Determine Edwards Lifesciences Corp go-to-market proposition and gain insight into the company’s clinical operations, recruitment, and trial strategy.
|Trial Title||Trial Identifier||Drug Name||Therapy Area||Indication||Trial Phase||Trial Status||Sponsor|
|Deserunt mollit sunt Lorem||GDCTXXXX||Lorem||Lorem||Lorem||XXXX||Planned||Pfizer Inc|
|Treatment of Lower Extremity Critical Limb Ischemia via Modulation of VEGF-A Using an Engineered Zinc-finger Transcription Factor (EW-A-401) to Evaluate Safety and the Effects on Progenitor Cells||GDCT0193418||EW-A-401||Cardiovascular||Coronary Artery Disease (CAD) (Ischemic Heart Disease); Critical Limb Ischemia; Intermittent Claudication; Peripheral Arterial Disease (PAD)/ Peripheral Vascular Disease (PVD)||Phase I||Completed||Edwards Lifesciences Corp|
|Aspirin Versus Aspirin Plus Clopidogrel Following Transcatheter Aortic Valve Implantation: The ARTE Trial||GDCT0150291||aspirin; clopidogrel bisulfate||Cardiovascular||Aortic Valve Diseases; Ischemic Stroke; Myocardial Infarction||Phase IV||Completed||University Institute of Cardiology and Pneumology of Quebec|
|Efficacy Assessment of Repeat Intramyocardial Injection of Autologous Bone Marrow Cells in Previously Responding No-option Patients with Residual or Recurrent Refractory Angina Pectoris and Documented Ischemia||GDCT0138027||autologous bone marrow derived mononuclear cells||Cardiovascular||Angina (Angina Pectoris); Coronary Artery Disease (CAD) (Ischemic Heart Disease); Myocardial Ischemia||Phase III||Completed||Leiden University Medical Center|
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