Effects of Ranolazine on Coronary Microvascular Dysfunction in Patients With Hypertrophic Cardiomyopathy

PHASE2CompletedINTERVENTIONAL
Enrollment

26

Participants

Timeline

Start Date

October 31, 2016

Primary Completion Date

February 1, 2020

Study Completion Date

March 6, 2020

Conditions
HCM - Hypertrophic Non-Obstructive Cardiomyopathy
Interventions
DRUG

Ranolazine PR (prolonged-release) 500 mg 1 tablet bis in die and 750 mg 1 tablet bis in die

Patients enrolled in the study, at the end of the titration phase will be treated with ranolazine 750 mg or 500 mg, 1 oral tablet twice a day for 4 months on top of standard of care treatment

Trial Locations (1)

20132

IRCCS Ospedale San Raffaele, Milan

All Listed Sponsors
collaborator

Menarini International Operations Luxembourg SA

INDUSTRY

lead

IRCCS San Raffaele

OTHER

NCT03953989 - Effects of Ranolazine on Coronary Microvascular Dysfunction in Patients With Hypertrophic Cardiomyopathy | Biotech Hunter | Biotech Hunter