RECRUITINGOBSERVATIONAL
Mavacamten Post-marketing Surveillance in Patients With Obstructive Hypertrophic Cardiomyopathy in Japan
Mavacamten Post-marketing Surveillance in Patients With Obstructive Hypertrophic Cardiomyopathy (oHCM) in Japan
About This Trial
The purpose of this study is to assess the real-world effectiveness and safety of mavacamten in patients with obstructive hypertrophic cardiomyopathy (HCM) receiving mavacamten in Japan
Who May Be Eligible (Plain English)
Who May Qualify:
• All obstructive hypertrophic cardiomyopathy (oHCM) patients who initiate treatment with Mavacamten of the approved indications at medical institutions in Japan during enrollment period will be enrolled in this regulatory post-marketing surveillance (PMS) study
Who Should NOT Join This Trial:
• Participants receiving Mavacamten for an off-label indication will be excluded from this PMS study
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
Inclusion Criteria:
• All obstructive hypertrophic cardiomyopathy (oHCM) patients who initiate treatment with Mavacamten of the approved indications at medical institutions in Japan during enrollment period will be enrolled in this regulatory post-marketing surveillance (PMS) study
Exclusion Criteria:
• Participants receiving Mavacamten for an off-label indication will be excluded from this PMS study
Treatments Being Tested
DRUG
Mavacamten
According to the product label
Locations (1)
CMIC Co., Ltd
Tokyo, Japan