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Study identifier: NCT07215923 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A First in Human Single Ascending Dose (SAD) Study of ATI-1013 in Healthy Smokers

Condition: Thromboangiitis Obliterans (Buerger's Disease)  ·  Sponsor: Antidote Therapeutics, Inc

PhasePhase 1
Planned participants15
Who can joinAll sexes, 23 Years to 59 Years
Healthy volunteersYes

About this study

This study is a first-in-human clinical trial of drug ATI-1013, in healthy adult cigarette smokers. The main questions it aims to answer are to learn about the safety of drug ATI-1013, how long drug ATI-1013 remains within the body, does drug ATI-1013 trigger an immune response, and the effects of drug ATI-1013 on nicotine levels within the body. The clinical trial will compare drug ATI-1013 to a placebo (a look-alike substance that contains no drug) to see if drug ATI-1013 has comparable safety. Participants will have a Screening visit (Day -28 to -3) and will be admitted on Day -2. Each participant will receive one intravenous (IV) infusion of ATI-1013 or placebo (Day 1). Participants will remain in-clinic for at least 48 hours post-dose and return for follow-up visits on Days 7, 21, 42, 56, and 84, with telephone check-ins on Days 5, 14, 28, and 70. Participants will keep a diary of their cigarette use and smoking behaviors.

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

Talk to the study team

Leslie OToole  ·  412-352-3504  ·  lotoole@antidotetx.com

Arjen DeVos, MD  ·  443-994-3244

Always discuss trial participation with your own doctor first.

Locations (1)

Dr. Vince Clinical ResearchOverland Park, Kansas, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07215923