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Study identifier: NCT07303777 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

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

Condition: Atherosclerosis Cardiovascular Disease · ASCVD · ASCVD Management  ·  Sponsor: Atom Therapeutics Co., Ltd

PhasePhase 2
Planned participants200
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Qiang Shi  ·  86+ 19117302212  ·  qiang.shi@atombp.com

Always discuss trial participation with your own doctor first.

Locations (33)

Cardiovascular Research Foundation of Southern CaliforniaBeverly Hills, California, United StatesNot Yet Recruiting
Cardiovascular Institute of San Diego INCSan Diego, California, United StatesNot Yet Recruiting
The Lundquist InstituteTorrance, California, United StatesNot Yet Recruiting
Washington University School of Medicine, St.louisSt Louis, Missouri, United StatesNot Yet Recruiting
NovaTrailsNewcastle, New South Wales, AustraliaNot Yet Recruiting
University of the Sunshine Coast Clinical Trials Unit - MorayfieldMorayfield, Queensland, AustraliaNot Yet Recruiting
Core Research Group Pty LtdBrisbane, AustraliaNot Yet Recruiting
UniSC Clinical Trials (Brisbane)Brisbane, AustraliaNot Yet Recruiting
CognivusWahroonga, AustraliaNot Yet Recruiting
Beijing Friendship Hospital, Capital Medical UniversityBeijing, ChinaNot Yet Recruiting
Peking Union Medical College HospitalBeijing, ChinaNot Yet Recruiting
Peking University First HospitalBeijing, ChinaNot Yet Recruiting

+ 21 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07303777