Efficacy, Safety, and PopPK Profile of ABP-745 in Patients With Atherosclerosis

Recruiting Phase 2 Interventional Study
Atherosclerosis Cardiovascular Disease ASCVD ASCVD Management
Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 – 75
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
200 (estimated)
Sponsor
Atom Therapeutics Co., Ltd · Industry
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About This Trial

This is a multicenter, randomized, double-blind, placebo parallel controlled study to evaluate the preliminary efficacy, safety, and PopPK profile of ABP-745 in patients with ASCVD. Efficacy of ABP-745 in reducing atherosclerotic plaque compared with placebo will be evaluated in participants with ASCVD. The primary efficacy measurement will be assessed at 52W of treatment.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: Unless otherwise specified, subjects must meet all of the following criteria at screening: * Diagnosed with coronary at herosclerosis, and coronary angiography. * Male or female at 18-75 years of age (inclusive). * Weight ≥40 kg. * Currently using any oral lipid-lowering therap…
Contacts

Qiang Shi

86+ 19117302212

qiang.shi@atombp.com

CONTACT