Completed Research Studies | Description |
ASSENT 2 Trial 1998 | Single-bolus tencteplase compared with front-loaded alteplase in acute myocardial infarction. |
LIMIT AMI 1999 | A randomized, controlled, double-blind trial of the safety and efficacy of Anto-CD18 antibody in patients with acute MI. |
ASSENT 3 Trial 2000 | Thrombolytic with heparin, low molecular weight heparin or 2B3A inhibitor. |
Emergent PTCA of Surgical Site 2000 | N/A |
Prospective study of the availability of Lipoprotein subclass results in the process of care, phase 3. 2001 | N/A |
IMPACT 2001 | Study to evaluate the impact of medical subspeciality on patient compliance to treatment. |
CRISP 2001 | Single arm open lable study of Cervistatin. |
RESPOND 2002 | Study to evaluate the efficacy and safety of combination of amlodipine/atorvastatin. |
EASE 2002 | Study to evaluate the safety and efficacy of ezetimibe when added to ongoing therapy with a statin vs stating therapy alone. |
VICTORY 2003 | Study to evaluate the safety and efficacy of ezetimibe/simvastatin combination vs atorvastatin in patients with hypercholesterolemia. |
EZTS44, 2003 | Study to evaluate the safety and efficacy of ezetimibe/simvastatin combination vs atorvastatin with hypercholesterolemia |
ARISE 2003 | Study to evaluate the safety and efficacy for a vascular protectant in patients with acute coronary syndrome. |
MERCK 055, 2004 | Study to evaluate the safety and efficacy of ezetimibe/simvastatin vs rosuvastatin. |
GE Health Care (Amersham) - WOMENS’S STUDY 2004 | A Multi Center, Prospective, Randomized Study to Establish the Optimal Method for Detection of CAD Risk in Women at an Intermediate High Pre-Test Likelihood of CAD. |
RESTORE-US 2004 | Open label study of the effectiveness of CRT in subjects diagnosed with HF-induced conduction disturbances and ventricular dysynchrony. |
CASPER 2005 | Study for controlled assessment of once-daily COREG-CR vs twice daily Coreg immediate release on measures of compliance and quality of life. |
ATHENA 2005 | Study to assess efficacy of dronedarone for the prevention of cardiovascular hospitalization or death from any cause in patients with atrial fibrillation. |
OMNI 2005 | Device data collection to evaluate the effectiveness of pacemaker utilization |
RELY 2006 | Study to evaluate long term anticoagulant therapy comparing dabigatran vs warfarin in subjects with persistent or chronic atrial fibrillation. |
MK653 2007 | Sc-PRAVA-06-02: Pravastatin vs Pravastatin/Fenofibrate Phase 3 study to evaluate the safety and efficacy of daily administration. |
DIONYSOS 2007 | Amiodarone vs Dronedarone randomized double blind trial to evaluate the efficacy and safety for the maintenance of sinus rhythm in patients with atrial fibrillation. |
CRESCENDO 2007 | Metabolic study to reduce risk factor for coronary heart disease patients |
CG107, 2007 | Evaluation of Plavix in conjunction with Proton Pump Inhibitors to identify the decrease in gastrointestinal symptoms. |
Johnson &Johnson - ROCKET 2008 | A Prospective, Randomized, Double-Blind, Double Dummy, Parallel-Group, Multi-Center, Event-Driven, Non-Inferiority Study Comparing the Efficacy and Safety of Once-Daily Oral Rivaroxaban (BAY 59-7939) with Adjusted-Dose Oral Warfarin for the Prevention of Stroke and Non-Central Nervous System Systemic Embolism in Subjects with Non-Valvular Atrial Fibrillation. |
CV-Therapeutics – CVT 3041, 2008 | An Open-Label, Mulit-Center Study Evaluating the Validity, Reliability, and Responsiveness of a New Women’s Ischemia Symptom Questionnaire in Women with Chronic Angina Treated with Ranolazine Extended-Release Tablets |
Roche CV M&M – NC20971 RG 2008 | : Roche Sample Respository Research Project in conjunction with protocol NC20971. A phase 3, double-blind, randomized placebo-controlled study, to evaluate the effects of RO4607381 on cardiovascular (CV) risk in stable CHD patients, with a documented recent Acute Coronary Syndrome (ACS) |
Daiichi Sankyo ENGAGE – DU176b-C-U301, 2008 | A Phase 3, Randomized, Double-blind, Double-Dummy, Parallel Group, Mulit-Center, Multi-National Study for Evaluation of Efficacy and Safety of DU-176B vs. Warfarin in Subjects with Atrial Fibrillation – Effective aNticoaGulation with factor xA next Generation in Atrial Fibrillation (ENGAGE AF – TIMI48). |
Johnson & Johnson Atlas RIVAROX ACS 3001, 2008 | A Randomized, Double-Blind, Placebo-Controlled, Event-Driven Multicenter Study to Evaluate the Efficacy and Safety of Rivaroxaban in Subjects With a Recent Acute Coronary Syndrome. |
Integrium Resverlogix 2010 | A Phase II, Multi-Center, Double-Blind, Randomized, Parallel Group, Placebo-Controlled Clinical Trial For Dose-Finding And Safety Study Of RVX000222 In Subjects With Stable Coronary Artery Disease. |
Bristol Myers Squibb, Pfizer Inc. CV185068 APPRISE-2, 2010 | A Phase 3, Randomized, Double Blind, Evaluation of the Safety and Efficacy of Apixaban in Subjects with a Recent Acute Coronary Syndrome |
NovartisCLCZ696B2314, 2010 | A multicenter, randomized, double-blind, parallel group, active-controlled study to evaluate the efficacy and safety of LCZ696B compared to enalapril on morbidity and mortality in patients with chronic heart failure and reduced ejection fraction. |