Madrid, Spain – 29 August 2025: Digitoxin reduced the risk of a composite of all-cause death and hospitalisation for worsening heart failure (HF) among patients with advanced HF and a reduced ejection fraction (HFrEF), according to a late-breaking trial presented in a Hot Line session today at ESC Congress 2025.1
Explaining the rationale, Principal Investigator, Professor Udo Bavendiek from Hannover Medical School, Germany, said: “Cardiac glycosides, such as digitoxin and digoxin have been used to treat heart failure for two centuries. However, evidence for their beneficial effects in HFrEF comes mainly from a single randomised trial, the DIG trial published in 1997.2 Digoxin had an overall neutral effect on the primary endpoint of mortality in the DIG trial; however, lower serum digoxin levels seemed to be associated with improvements, while higher digoxin levels worsened prognosis. Notably, hospitalisations for worsening HF, a prespecified secondary outcome, were reduced with digoxin and the greatest benefits were seen in patients with pronounced HF symptoms and markedly reduced left ventricular ejection fraction (LVEF). We designed the DIGIT-HF trial with digitoxin – which has stable blood concentrations even in patients with renal dysfunction – and included patients with HF and a pronounced HF symptom burden.”
DIGIT-HF was a double-blind, placebo-controlled randomised trial conducted at 55 sites in Germany, Austria and Serbia. Patients were eligible for inclusion if they had symptomatic HFrEF: NYHA functional class II and a LVEF of ≤30% or NYHA class III–IV and LVEF ≤40%. Patients were randomised 1:1 to digitoxin or placebo on top of standard-care treatment. Patients in the digitoxin group initially received 0.07 mg once daily with double-blind dose adjustment to 0.05 mg or 0.1 mg once daily after 6 weeks to achieve a digitoxin target concentration of 8–18 ng/ml. The primary outcome was a composite of all-cause death and hospital admission for worsening HF (whichever occurred first), analysed according to the intention-to-treat (ITT) principle.
The 1,212 patients in the ITT population had a mean age of 66 years, with 20% being female. The mean LVEF was 29% and the HF symptom burden was high – 70% of patients had NYHA class III or IV. Contemporary pharmacological HF therapy was well implemented across the population, including high uptake of defibrillator-based devices (64%; cardiac resynchronisation therapy 25%).
Over a median of 36 months, the primary outcome occurred in 39.5% of patients in the digitoxin group and 44.1% in the placebo group (hazard ratio [HR] 0.82; 95% confidence interval [CI] 0.69 to 0.98; p=0.03).
In total, 27.2% of patients in the digitoxin group and 29.5% in the placebo group died (HR 0.86; 95% CI 0.69 to 1.07). A first hospital admission for worsening HF occurred in 28.1% of patients in the digitoxin group and 30.4% in the placebo group (HR 0.85; 95% CI 0.69 to 1.05). The total number of deaths from any cause and hospitalisations for worsening HF was 537 in the digitoxin group and 531 in the placebo group (rate ratio 0.85; 95% CI 0.67 to 1.09).
The primary outcome appeared positive in all pre-specified subgroups, but those with heart rate ≥75 bpm or systolic blood pressure ≤120 mmHg appeared to be associated with particular benefit. Regarding safety, serious adverse events occurred in 4.7% of patients in the digitoxin group and 2.8% in the placebo group, predominantly cardiac disorders (3.4% and 1.8%, respectively).
Professor Bavendiek concluded: “We were able to demonstrate that using a simple dose-titration protocol, digitoxin significantly reduced all-cause death and hospitalisation for worsening HF in patients with well-implemented HF therapy, despite lower-than-expected enrolment. Based on our findings, digitoxin represents an additional option for patients with HFrEF, particularly those with atrial fibrillation, higher heart rates, low blood pressure or impaired kidney function.”
ENDS
Notes to editor
Funding: Funding was provided by the Federal Ministry of Education and Research, Germany, the Braukmann-Wittenberg Herzstiftung and the German Heart Foundation.
Disclosures: Professor Bavendiek has received travel support and honoraria for lectures/consulting from Alnylam Pharmaceutical, Amgen, Astra Zeneca, Bayer Vital, Bristol Myers Squibb, Boehringer Ingelheim, Lilly, Novartis, Novo Nordisk and Pfizer and institutional research support from Alnylam Pharmaceuticals, all unrelated to this trial.
References and notes:
1‘DIGIT-HF: Digitoxin in patients with heart failure and reduced ejection fraction’ presented during HOT LINE 1 on 29 August 2025 at 11:30 to 11:40 in Madrid (Main Auditorium).
2Digitalis Investigation Group. The effect of digoxin on mortality and morbidity in patients with heart failure. N Engl J Med. 1997;336:525−533.
ESC Press Office
Tel: +33 661401884
Email: press@escardio.org
The hashtag for ESC Congress 2025 is #ESCCongress
Follow us on LinkedIn @European Society of Cardiology News
Journalists are invited to become accredited and register here.
Check out the ESC Media and Embargo Policy.
It is the world’s largest gathering of cardiovascular professionals, disseminating ground-breaking science both onsite in Madrid and online – from 29 August to 1 September 2025. Explore the scientific programme. More information is available from the ESC Press Office at press@escardio.org.
About the European Society of Cardiology
The ESC brings together healthcare professionals from more than 150 countries, working to advance cardiovascular medicine and help people to live longer, healthier lives.
Journal
New England Journal of Medicine