Study to Evaluate the Bioequivalence of Vonopzan Tablet 20mg(Vonoprazan Fumarate) and Vocinti Tablet 20mg in Healthy Adult Subjects.

NCT06642987 | Completed Phase 1

• 1 other identifier: DDS23-018BE
• Study Type: interventional
• Target: 30
• Locations: 1 country
• Sites: 1

Brief Summary

This clinical trial is an open-label, randomized, fasting, single-dose, two-sequence, two-period, crossover study in healthy subjects to evaluate the bioequivalence of "Vonopzan Tablets 20 mg(Vonoprazan Fumarate)" of Hanlim Pharm.l Co., Ltd. and "Vocinti Tablet 20 mg (Vonoprazan Fumarate)" of Takeda Pharmaceuticals Korea Co., Ltd. in Healthy Adult Subjects.

Conditions

Gastric Ulcer

Outcome Measures

Primary Outcomes (2)

• Peak Plasma Concentration (Cmax)

  Concentration of vonoprazan in plasma

  36 hours

• Area under the plasma concentration versus time curve (AUC)

  Concentration of vonoprazan in plasma

  36 hours

Secondary Outcomes (4)

• AUCt/AUC∞

  36 hours

• Half life

  36 hours

• Tmax

  36 hours

• AUC ∞

  36 hours

Study Arms (2)

Vonoprazan Test 20mg

EXPERIMENTAL

On the day of the visit, take 1 tablet of the experimental drug orally with 150 mL of water around 8 am.

Drug: Vonoprazan Test 20mg

Vonoprazan Reference 20mg

ACTIVE COMPARATOR

On the day of the visit, take 1 tablet of the comparator drug orally with 150 mL of water around 8 am.

Drug: Vonoprazan Reference 20mg

Interventions

Vonoprazan Test 20mg DRUG

1 tablets orally once a day

Also known as: vonoprazan fumarate

Vonoprazan Test 20mg

Vonoprazan Reference 20mg DRUG

1 tablets orally once a day

Also known as: Vonoprazna fumarate

Vonoprazan Reference 20mg

Eligibility Criteria

• Age: 19 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Individuals aged 19 years or older at the time of screening
• Individuals with no clinically significant congenital or chronic diseases and no pathological symptoms or findings based on medical examinations (such as EEG, ECG, chest and gastric endoscopy, or gastrointestinal radiology tests, if necessary)
• Individuals deemed suitable for the study based on screening tests (e.g., hematology, blood chemistry, serology, and urinalysis) as determined by the principal investigator (or a designated sub-investigator)
• Individuals with a Body Mass Index (BMI) between 18.0 and 30.0 (BMI calculation: weight (kg) / height (m)²)
• Individuals with no history of gastrointestinal surgery that could affect drug absorption.
• Individuals who, after receiving a detailed explanation of the clinical trial, fully understand the study, voluntarily decide to participate, and agree in writing to comply with the trial requirements during the study period.

You may not qualify if:

• Individuals who have taken enzyme-inducing or inhibiting drugs such as barbiturates within 30 days before the start of the study (first dosing day) or medications that might interfere with the study within 10 days before the start of the study (first dosing day)
• Individuals who have engaged in excessive alcohol consumption within one month before the start of the study (first dosing day)
• For men, more than an average of 21 drinks per week
• For women, more than an average of 14 drinks per week (One drink: 45 mL of distilled spirits or 360 mL of beer or 150 mL of wine)
• Individuals who have taken any medication that may interfere with the trial within 10 days prior to the start of the trial (first dose).
• Individuals who have participated in clinical trials (including bioequivalence studies) and received investigational drugs within six months before the start of the study (first dosing day)
• Individuals who have donated whole blood within 8 weeks or donated blood components within 2 weeks before the start of the study (first dosing day)
• Patients with the following conditions:
• Hypersensitivity to the components of this drug
• Currently taking medications containing atazanavir, nelfinavir, or rilpivirine.
• Individuals with a history of mental illness
• Women who may be pregnant, pregnant women, or brestfeeding women
• Individuals who do not agree to use medically recognized dual contraception\* methods, excluding hormonal contraceptives, to prevent pregnancy from the first administration of the investigational drug until one week after the last administration of the investigational drug.
• \- Medically recognized dual contraception methods: Combining intrauterine devices (IUD, IUS), vasectomy, tubal ligation, and barrier methods of contraception (male condom, female condom, cervical cap, diaphragm, sponge, etc.), or using two or more barrier methods in combination with spermicides.

Sponsors & Collaborators

• Hanlim Pharm. Co., Ltd.: lead

Study Sites (1)

Seok Gyeong Medical Foundation Central Hospital

Siheung-si, South Korea

Location

MeSH Terms

Conditions

Stomach Ulcer

Condition Hierarchy (Ancestors)

Peptic Ulcer; Duodenal Diseases; Intestinal Diseases; Gastrointestinal Diseases; Digestive System Diseases; Stomach Diseases

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: OTHER
• Intervention Model: CROSSOVER
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: October 14, 2024
• First Posted: October 15, 2024
• Study Start: October 23, 2023
• Primary Completion: November 3, 2023
• Study Completion: February 23, 2024
• Last Updated: October 16, 2024

Record last verified: 2024-10

Locations

KR (1)