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NCT06240403
Digoxin and Senolysis in Heart Failure and Diabetes Mellitus
Phase 2 trial testing Digoxin 0.125 MG in Heart Failure, Systolic in 100 participants. Not yet recruiting.
28 August 2028
Quick facts
| Lead sponsor | University of Leeds |
|---|---|
| Phase | Phase 2 |
| Status | Not yet recruiting |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | quadruple |
| Primary purpose | treatment |
| Enrollment | 100 |
| Start date | 1 September 2025 |
| Primary completion | 28 August 2028 |
| Estimated completion | 28 August 2029 |
| Sites | 1 location across United Kingdom |
Drugs / interventions tested
- Digoxin 0.125 MG — full drug profile →
Conditions studied
- Heart Failure, Systolic — all drugs for Heart Failure, Systolic →
- Diabetes Mellitus, Type 2 — all drugs for Diabetes Mellitus, Type 2 →
Sponsor
University of Leeds
Who can join
18 and older, any sex, with Heart Failure, Systolic or Diabetes Mellitus, Type 2. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
In pilot studies the investigators have shown that subcutaneous adipose tissue (SAT) from patients with reduced ejection fraction heart failure (HFrEF) and type 2 diabetes mellitus (T2DM) is dysfunctional. Endothelial cells from the adipose tissue from these patients are senescent and have deleterious effects on healthy human subcutaneous adipocytes, including increasing expression of IL-6 (gene and protein) and reducing glucose uptake. Digoxin, a well-established treatment for HFrEF, selectively clears these senescent endothelial cells and prevents adipocyte dysfunction. This study will examine the effect of digoxin on adipose tissue on the burden of senescent cells.
Publications & conference data
4 peer-reviewed publications reference this trial (live from Europe PMC):
-
Recent Advances in Aging and Immunosenescence: Mechanisms and Therapeutic Strategies.
Wang S, Huo T, Lu M, Zhao Y, et al · · 2025 · cited 20× · PMID 40214453 · DOI 10.3390/cells14070499 -
Anti-senescence therapies: a new concept to address cardiovascular disease.
Stojanović SD, Thum T, Bauersachs J. · · 2025 · cited 9× · PMID 40036821 · DOI 10.1093/cvr/cvaf030 -
The role of cellular senescence in cardiovascular disease.
Xu C, Qiu Z, Guo Q, Huang Y, et al · · 2025 · cited 1× · PMID 41053058 · DOI 10.1038/s41420-025-02720-5 -
Repurposing of NKA inhibitors ('cardiac glycosides'): a critical analysis.
Evans K, Seifert R. · · 2026 · cited 1× · PMID 40679588 · DOI 10.1007/s00210-025-04443-x
Verify or expand the search:
- PubMed search for NCT06240403
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06240403 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by University of Leeds
- Last refreshed: 6 December 2024
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06240403.
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