NCT07215923 A First in Human Single Ascending Dose (SAD) Study of ATI-1013 in Healthy Smokers

Eligibility & Interventions

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

Phase 1 is the earliest stage of human testing — safety and dosage are the primary focus. Visits are frequent and medical supervision is intensive. You will be among the first people to receive this treatment.

This trial targets 15 participants in total. It began in 2025-10 with a primary completion date of 2026-06-30.

Brief Summary

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.

Eligibility Criteria

Inclusion Criteria 1. Provides written informed consent before any study procedures 2. Age 23 to 59 years, inclusive 3. Body weight ≥50 kg at Screening 4. Body mass index (BMI) 18.5-29.9 kg/m² at Screening 5. In good health with no medically significant conditions, in the opinion of the Investigator 6. Current smoker, ≥10 cigarettes per day for ≥2 years, with no abstinence \>6 months 7. Female participants must agree not to donate ova during the study and for 90 days after dosing 8. Female participants of childbearing potential must use an acceptable, effective method of birth control from 30 days prior to Screening through 90 days after dosing 9. Female participants of non-childbearing potential must be surgically sterile (hysterectomy, bilateral salpingectomy, bilateral oophorectomy, or tubal ligation) or postmenopausal (≥1 year without menses) 10. Male participants must agree to use contraception and not donate sperm for 90 days after dosing 11. Willing to abstain from all other tobacco products from Day -2 through Day 84 12. Willing to abstain from all other nicotine products from Day -2 through Day 84 13. Willing to abstain from smoking regular cigarettes: 1. Approximately 18 hours from evening of Day -2 2. Approximately 42 hours from evening of Day -1 Exclusion Criteria 1. Pregnant, breastfeeding, or planning pregnancy 2. Positive serum pregnancy test at Screening or urine pregnancy test on Day -2 (women only) 3. Prior exposure to any anti-nicotine vaccine or antibody 4. Use of mentholated tobacco products within 30 days before Screening, unwilling to refrain during the study 5. History of severe allergic reaction to antibodies or vaccines (including Guillain-Barré syndrome) 6. Received any vaccination within 90 days prior to Screening 7. Clinically significant allergic adverse reaction (seasonal allergies allowed) 8. Use of systemic steroids or immunomodulating drugs within 90 days (inhaled steroids allowed) 9. History of cancer (except treated basal/squamous cell skin cancer), HIV, other immunodeficiency, or autoimmune disease 10. History of drug (excluding nicotine) or alcohol use disorder (DSM-5 criteria) 11. Clinically significant cardiovascular, respiratory, hepatic, renal, gastrointestinal, endocrine, neurological, or psychiatric disorder, as determined by the Investigator 12. Clinically significant abnormal clinical chemistry, hematology, or urinalysis at Screening or Day -2, in the opinion of the Investigator 13. COVID-19 within the past 6 months or ongoing symptoms likely attributable to COVID-19 14. Use of varenicline, bupropion, nicotine replacement therapy (NRT), or other anti-smoking pharmacologic treatments (including off-label nortriptyline, clonidine, or cytisinicline) within 90 days prior to Screening 15. Received an investigational product within 30 days (90 days for biologics) or 5 half-lives (whichever is longer) prior to Screening 16. Exhaled carbon monoxide (CO) \<8 ppm at Screening 17. Positive test for hepatitis B surface antigen, hepatitis C antibody, or HIV antibody at Screening 18. Positive urine alcohol test at Screening and/or Day -2 19. Positive urine drug test (e.g., cocaine, amphetamines, barbiturates, opiates, benzodiazepines, cannabinoids) at Screening and/or Day -2 20. Unwilling to abstain from xanthine-containing products (coffee, tea, cola, chocolate, energy drinks) within 24 hours prior to admission until discharge 21. Unwilling to abstain from alcohol or alcohol-containing products within 24 hours prior to admission until discharge 22. Significant blood donation or blood loss \>500 mL within 56 days before Screening 23. Plasma donation or loss within 30 days prior to Screening through Day 84 24. Hypersensitivity to the study drug, its excipients, or similar products 25. Unable or unwilling to comply with protocol requirements, restrictions, or instructions 26. Currently enrolled in another clinical study

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