Scintigraphy Study to Compare the Antireflux Activity of the Z0063 Versus Gaviscon Double Action Tablets, in Healthy Adult Subjects

NCT ID: NCT03065816

Last Updated: 2022-04-25

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 34 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-02-09
• Study Completion Date: 2017-05-02

Brief Summary

Primary Objective:

Pharmacodynamics: assessment and comparison by gamma scintigraphy of the gastric retention of alginate rafts (raft performance) of Z0063 to the effect of Gaviscon Double Action Tablets, in healthy adult subjects.

Secondary Objective:

Safety: assessment of the clinical safety of Z0063 versus Gaviscon Double Action tablets, in healthy adult subjects.

Detailed Description

The total study duration per subject is 37 days including a screening period up to 21 days, a wash-out period of 4-7 days and a follow-up of 4-7 days.

Conditions

Gastroesophageal Reflux Disease

Study Design

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

Study Groups

Sequence 1 (Z0063 to Gaviscon)

The subjects will be given Z0063 single dose and then will crossover to Gaviscon single dose

Group Type: EXPERIMENTAL

Z0063

Intervention Type: DRUG

Pharmaceutical form: chewable tablets Route of administration: oral

Gaviscon

Intervention Type: DRUG

Pharmaceutical form: chewable tablets Route of administration: oral

Sequence 2 (Gaviscon to Z0063)

The subjects will be given Gaviscon single dose and then will crossover to Z0063 single dose

Group Type: EXPERIMENTAL

Z0063

Intervention Type: DRUG

Pharmaceutical form: chewable tablets Route of administration: oral

Gaviscon

Intervention Type: DRUG

Pharmaceutical form: chewable tablets Route of administration: oral

Interventions

Z0063

Pharmaceutical form: chewable tablets Route of administration: oral

Intervention Type: DRUG

Gaviscon

Pharmaceutical form: chewable tablets Route of administration: oral

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Male or female subjects, between 18 and 55 years of age, inclusive.
• Body weight between 50.0 and 100.0 kg, inclusive, if male, and between 40.0 and 90.0 kg, inclusive, if female, body mass index between 18.0 and 28.0 kg/m^2, inclusive.
• Certified as healthy by a comprehensive clinical assessment.
• Normal vital signs, electrocardiogram (ECG) and laboratory parameters.
• Subject has to be willing to eat the standard radiolabelled meal (eggs on toasts and orange juice).

Exclusion Criteria

• Any history or presence of clinically relevant abnormalities at screening which could interfere with the objectives of the study or the safety of the subject's participation.
• Blood donation of more than 450 mL within 3 months before inclusion.
• History or presence of drug or alcohol abuse.
• Smoking more than 5 cigarettes or equivalent per day, unable to stop smoking during the study.
• If female, pregnancy (defined as positive beta-human chorionic gonadotropin [β-HCG] blood test), breast-feeding.
• Any medication (including St John's Wort) within 14 days before inclusion with the exception of hormonal contraception or menopausal hormone replacement therapy.
• Any subject in the exclusion period of a previous study: participation in a new chemical entity clinical study within the previous 3 months or a marketed drug clinical study within the previous 30 days.
• Any subject who cannot be contacted in case of emergency.
• Positive result on any of the following tests: hepatitis B surface (HBs Ag) antigen, anti-hepatitis C virus (anti-HCV) antibodies, anti-human immunodeficiency virus 1 and 2 antibodies (anti-HIV1 and anti HIV2 Ab).
• Positive result on urine drug screen.
• Positive alcohol test.
• Known hypersensitive to alginates, products or formulation excipients and/or to any component of the standardized meal.
• Any subject with difficulty in chewing and/or swallowing.
• Participation in a study in which radioisotopes were administered or in which subject was exposed to any radiation other than normal background radiation within the 12 months before the screening visit.
• Any intake of aluminum and magnesium containing antacids or other alginate-containing medicinal products within 14 days before inclusion.

The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

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

Sponsors

Sanofi

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Clinical Sciences & Operations

Role: STUDY_DIRECTOR

Sanofi

Locations

Investigational site 826001

Merthyr Tydfil, , United Kingdom

Countries

United Kingdom

Other Identifiers

2015-000764-34

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

U1111-1182-1864

Identifier Type: OTHER

Identifier Source: secondary_id

PDY14363

Identifier Type: -

Identifier Source: org_study_id