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A Study of SRSD107 in Participants With Chronic Coronary and/or Peripheral Arterial Disease
RECRUITINGPhase 2Sponsored by Sirius Therapeutics Co., Ltd.
Actively Recruiting
PhasePhase 2
SponsorSirius Therapeutics Co., Ltd.
Started2025-03-11
Est. completion2027-12
Eligibility
Age18 Years – 75 Years
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT07318155
Summary
The study is a Phase 2a, randomized, double-blind, placebo-controlled, sequential cohort study to evaluate the pharmacodynamics (PD), safety and pharmacokinetics (PK) of multiple doses of SRSD107 in participants with coronary arterial disease (CAD) and/or peripheral arterial disease (PAD) with aspirin as background concomitant therapy.
Eligibility
Age: 18 Years – 75 YearsHealthy volunteers accepted
Inclusion Criteria: * Able to comprehend and willing to sign an ICF and to abide by the study restrictions. * Males or females aged 18 to 75 years, inclusive. * Body mass index (BMI) between 18.0 and 35.0 kg/m2, inclusive. * History of chronic coronary and/or peripheral arterial disease Exclusion Criteria: * Known bleeding disorder * Severe heart failure with known left ventricular ejection fraction \<35%, or New York Heart Association (NYHA) class III or IV symptoms. * Genetic cardiomyopathies or other non-ischemic cardiomyopathies that are not related to atherosclerotic cardiovascular disease. * History of ethanol abuse or addictive drug use (cannabis products allowed) within 6 months of screening. * Receipt of an investigational drug (IP) within 30 days or 5 half-lives of that drug, whichever is longer, prior to dose administration in this study. * Previous use of SRSD107.
Conditions3
Coronary Artery Disease (CAD)Heart DiseasePeripheral Arterial Disease
Interventions2
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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.
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Actively Recruiting
PhasePhase 2
SponsorSirius Therapeutics Co., Ltd.
Started2025-03-11
Est. completion2027-12
Eligibility
Age18 Years – 75 Years
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT07318155