors involved in the narrowing of blood vessels (angiotensin receptors). LCZ696 therefore acts simultaneously on two important pathways in the development of the disease.
The Paramount study showed that after 12 weeks of treatment, reduction in NT-proBNP was 23 per cent greater with LCZ696 than valsartan (p=0.005). In addition, there was a greater reduction (p=0.003) in left atrial size (cardiac remodelling) in LCZ696-treated patients at the end of the 36-week study. This suggests that LCZ696 could provide an effective treatment for patients with HF-PEF. The study also showed that LCZ696 had an acceptable safety profile and was well tolerated in patients with HF-PEF.
LCZ696 is one of several compounds being developed by Novartis across the spectrum of heart failure. In addition to HF-PEF, LCZ696 is also being investigated for the treatment of heart failure with reduced ejection fraction (HF-REF) in the phase III Paradigm-HF study. A recent phase II study also showed that LCZ696 is more effective than valsartan in reducing blood pressure, and a phase III programme has been launched for the first-line treatment of hypertension in Asia.
Paramount was an international 36-week, randomised, double-blind, multicenter, parallel group, active-controlled study to compare the efficacy, safety, and tolerability profile of LCZ696 with valsartan in patients with HF-PEF. The study consisted of a 12-week core study and a 24-week extension phase. The study included 301 patients (mean age 71 years) with HF-PEF (left ventricular ejection fraction >45 per cent). They all had elevated NT-proBNP (>400 pg/ml) and at least one of the following symptoms of HF-PEF: shortness of breath on exertion, shortness of breath when lying flat, episodes of shortness of breath at night, and swollen ankles. After stopping any treatment with an angiotensin-converting enzyme (ACE) inhibitor or angiotensin receptor blocker (ARB), they were randomised to LCZ696 (50 mg twice-daily) or valsartan (40 mg twice-daily), an ARB indicated for heart failure. Doses of both drugs were doubled after one week and doubled again after a further week to a maximum dose of 200 mg and 160 mg twice-daily, respectively.
EP News Bureau