Denna sida har översatts automatiskt och översättningens korrekthet kan inte garanteras. Vänligen se engelsk version för en källtext.

Single Ascending Dose Study of ATH-097 in Healthy Participants

8 juni 2026 uppdaterad av: Atheron Therapeutics, Ltd.

A Randomized, Double-Blind, Placebo-Controlled, Single Ascending Dose Study to Evaluate the Safety, Tolerability and Pharmacokinetics of ATH-097 in Healthy Participants

This is a Phase I, A Randomized, Double-Blind, Placebo-Controlled, Single Ascending Dose Study to Evaluate the Safety, Tolerability and Pharmacokinetics of ATH-097 in Healthy Participants

Studieöversikt

Status

Har inte rekryterat ännu

Studietyp

Interventionell

Inskrivning (Beräknad)

44

Fas

  • Fas 1

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

Studieorter

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Vuxen

Tar emot friska volontärer

Ja

Beskrivning

Inclusion Criteria:

  1. Participants must be able and willing to provide informed consent.
  2. Participants must be aged 18 to 55 years at the time of consent.
  3. Participants must have a BMI within the range 18.5 to 29.9 kg/m2.
  4. Participants must be in general good health.
  5. All female participants of childbearing potential and all male participants who are able to father children and are sexually active and whose partners are at risk for pregnancy, must agree to use a highly effective method of contraception in combination with a condom from the time of signing the informed consent form through 94 days after the last IP administration.

Exclusion Criteria:

  1. Have any condition that, in the investigator's opinion, might jeopardize the participant's safety or compliance with the protocol.
  2. Have a history of any severe allergic reaction or anaphylaxis.
  3. Have clinically significant abnormalities in clinical laboratory results, as judged by the Investigator, including estimated glomerular filtration rate (eGFR) < 90 mL/min/1.73 m² (CKD-EPI 2021 formula).
  4. Have participated in another interventional clinical trial and received an investigational drug within 28 days (or as determined by local requirements) or 5 half-lives prior to Day 1, whichever is longer, or are currently participating in another interventional clinical trial.
  5. Have experienced major trauma or undergone major surgery within 3 months prior to Day 1.
  6. Have a history of malignancy within 5 years before the screening visit, except for curatively treated carcinoma in situ of the cervix or non-metastatic squamous or basal cell carcinoma of the skin.
  7. Have screening seated blood pressure ≥ 140 mm Hg (systolic) or ≥ 90 mm Hg (diastolic).
  8. Have a screening 12-lead ECG with clinically relevant abnormalities that may affect the participant's safety or the interpretation of study results.
  9. Have any of the following active or recent infections:

    1. serious infection requiring hospitalization or parenteral antibiotics within 12 weeks prior to Day 1, serious bone/joint infection within 24 weeks, or history of infection of an artificial joint;
    2. active herpes simplex or herpes zoster outbreak within 12 weeks prior to Day 1;
    3. active infection requiring systemic antimicrobial treatment within 4 weeks prior to Day 1, or superficial skin infection requiring antibiotics within 1 week prior to Day 1;
    4. active TB; or (e) immunocompromised status posing unacceptable risk per investigator judgment.
  10. Have chronic hepatitis B, defined as positive hepatitis B surface antigen (HBsAg) or detectable hepatitis B virus (HBV) DNA at screening. Note: Participants who are hepatitis B core antibody (HBcAb) positive and HBV DNA undetectable may be eligible.
  11. Have hepatitis C infection, defined as positive hepatitis C antibody (HCV Ab) with detectable HCV RNA. Participants with a history of hepatitis C treatment with undetectable HCV RNA at least 24 weeks after completion of treatment may be eligible.
  12. Have a history of human immunodeficiency virus (HIV) infection or be positive for HIV at screening.
  13. Have active or untreated syphilis infection, defined as a reactive Toluidine Red Unheated Serum Test (TRUST) or Treponema pallidum antibody (TP Ab) positive at screening.
  14. Have known or suspected intolerance or hypersensitivity to any components of the formulation of ATH-097 and its excipients.
  15. Have a history of drug abuse or addiction within 6 months of screening.
  16. Have consumed more than 14 units of alcohol per week on average within 3 months prior to Day 1, or be unwilling to abstain completely from alcohol consumption from 7 days prior to Day 1 through discharge.
  17. Be a current smoker defined as smoking more than 5 cigarettes (or equivalent nicotine-containing products) per week within the 6 months prior to Day 1, or have a positive urine cotinine test at Screening or Day -1.
  18. Consume more than 5 cups of coffee, tea, or other caffeine-containing beverages per day on average within 3 months prior to Day 1, or be unwilling to abstain from all caffeine-containing products from 48 hours prior to Day 1 through discharge.
  19. Have received live or attenuated vaccine(s) within 12 weeks prior to screening or plan to receive such vaccines during the study.
  20. Have received biologic immunomodulatory agents within 3 months or 5 half-lives (whichever is longer) prior to dosing.
  21. Have donated blood (excluding plasma donations) of approximately 1 pint (500 mL) or more within 30 days prior to Screening.
  22. Have received a transfusion of blood or blood products within 30 days prior to Day 1 dosing.
  23. If female, be nursing, lactating, pregnant, or planning to become pregnant within 94 days after the last dose of IP.
  24. Have used any prescription or over-the-counter (OTC) medications, herbal preparations, dietary supplements, or vitamins that may affect the metabolism or pharmacokinetics of ATH-097 within 14 days or 5 half-lives (whichever is longer) prior to Day 1.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Fyrdubbla

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Placebo-jämförare: Placebo
Oral Suspension: Dosing volume identical to the experimental arm
Experimentell: ATH-097
Oral Suspension, 6 dose levels

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
The number and severity of treatment emergent adverse events (TEAEs)
Tidsram: 8 days after single dose
The incidence, severity, and relationship to IP of AEs. Change from Baseline in clinical laboratory parameters, physical examination findings, vital signs, and 12-lead ECG
8 days after single dose

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
To evaluate the pharmacokinetics (PK) of a single dose of ATH-097 in healthy participants.
Tidsram: Up to 96 hours post dose.
Peak plasma Concentration (Cmax)
Up to 96 hours post dose.
To evaluate the pharmacokinetics (PK) of a single dose of ATH-097 in healthy participants.
Tidsram: Up to 96 hours post dose
Area under the drug concentration-time curve (AUC)
Up to 96 hours post dose
To evaluate the pharmacokinetics (PK) of a single dose of ATH-097 in healthy participants.
Tidsram: Up to 96 hours post dose
Apparent terminal half-life (t½)
Up to 96 hours post dose

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Beräknad)

6 juli 2026

Primärt slutförande (Beräknad)

20 oktober 2026

Avslutad studie (Beräknad)

20 oktober 2026

Studieregistreringsdatum

Först inskickad

4 juni 2026

Först inskickad som uppfyllde QC-kriterierna

8 juni 2026

Första postat (Faktisk)

10 juni 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

10 juni 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

8 juni 2026

Senast verifierad

1 juni 2026

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • ATH-097-101

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Nej

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

Prenumerera