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

The Safety and Pharmacokinetics Study of TAKC-02 Inhalation Solution in Healthy Adult Males.

30 maj 2022 uppdaterad av: TAK-Circulator Co.

MEX3B is an RNA-binding protein that is conserved in many animal species and has wide range of biological function. The MEX3B protein is deeply involved in the expression of various cytokines associated with the onset and exacerbation of several diseases such as inflammatory diseases, metabolic diseases, and malignant tumors. TAKC-02 is a nucleic acid medicine, antisense oligonucleotide, inhibits the MEX3B synthesis expected to have potential as new medication.

This plans to evaluate the safety profile of the inhalation solution in order to develop TAKC-02 for severe asthma.

The study is a double-blind, randomized, placebo-controlled Phase I study. The primary objective of the study is to assess the safety and tolerability of single and multiple inhaled doses of TAKC-02 in healthy male subjects. The study is a Single Ascending Dose (Step 1) followed by a Multiple Comparative Dose (Step 2).

Studieöversikt

Status

Avslutad

Betingelser

Detaljerad beskrivning

This initial Phase I study will be conducted in normal healthy male volunteers to obtain an unconfounded understanding of the safety, tolerability and pharmacokinetics of TAKC-02 inhalation solution. TAKC-02 is being developed as a medication for uncontrolled severe asthma. The first-in-human, randomized, double-blind trial will evaluate single ascending doses (SAD) and subsequently multiple ascending doses (MAD) of TAKC-02 and placebo.

Step 1 (SAD) :

There will be 5 cohort of 6 (Cohort 1, 2, 3) or 8 (Cohort 4, 5) subjects each. Subjects in each cohort are randomized in a 2:1 ratio (Cohort 1, 2, 3) and 3:1 ratio to receive a single dose of the study drugs, TAKC-02 or Placebo. The SAD study will evaluate the safety and tolerability of a single dose of TAKC-02 and determine the starting and maximum doses for Step 2. Pharmacokinetics will be also analyzed. One cohort (cohort 4.5) maybe added depending on the incidence of adverse effect in the lower dosing group.

Step 2 There will be 2 cohort f 8 subjects each. Subjects in both cohorts are randomized in a 3:1 ratio to receive multiple doses of the study drugs, TAKC-02 or Placebo. The safety and tolerability of repeated administration of TAKC-02 for 2 weeks will be evaluated, and the maximum dose of this drug in the next phase will be estimated. Pharmacokinetics will be also analyzed.

Studietyp

Interventionell

Inskrivning (Faktisk)

52

Fas

  • Fas 1

Kontakter och platser

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

Studieorter

      • Tokyo, Japan
        • TAKC-02 Study Site

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

20 år till 40 år (Vuxen)

Tar emot friska volontärer

Ja

Kön som är behöriga för studier

Manlig

Beskrivning

Inclusion Criteria:

  • Both Step 1 and Step 2 are for healthy adult males who meet all of the following conditions.

    1. Subjects are normal healthy men
    2. Aged between 20 and 40 at the time of consent
    3. Subjects who have obtained the voluntary consent of the person in writing
    4. Subjects with BMI of 18.5 or more and less than 25.0 kg / m2
    5. Subjects who can be hospitalized during the cohort transition safety assessment period

Exclusion Criteria:

  • Both Step 1 and Step 2 do not apply to those who meet any of the following conditions.

