You’re using a public version of DrugPatentWatch with 5 free searches available | Register to unlock more free searches. CREATE FREE ACCOUNT

Last Updated: May 29, 2024

CLINICAL TRIALS PROFILE FOR RANEXA


✉ Email this page to a colleague

« Back to Dashboard


All Clinical Trials for Ranexa

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00099788 ↗ Metabolic Efficiency With Ranolazine for Less Ischemia in Non-ST Elevation Acute Coronary Syndromes Completed The TIMI Study Group Phase 3 2004-10-01 MERLIN-TIMI 36 is a multi-national, double-blind, randomized, placebo-controlled, parallel-group clinical trial designed to evaluate the efficacy and safety of ranolazine during acute and long-term treatment in approximately 5,500 patients with non-ST elevation acute coronary syndromes (ACS) treated with standard therapy. The primary efficacy endpoint in MERLIN-TIMI 36 is time to first occurrence of any element of the composite of cardiovascular death, myocardial infarction or recurrent ischemia in patients with non-ST elevation ACS receiving standard therapy. The study also evaluates the safety of long-term treatment with ranolazine compared to placebo.
NCT00099788 ↗ Metabolic Efficiency With Ranolazine for Less Ischemia in Non-ST Elevation Acute Coronary Syndromes Completed Gilead Sciences Phase 3 2004-10-01 MERLIN-TIMI 36 is a multi-national, double-blind, randomized, placebo-controlled, parallel-group clinical trial designed to evaluate the efficacy and safety of ranolazine during acute and long-term treatment in approximately 5,500 patients with non-ST elevation acute coronary syndromes (ACS) treated with standard therapy. The primary efficacy endpoint in MERLIN-TIMI 36 is time to first occurrence of any element of the composite of cardiovascular death, myocardial infarction or recurrent ischemia in patients with non-ST elevation ACS receiving standard therapy. The study also evaluates the safety of long-term treatment with ranolazine compared to placebo.
NCT00570089 ↗ Microvascular Coronary Disease In Women: Impact Of Ranolazine Completed CV Therapeutics Phase 2 2007-04-01 1. To evaluate the impact of ranolazine extended-release tablets in women with subendocardial ischemia due to microvascular endothelial dysfunction on myocardial ischemia (Cardiac Magnetic Resonance (CMR) extent, severity. 2. To evaluate the impact of ranolazine extended-release tablets in women with subendocardial ischemia due to microvascular endothelial dysfunction on the outcomes of angina (Seattle Angina Questionnaire (SAQ), WISE angina frequency, Duke Activity Status Inventory(DASI) and SF-36).
NCT00570089 ↗ Microvascular Coronary Disease In Women: Impact Of Ranolazine Completed Cedars-Sinai Medical Center Phase 2 2007-04-01 1. To evaluate the impact of ranolazine extended-release tablets in women with subendocardial ischemia due to microvascular endothelial dysfunction on myocardial ischemia (Cardiac Magnetic Resonance (CMR) extent, severity. 2. To evaluate the impact of ranolazine extended-release tablets in women with subendocardial ischemia due to microvascular endothelial dysfunction on the outcomes of angina (Seattle Angina Questionnaire (SAQ), WISE angina frequency, Duke Activity Status Inventory(DASI) and SF-36).
NCT00574756 ↗ Effect of Ranolazine on Echocardiographic Indices of Diastolic Dysfunction Terminated University of California, San Diego N/A 2007-12-01 The purpose of this study is to evaluate the effects of ranolazine, an FDA-approved medication for the treatment of angina, on heart function by using echocardiography.
NCT00832572 ↗ Study of Ranexa in Patients With Coronary Artery Disease and Painful Polyneuropathy Terminated Gilead Sciences Phase 4 2009-01-01 This study was to determine whether ranolazine was effective in the treatment of neuropathic pain in patients with coronary artery disease. Eligibility required neurological examination by the study doctor and assessment of the patient's pain. Eligible participants were randomized to receive blinded study medication for a total of 12 weeks.
NCT00914316 ↗ Supervised Treadmill Exercise and Ranolazine for Intermittent Claudication of Lower Extremities Terminated William Beaumont Hospitals N/A 2009-05-01 The goal of this study is to evaluate whether supervised treadmill exercise combined with ranolazine 1000 mg twice daily provides an incremental benefit in absolute walking distance over supervised exercise alone in patients with stable claudication. Investigators also seek to determine if the administration of ranolazine provides a sustained benefit after the completion of a supervised exercise regimen. Lastly, investigators wish to determine whether both exercise and ranolazine improves peak oxygen consumption and anaerobic threshold in patients with stable claudication.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Ranexa

Condition Name

Condition Name for Ranexa
Intervention Trials
Coronary Artery Disease 8
Angina 6
Myocardial Ischemia 3
Type 2 Diabetes Mellitus 3
[disabled in preview] 0
This preview shows a limited data set
Subscribe for full access, or try a Trial

Condition MeSH

Condition MeSH for Ranexa
Intervention Trials
Coronary Artery Disease 15
Myocardial Ischemia 15
Coronary Disease 11
Ischemia 8
[disabled in preview] 0
This preview shows a limited data set
Subscribe for full access, or try a Trial

Clinical Trial Locations for Ranexa

Trials by Country

Trials by Country for Ranexa
Location Trials
United States 107
Poland 8
Canada 8
Germany 7
France 5
This preview shows a limited data set
Subscribe for full access, or try a Trial

Trials by US State

Trials by US State for Ranexa
Location Trials
Florida 8
Massachusetts 7
California 7
Louisiana 5
Maryland 5
This preview shows a limited data set
Subscribe for full access, or try a Trial

Clinical Trial Progress for Ranexa

Clinical Trial Phase

Clinical Trial Phase for Ranexa
Clinical Trial Phase Trials
Phase 4 16
Phase 3 7
Phase 2/Phase 3 1
[disabled in preview] 21
This preview shows a limited data set
Subscribe for full access, or try a Trial

Clinical Trial Status

Clinical Trial Status for Ranexa
Clinical Trial Phase Trials
Completed 27
Terminated 9
Unknown status 8
[disabled in preview] 2
This preview shows a limited data set
Subscribe for full access, or try a Trial

Clinical Trial Sponsors for Ranexa

Sponsor Name

Sponsor Name for Ranexa
Sponsor Trials
Gilead Sciences 29
University of Florida 3
Brigham and Women's Hospital 3
[disabled in preview] 8
This preview shows a limited data set
Subscribe for full access, or try a Trial

Sponsor Type

Sponsor Type for Ranexa
Sponsor Trials
Other 52
Industry 31
U.S. Fed 1
[disabled in preview] 0
This preview shows a limited data set
Subscribe for full access, or try a Trial

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.