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NCT05507879
TRPC6 Characterization to Predict and Prevent Chemotherapy Related Cardiomyopathy and Heart Failure With Breast Cancer
trial testing Biospecimen Collection in Breast Carcinoma in 200 participants. Currently enrolling.
1 September 2026
Quick facts
| Lead sponsor | Mayo Clinic |
|---|---|
| Status | Recruiting now |
| Study type | OBSERVATIONAL |
| Enrollment | 200 |
| Start date | 26 September 2022 |
| Primary completion | 1 September 2026 |
| Estimated completion | 1 September 2027 |
| Sites | 2 locations across United States |
Drugs / interventions tested
- Biospecimen Collection — full drug profile →
- Electronic Medical Record
Conditions studied
- Breast Carcinoma — all drugs for Breast Carcinoma →
- Cardiomyopathy — all drugs for Cardiomyopathy →
- Congestive Heart Failure — all drugs for Congestive Heart Failure →
Sponsor
Mayo Clinic
Who can join
18 and older, any sex, with Breast Carcinoma or Cardiomyopathy. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This study examines TRPC6 in predicting and preventing chemotherapy related cardiac toxicity and heart failure in patients with breast cancer. Cardiac toxicity, changes in heart function is a well-recognized complication of certain cancer related therapies. Understanding these changes may allow early intervention against therapy-related cardiac toxicity and also identify novel therapeutic targets to protect patient long-term cardiac health. Studying samples of blood from patients with breast cancer in the laboratory may help doctors learn more about changes that occur in deoxyribonucleic acid (DNA), identify biomarkers related to cardiac toxicity, and prevent the development of therapy-induced cardiac toxicity in patients receiving chemotherapy.
Publications & conference data
4 peer-reviewed publications reference this trial (live from Europe PMC):
-
TRP Channels in Cancer: Signaling Mechanisms and Translational Approaches.
Marini M, Titiz M, Souza Monteiro de Araújo D, Geppetti P, et al · · 2023 · cited 39× · PMID 37892239 · DOI 10.3390/biom13101557 -
Navigating cancer therapy induced cardiotoxicity: From pathophysiology to treatment innovations.
Tetterton-Kellner J, Jensen BC, Nguyen J. · · 2024 · cited 20× · PMID 38901637 · DOI 10.1016/j.addr.2024.115361 -
TRP channels and cancer modulation: a voyage beyond metabolic reprogramming, oxidative stress and the advent of nanotechnologies in targeted therapy.
Giannaccari M, Florindi C, Bloise N, Moccia F, et al · · 2025 · cited 9× · PMID 40813985 · DOI 10.1186/s13046-025-03495-4 -
Physiological functions and pharmacological targeting of transient receptor potential channels.
Chubanov V, Grimm C, Hill K, Schaefer M, et al · · 2025 · PMID 41118703 · DOI 10.1016/j.pharmr.2025.100089
Verify or expand the search:
- PubMed search for NCT05507879
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Mayo Clinic trials
Trials by the same sponsor.
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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 NCT05507879 (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 Mayo Clinic
- Last refreshed: 10 February 2026
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/NCT05507879.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing