Study to Evaluate the Safety and the Pharmacokinetics of IY-NT-T

Sponsor
Il-Yang Pharm. Co., Ltd. (Industry)
Overall Status
Recruiting
CT.gov ID
NCT05617651
Collaborator
(none)
50
1
2
4.7
10.7

Study Details

Study Description

Brief Summary

This study evaluate the pharmacokinetic and safety of IY-NT-T in healthy adults

Condition or Disease Intervention/Treatment Phase
Phase 1

Detailed Description

Phase 1 study to evaluate the safety and the pharmacokinetics of IY-NT-T in healthy adult volunteers under fed condition

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Masking Description:
In order to prevent distortion (bias) affecting test results during sample analysis, this clinical trial shall not be disclosed to analysis manager and analyst until the specimen analysis is completed.
Primary Purpose:
Treatment
Official Title:
Phase 1 Study to Evaluate the Safety and the Pharmacokinetics of IY-NT-T in Healthy Adult Volunteers Under Fed Condition
Actual Study Start Date :
Oct 27, 2022
Anticipated Primary Completion Date :
Feb 10, 2023
Anticipated Study Completion Date :
Mar 18, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: A group

Period 1 : Ilaprazole 10mg 2Tab, one a day Period 2 : Ilaprazole 20mg 1Tab, one a day Period 3 : Ilaprazole 10mg 2Tab, one a day

Drug: IY-NT-T
Ilaprazole 20mg

Drug: IY-NT-R
Ilaprazole 10mg
Other Names:
  • Noltec(the brand name)
  • Active Comparator: B group

    Period 1 : Ilaprazole 20mg 1Tab, one a day Period 2 : Ilaprazole 10mg 2Tab, one a day Period 3 : Ilaprazole 20mg 1Tab, one a day

    Drug: IY-NT-T
    Ilaprazole 20mg

    Drug: IY-NT-R
    Ilaprazole 10mg
    Other Names:
  • Noltec(the brand name)
  • Outcome Measures

    Primary Outcome Measures

    1. Ilaprazole AUCt [Predose(0hour), after dose 1, 1.5, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 32, 34, 36, 40, 48 hour]

      ilaprazole AUCt(Area under the concentration-time curve)

    2. Ilaprazole Cmax [Predose(0hour), after dose 1, 1.5, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 32, 34, 36, 40, 48 hour]

      ilaprazole Cmax(Maximum concentration of drug in plasma)

    Secondary Outcome Measures

    1. Ilaprazole AUC∞ [Predose(0hour), after dose 1, 1.5, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 32, 34, 36, 40, 48 hour]

      ilaprazole AUC∞(Area under the plasma drug concentration-time curve from time 0 to infinity)

    2. Ilaprazole tmax [Predose(0hour), after dose 1, 1.5, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 32, 34, 36, 40, 48 hour]

      ilaprazole tmax(Time to maximum plasma concentration)

    3. Ilaprazole t1/2 [Predose(0hour), after dose 1, 1.5, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 32, 34, 36, 40, 48 hour]

      ilaprazole t1/2(Terminal elimination half-life)

    4. Ilaprazole tmax-tlag [Predose(0hour), after dose 1, 1.5, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 32, 34, 36, 40, 48 hour]

      Ilaprazole tmax-tlag (Time to maximum plasma concentration minus Lag time)

    5. Ilaprazole intra-subject tlag difference [Predose(0hour), after dose 1, 1.5, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 32, 34, 36, 40, 48 hour]

      Ilaprazole intra-subject Lag time difference

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    19 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    1. Volunteers aged 19 years and above at screening

    2. A volunteer who weighs ≥ 50kg (≥ 45kg for women) and has a body mass index(BMI)* of ≥18.0 and ≤ 30 at screening

    *BMI(body mass index, kg/m^2)= Body weight (kg)/[height (m)^2]

    1. A volunteer who has no congenital or chronic diseases, no pathological symptoms, or findings from medical examination at screening

    2. A volunteer who is determined by the principal investigator or sub-investigator(responsible physician) as eligible as a subject based on diagnostic tests( hematology, hematochemical, serum, urinalysis) and electrocardiogram tests established and conducted according to the characteristics of the study drug

    3. A volunteer and their spouse or partner, who agree to use a medically appropriate method of contraception to exclude potential of pregnancy and not to provide sperm or ova from the first dose to 7 days after the last dose of study drug

    • Contraception methods: Intrauterine device, vasectomy, tubal ligation and contraceptive barrier methods (male condoms, women condoms, cervical caps. Contraceptive diaphragm, sponge,etc) used in combination or if spermicide is used, two or more contraceptive barrier methods
    1. A volunteer who voluntarily provided written consent to participation in the entire study process after being fully informed of the study objective, contents, characteristics of the study drugs, and expected adverse reactions, prior to study participation
    Exclusion Criteria:
    1. A volunteer who has a history or present symptoms of clinically significant disorders relating to any of the following: digestive system, cardiovascular system, endocrine system, respiratory system, blood and lymphatic, infectious disease, renal, urinary, and reproductive, system, nervous system, musculoskeletal system, immune system, otolaryngology, skin and subcutaneous tissue system, and ophthalmic system

    2. A volunteer who has a history of gastrointestinal surgery that may affect drug absorption (except simple appendectomy or hernia surgery) or has gastrointestinal diseases

    3. A volunteer who has taken drugs that induce or inhibit drug metabolizing enzymes such as barbiturates within 1 month prior to the first dose or who has taken drugs that may interfere with clinical study within 10 days prior to the first dose(Provided that, participation may be considered based on drug-drug interaction, pharmacokinetics and pharmacodynamics(such as half-life) of study drug)

    4. A volunteer who has participated in other clinical trials or bioequivalence studies within 6 months prior to the first dose of the study drug

    5. A volunteer who has participated in whole blood donation within 8 weeks prior to first dose, or apheresis donation within w weeks prior to first dose, or received blood donation within 4 weeks prior to first dose.

    6. A volunteer that meets any of the following conditions within 1 month prior to first dose

    • Average alcohol intake(for men): > 21 glass/week

    • Average alcohol intake(for women): > 14 glass/week (1 glass = 50ml of soju or 30ml of liquor, or 250ml of beer)

    • Average cigarette smoking: > 20 cigarettes per day.

    1. A volunteer that meets any of the following categories
    • Volunteer who is hypersensitive to the active ingredient or other ingredients of this drug
    1. Patients that meet any of the following conditions
    • Gastric ulcer patients possibly related to a malignant tumor

    • Hepatic disorder or renal disorder patients

    • Patients receiving Atazanavir

    • Patients receiving Rilpivirine-containing products

    1. A volunteer who is considered by the investigator to be ineligible to participate in this study for other reasons

    2. Pregnant or nursing women

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 H plus Yangji Hospital Seoul Gwanak-gu Korea, Republic of 08756

    Sponsors and Collaborators

    • Il-Yang Pharm. Co., Ltd.

    Investigators

    • Principal Investigator: Jae Woo Kim, MD, PhD, H Plus Yangji Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Il-Yang Pharm. Co., Ltd.
    ClinicalTrials.gov Identifier:
    NCT05617651
    Other Study ID Numbers:
    • DTC22-IP018
    First Posted:
    Nov 15, 2022
    Last Update Posted:
    Nov 15, 2022
    Last Verified:
    Nov 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Il-Yang Pharm. Co., Ltd.

    Study Results

    No Results Posted as of Nov 15, 2022