Relative Bioavailability Study to Evaluate Cetirizine HCl Gummy 10 mg and Cetirizine HCl Oral Tablets 10 mg

NCT ID: NCT04071821

Last Updated: 2024-06-13

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: PHASE1
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-05-01
• Study Completion Date: 2025-09-30

Brief Summary

A Randomized, Open-Label, Single-Dose, Five-Period Crossover, Relative Bioavailability Study to Evaluate Cetirizine HCl Gummy 10 mg and Cetirizine HCl Oral Tablets 10 mg Administered in Healthy Adult Male and Female Subjects

Detailed Description

Primary:

• To determine the relative bioavailability of a single oral dose of cetirizine HCl Gummy 10 mg and cetirizine HCl oral tablets 10 mg administered under fasted conditions in healthy adult male and female subjects.

Secondary:

• To determine the relative bioavailability of a single oral dose of cetirizine HCl Gummy 10 mg administered under fasted and fed conditions in healthy adult male and female subjects;
• To determine the relative bioavailability of a single oral dose of cetirizine HCl Gummy 10 mg administered under fasted conditions with and without water in healthy adult male and female subjects;
• To determine the relative bioavailability of a single oral dose of cetirizine HCl Gummy 10 mg administered under fasted conditions and chewed or swallowed whole in healthy adult male and female subjects.

Conditions

Allergy

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: OTHER
• Blinding Strategy: NONE

Study Groups

A: Test under Fasted Condition

Single oral dose of cetirizine HCl Gummy 10 mg, chewed, administered with approximately 240 mL of room temperature water, under fasted conditions

Group Type: EXPERIMENTAL

cetirizine HCl Gummy

Intervention Type: DRUG

cetirizine HCl 10mg in a gummy formulation

B: Reference under Fasted Condition

Reference: Single oral dose of cetirizine HCl oral tablets 10 mg, administered with approximately 240 mL of room temperature water, under fasted conditions

Group Type: ACTIVE_COMPARATOR

Zyrtec tablet 10mg

Intervention Type: DRUG

cetirizine HCl 10mg tablet

C: Test under Fed Condition

Test: Single oral dose of cetirizine HCl Gummy 10 mg, chewed, administered with approximately 240 mL of room temperature water, under fed conditions

Group Type: EXPERIMENTAL

cetirizine HCl Gummy

Intervention Type: DRUG

cetirizine HCl 10mg in a gummy formulation

D: Test under Fasted Condition with No Water

Single oral dose of cetirizine HCl Gummy 10 mg, chewed, administered with no water, under fasted conditions

Group Type: EXPERIMENTAL

cetirizine HCl Gummy

Intervention Type: DRUG

cetirizine HCl 10mg in a gummy formulation

E: Test Swallowed Whole with Water, under Fasted Condition

Single oral dose of cetirizine HCl Gummy 10 mg, swallowed whole, administered with approximately 240 mL of room temperature water, under fasted conditions

Group Type: EXPERIMENTAL

cetirizine HCl Gummy

Intervention Type: DRUG

cetirizine HCl 10mg in a gummy formulation

Interventions

cetirizine HCl Gummy

cetirizine HCl 10mg in a gummy formulation

Intervention Type: DRUG

Zyrtec tablet 10mg

cetirizine HCl 10mg tablet

Intervention Type: DRUG

Other Intervention Names

Ceteric Allergy Gummy

Eligibility Criteria

Inclusion Criteria

1. Are capable of giving informed consent and complying with study procedures;

2. Male or female, 18 to 55 years of age, inclusive, at date of consent;

3. Body mass index (BMI) ≥ 18.0 to ≤ 32.0 kg/m2 and total body weight > 50 kg (110 lbs.) at Screening;

4. All female subjects must have a negative pregnancy test at Screening and at each Check-in Visit; and one of the following:

1. Using a medically acceptable form of birth control for at least 1 month prior to first dose [e.g., hormonal contraceptives (oral, patch, injectable or vaginal ring), intrauterine device, or a double barrier method (e.g., diaphragm, cervical cap, oral, patch or vaginal hormonal contraceptive, condom, spermicide, or sponge)]

2. Documented as surgically sterile by hysterectomy, bilateral oophorectomy, bilateral salpingectomy, or bilateral tubal ligation/tubal occlusion) at least 6 months prior to the first dose;

3. Postmenopausal (no menstruation for a minimum of 12 months and confirmed by FSH and estradiol at Screening);

5. Medically healthy based on medical history, vital sign measurements, clinical laboratory test results, and physical examination;

6. Non-smokers (including nicotine-containing products) for at least 6 continuous months prior to the first dose.

7. Be willing and able to consume all contents of the standardized high calorie, high fat breakfast within 30 minutes prior to dosing.

Exclusion Criteria

1. Females who are pregnant, lactating, or planning to become pregnant during the study;

2. Life-time history and/or recent evidence of alcohol or drug/substance abuse disorder;

3. Subjects with history of hypersensitivity to cetirizine or hydroxyzine, or any component of the test and reference formulations;

4. Subjects who test positive at Screening for human immunodeficiency virus (HIV), Hepatitis B surface antigen (HBsAg), or Hepatitis C virus (HCV) antibody;

5. Subjects who test positive at Screening or at Check-in for alcohol and/or drugs of abuse;

6. Subjects who donated ≥ 500 mL of blood within 56 days prior to the first dose of study drug or ≥ 50 mL and ≤ 499 mL of blood within 30 days or plasma (e.g. plasmapheresis) within 14 days prior to the first dose of study drug;

7. Use of prescription or non-prescription drugs, dietary supplements, or herbal supplements at the time of Screening and within 14 days prior to the first dose of the study drug;

8. Subjects who have a history of difficulty in donating blood or difficulty with phlebotomy procedures, and poor venous access;

9. Subjects who have participated in another clinical trial within 30 days prior to the first study period;

10. Member or first-degree relative of study staff or the Sponsor directly involved in the study;

11. Any condition which in the opinion of Investigator would interfere with the subject's ability to provide informed consent, comply with study instructions, confound interpretation of study results, or endanger the subject if he or she took part in the trial.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Seattle Gummy Company

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Provided Documents

Document Type: Study Protocol

View Document

Other Identifiers

P001-2019

Identifier Type: -

Identifier Source: org_study_id