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Exploratory Study of ADR-002K for Heart Failure Patients with Ischemic Heart Disease who Undergo Coronary Artery Bypass Surgery

Exploratory Study of ADR-002K for Heart Failure Patients with Ischemic Heart Disease who Undergo Coronary Artery Bypass Surgery

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2053250022
Enrollment
50
Registered
2025-05-14
Start date
2025-05-14
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure Patients with Ischemic Heart Disease who Undergo Coronary Artery Bypass Surgery Coronary Artery Bypass Surgery, Ischemic Heart Disease, Adipose-derived Mesenchymal Stem Cells

Interventions

Coronary Artery Bypass Surgery, ADR-002K
D045164

Sponsors

Okawa Sumito
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients who are clinically diagnosed heart failure with ischemic heart disease and receive CABG 2) Patients with a left ventricular ejection fraction of 40% or less before CABG 3) Others

Exclusion criteria

Exclusion criteria: 1) Patients who have a combination of cardiovascular disease such as severe organic valvular disease 2) Patients whose participation in a clinical trial is considered inappropriate at the discretion of the investigator or co-investigator 3) Others

Design outcomes

Primary

MeasureTime frame
Heart Failure Event

Secondary

MeasureTime frame
1) Cardiac Function 2) QOL 3) Others

Contacts

Public ContactToshiyuki Osawa

ROHTO Pharmaceutical Co., Ltd.

R-regenerative_medicine@rohto.co.jp+81-6-6447-8610

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026