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A Phase 2, Double-Blind, Randomized, Placebo-Controlled Study To Evaluate The Effect Of RBT-1 On Preconditioning Response Biomarkers In Subjects Undergoing Coronary Artery Bypass Graft (CABG) And/or Cardiac Valve Surgery
(START)
Rochester, Minn.
The purpose of this study is to evaluate the effect of RBT-1 on preconditioning response biomarkers in subjects who are at risk for acute kidney injury (AKI) following cardiac surgery.
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A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study To Evaluate The Effect Of RBT-1 On Reducing The Risk Of Post-Operative Complications In Subjects Undergoing Cardiac Surgery And Sub-Study Of Clinical Protocol REN-007: A Population Pharmacokinetic (PopPK) Evaluation Of RBT-1
Rochester, Minn.
The purpose of this study is is to evaluate the effect of RBT-1 on reducing the risk of post-operative complications in subjects undergoing cardiac surgery on cardiopulmonary bypass (CPB).
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A Phase II, Randomized, Double-Blind, Placebo-Controlled Study Of The Efficacy And Safety Of GDC-8264 In Preventing Cardiac Surgery-Associated Acute Kidney Injury And Major Adverse Kidney Events
Rochester, Minn.
The purpose of this study is to evaluate the efficacy and safety of GDC-8264 compared with placebo in participants undergoing cardiac surgery who are determined to be at moderate to high risk of developing AKI and subsequent MAKE at 90 days after surgery (MAKE90).
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A Prospective, Multi-center Trial To Evaluate The Safety And Effectiveness Of Beating Heart Mitral Valve Repair With The HARPOON™System (RESTORE), Protocol 2019-05
Rochester, Minn.
The purpose of this study is to evaluate the safety and effectiveness of the HARPOON System in the treatment of patients with severe degenerative mitral regurgitation.
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Hybrid Convergent of Epicardial and Endocardial RF Ablation for the Treatment of Symptomatic Longstanding Persistent AF
Rochester, Minn.
The primary objective of CONVERGE PAS is to evaluate clinical outcomes (peri-procedural and long-term) in a cohort of patients treated during commercial use of the EPi-Sense® Guided Coagulation System or EPi-Sense ST™ Coagulation System to treat symptomatic long-standing persistent atrial fibrillation (AF) patients who are refractory or intolerant to at least one Class I and/or III AAD.
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