This study will evaluate the efficacy and safety of DA-1229 in patients with calcific aortic valve disease.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Enrollment
228
All participants are administered one tablet per day for 96 weeks
Seoul National University Bundang Hospital
Seongnam-si, Bundang-gu, South Korea
Chonnam National University Hospital
Gwangju, Donggu, South Korea
Gangnam Severance Hospital
Seoul, Gangnam-gu, South Korea
aortic valve calcium volume change
aortic valve calcium volume change compared to baseline(mm\^3)
Time frame: 96 weeks
aortic valve calcium volume change
aortic valve calcium volume change compared to baseline(mm\^3)
Time frame: 48 weeks
aortic valve calcium score change
aortic valve calcium score change compared to baseline(AU)
Time frame: 48 weeks, 96 weeks
aortic valve calcium volume change percent
aortic valve calcium volume change percent compared to baseline(%)
Time frame: 48 weeks, 96 weeks
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Samsung Medical Center
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Seoul National University Hospital
Seoul, Jongno-gu, South Korea
Kyeongpook National University Hospital
Daegu, Jung-gu, South Korea
Chungnam National University Hospital
Daejeon, Jung-gu, South Korea
Pusan National University Yangsan Hospital
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Severance
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Asan Medical Center
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