Efficacy and Safety of AG10 in Subjects With Transthyretin Amyloid Cardiomyopathy
Part of paid clinical trials in Los Angeles, California.
- Sponsor
- Eidos Therapeutics, a BridgeBio company
- Study ID
- NCT03860935
- Phase
- PHASE3
- Status
- Completed
Conditions
- Amyloid Cardiomyopathy
- Amyloidosis
- Cardiomyopathies
- Heart Diseases
- Transthyretin Amyloidosis
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 90 Years
- Healthy Volunteers
- Not accepted
Interventions
- acoramidis — DRUGTTR stabilizer administered orally twice daily (BID)
- Placebo Oral Tablet — DRUGNon-active control administered orally twice daily (BID)
Study Details
Phase 3 efficacy and safety study to evaluate acoramidis (AG10) HCl 800 mg administered orally twice a day compared to placebo in subjects with symptomatic Transthyretin Amyloid Cardiomyopathy (ATTR-CM).
Key Dates
- Start date
- Mar 19, 2019
- Status verified
- Jun 2024
- Primary completion
- May 11, 2023
- Completion
- May 11, 2023
Study Design
- Enrollment
- 632 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: acoramidis HCl 800 mgSubjects will receive acoramidis HCl 800 mg twice daily. 6MWT primary outcome will be assessed at the end of 12 months. The hierarchical combination of All-Cause mortality, cumulative frequency of cardiovascular-related hospitalizations, change from baseline in NT-proBNP levels, and change from baseline in distance walked on the 6MWT will be assessed after 30 months of treatment.
- Placebo Comparator: PlaceboSubjects will receive placebo to match twice daily. 6MWT primary outcome will be assessed at the end of 12 months. The hierarchical combination of All-Cause mortality, cumulative frequency of cardiovascular-related hospitalizations, change from baseline in NT-proBNP levels, and change from baseline in distance walked on the 6MWT will be assessed after 30 months of treatment.
Primary Outcome Measure
A Hierarchical Combination of All-Cause Mortality, Cumulative Frequency of CV-related Hospitalization, Change From Baseline in NT-proBNP and Change From Baseline in 6MWT at the Last Available Visit Where Both Subjects Had Non-missing Assessments. [ Time Frame: Baseline up to Month 30 ]
Locations (40)
Find similar trials in Los Angeles, CA
By research site
Cedars-Sinai Medical Center· Los Angeles, CAPacific Heart Institute· Santa Monica, CAUniversity of Colorado Hospital - Anschutz Medical Campus· Aurora, COYale School of Medicine· New Haven, CTMedStar Washington Hospital Center· Washington D.C., DCUniversity of Miami - Sylvester Comprehensive Cancer Center· Miami, FL
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