Bioequivalence Study of Ezetimibe Tablets Under Fed Conditions in Healthy Subjects

Qingdao University

Status and phase: Invitation-only; Phase 1

Conditions: Safety; Pharmacokinetics

Treatments: Behavioral: Test Preparation-Reference preparation-Reference preparation; Behavioral: Reference preparation-Test Preparation-Reference preparation; Behavioral: Reference preparation-Reference preparation-Test Preparation

Study type: Interventional

Funder types: Other

Identifiers

NCT05481385

22FWX-CZYZ-005-01

Details and patient eligibility

About

The fed bioequivalence test adopts the experimental design of single center, single oral administration, random, open, two sequence, two cycle crossover and self-control.

Full description

To investigate the in vivo pharmacokinetic characteristics of ezetimibe tablets (specification 10mg) in Chinese healthy subjects after a single oral administration under fed conditions, and to evaluate the bioequivalence of ezetimibe tablets produced by Changzhou Pharmaceutical Factory Co., Ltd. and the licensee MSD Pharma (Singapore) PTE. Ltd. To study the safety of single oral ezetimibe tablets (specification 10mg) in Chinese healthy subjects.

Enrollment: 48 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• • Healthy male or female aged 18 and above.

  • The body mass index is in the range of 18.6-28.5 kg/m2 (including the critical value). The weight of male is not less than 50.0 kg, and that of female is not less than 45.0 kg.
  • The following examination show that the indicators are normal or abnormal without clinical significance. The examination including: Vital signs, physical examination, blood routine, blood biochemistry, urinalysis, pregnancy test for female, serological tests for hepatitis B virus, hepatitis C virus, human immunodeficiency virus (HIV), and syphilis virus, 12 lead ECG, breath test for alcohol, drug abuse test.
  • The subjects have no family planning within 3 months and could select contraceptive method.
  • Before the study, all subjects have been informed of the study's purpose, protocal, benefits, and risks, and signed the informed consent voluntarily.

Exclusion criteria

• • Being allergy to the study medications, smoking, alcohol abuse.

  • Participation in another clinical trial within 3 months.

Trial design

Primary purpose: Other

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: None (Open label)

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48 participants in 2 patient groups

Test preparation

Experimental group

Description:

Ezetimibe tablets: specification: 10mg; Package specification: 7 pieces / plate, 1 plate / box; Produced and provided by Changzhou Pharmaceutical Factory Co., Ltd.

Treatment:

Behavioral: Test Preparation-Reference preparation-Reference preparation

Reference preparation

Active Comparator group

Description:

Ezetimibe Tablets Ezetrol ®; Specification: 10mg, packaging specification: 10 pieces / plate, 1 plate / box; Licensee: MSD Pharma (Singapore) PTE. Ltd

Treatment:

Behavioral: Reference preparation-Reference preparation-Test Preparation

Behavioral: Reference preparation-Test Preparation-Reference preparation