Build status - In Progress
Studying the Safety and Effectiveness of an Investigation Drug Danicamtiv in Patients with Dilated Cardiomyopathy
Recruiting
18 years - 80 years
All
24 participants needed
1 Location
Brief description of study
The purpose of Part A of this study is to evaluate the safety, tolerability, and cardiac pharmacodynamics (the effect of the study drug on your heart) of the study drug, danicamtiv, when administered by mouth twice a day for approximately one to two weeks.
Part A which may last between 4 and 11 weeks, and an optional Part B which may last up to about 104 weeks.
Detailed description of study
The purpose of Part A of this study is to evaluate the safety, tolerability, and cardiac pharmacodynamics (the effect of the study drug on your heart) of the study drug, danicamtiv, when administered by mouth twice a day for approximately one to two weeks.
Part A which may last between 4 and 11 weeks, and an optional Part B which may last up to about 104 weeks.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: Heart, Dilated Cardiomyopathy
-
Age: 18 years - 80 years
-
Gender: All
Ages 18 to 80 Diagnosed with Dilated Cardiomyopathy (DCM) due to a mutation in either MYH7 or TTN, both of which are genes involved in the function of heart muscle.
Updated on
04 Aug 2024.
Study ID: 848993
Find a site
,
Your Information has been sent successfully.
We have submitted the contact information you provided to the research team at {{SITE_NAME}}. A copy of the message has been sent to your email for your records.
Would you like to be notified about other trials? Sign up for Patient Notification Services.
Sign up
Send a message
Enter your contact details to connect with study team
Primary Contact
Interested in the study
Select a study center that’s convenient for you, and get in touch with the study team.
Contact a study centerPlease choose between Voice or SMS based delivery of verification code
or