    1. Subjects with clinically problematic complications or medical history
    2. Subjects with a history of drug allergies
    3. Smokers (those who have smoked within 1 year)
    4. Subjects with hypersensitivity disease (excluding asymptomatic pollinosis)
    5. Those who may affect the absorption, distribution, metabolism and excretion of drugs
    6. Subjects have been prescribed a drug intended for treatment within 4 weeks before administration of the study drug, or those who need administration during the period of participation in the study
    7. Subjects have used over-the-counter drugs within 4 weeks before administration of the study drug, or those who need to use it during the period of participation in the study
    8. Subjects ingested alcoholic beverages or caffeine-containing beverages within 24 hours before administration of the study drug
    9. Subjects with reduced lung function (FEV1.0% <70%)
    10. Subjects with alcoholism or drug addiction
    11. Subjects have a positive reaction in the substance abuse test
    12. Subjects tested positive for HBsAg, hepatitis C virus (HCV) antibody, HIV antigen / antibody, syphilis serum reaction or severe acute respiratory syndrome (SARS)-CoV-2 nucleic acid amplification
    13. Subjects collected 400 mL or more of whole blood within 16 weeks before administration of the study drug or 200 mL or more of blood within 4 weeks, or those who collected component blood (plasma component and platelet component) within 2 weeks before administration of the study drug, or subjects whose annual total blood collection volume exceeds 1200 mL, including the planned blood collection volume for clinical trials
    14. Subjects have been treated with TAKC-02 in the past
    15. Subjects participated in another clinical trial and were administered anther test drug within 16 weeks before the administration of the study drug, or those who participated in another clinical trial at the same time as this clinical trial.
    16. Subjects have been vaccinated against new coronavirus, influenza, etc. within 4 weeks before the administration of the study drug, or who are scheduled to be vaccinated during the period of participation in the study.
    17. Subjects are not willing to adhere to proper contraception using effective contraception for 3 weeks after the last dose of the study drug from the date of admission of study site.
    18. Subjects are judged inappropriate to participate in the clinical trial by the investigator or the co-investigator.

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
Experimentell: Cohort 1
TAKC-02 0.15mg Single dose
Inhalation Solution
Placebo-jämförare: Placebo (to Cohort 1)
Inhalationslösning
Experimentell: Cohort 2
TAKC-02 0.5mg Single dose
Inhalation Solution
Placebo-jämförare: Placebo (to Cohort 2)
Inhalationslösning
Experimentell: Cohort 3
TAKC-02 1.5mg Single dose
Inhalation Solution
Placebo-jämförare: Placebo (to Cohort 3)
Inhalationslösning
Experimentell: Cohort 4
TAKC-02 5mg Single dose
Inhalation Solution
Placebo-jämförare: Placebo (to Cohort 4)
Inhalationslösning
Experimentell: Cohort 5
TAKC-02 15mg Single dose
Inhalation Solution
Placebo-jämförare: Placebo (to Cohort 5)
Inhalationslösning
Experimentell: Cohort 6
TAKC-02 Multiple dose (low)
Inhalation Solution
Placebo-jämförare: Placebo (to Cohort 6)
Inhalationslösning
Experimentell: Cohort 7
TAKC-02 Multiple dose (high)
Inhalation Solution
Placebo-jämförare: Placebo (to Cohort 7)
Inhalationslösning

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Changes in the rate of adverse events
Tidsram: Up to 7 days after dose
assessed by the change in number of adverse events
Up to 7 days after dose

Sekundära resultatmått

Resultatmått
Tidsram
AUC from time zero to the time of the last quantifiable concentration (AUC0-t last)
Tidsram: Up to 48 hours after last dose
Up to 48 hours after last dose
Cmax
Tidsram: Up to 48 hours after last dose
Up to 48 hours after last dose
Tmax
Tidsram: Up to 48 hours after last dose
Up to 48 hours after last dose
T1/2
Tidsram: Up to 48 hours after last dose
Up to 48 hours after last 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 (Faktisk)

17 augusti 2021

Primärt slutförande (Faktisk)

28 december 2021

Avslutad studie (Faktisk)

28 december 2021

Studieregistreringsdatum

Först inskickad

17 augusti 2021

Först inskickad som uppfyllde QC-kriterierna

23 augusti 2021

Första postat (Faktisk)

24 augusti 2021

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

2 juni 2022

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

30 maj 2022

Senast verifierad

1 maj 2022

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • TAKC-02-001

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