A First-in-Human Study to Learn How Well a Bi-Layer Calcium Carbonate Antacid Tablet Works Compared to a Standard, Non-Layered Calcium Carbonate Tablet in Healthy Male Participants

Healthy Volunteers Clinical Trial

Official title:

An Open Label, Single Center, Randomized, Two-way Crossover Parallel Group, Trial to Assess the Mechanism of Action of a Bi-layer Swallowable Tablet (Immediate Release and Sustained Release) Containing Calcium Carbonate Antacid in an Overnight and Day Application as Compared With a Standard, Non-layered (Immediate Release) Calcium Carbonate Swallow Tablet in Fed Healthy Male Participants.

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06293326
• Other study ID #: 22553
• Status: Recruiting
• Phase: Phase 1
• Start date: March 6, 2024
• Est. completion date: June 6, 2024

Study information

• Verified date: May 2024
• Source: Bayer
• Contact: Bayer Clinical Trials Contact
• Phone: (+)1-888-84 22937
• Email: clinical-trials-contact[@]bayer.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Researchers are looking for a better way to treat people who have heartburn, indigestion, and problems due to excessive stomach acid. These are common problems which can affect daily life and disturb sleep during the night-time. Heartburn is the burning sensation or pain in the chest which occurs when stomach acid rises up in the food pipe (esophagus).

Calcium carbonate tablets are used to treat heartburn, indigestion, and related digestive problems. Calcium carbonate works by neutralizing the excess acid in the stomach. The study treatment is a new bi-layer calcium carbonate tablet that has two layers. One layer quickly releases calcium carbonate aimed to provide quick relief (called immediate release) while the other layer releases calcium carbonate slowly to make the relief last longer (called sustained release).

In this study, bi-layer calcium carbonate tablets will be given to healthy men for the first time. This study will provide information on how the new bi-layer tablet works inside the body.

The main purpose of this study is to learn about how the new bi-layer calcium carbonate tablet changes the average acidity levels (measured using pH) compared to the standard calcium carbonate tablet during the night-time.

For this, researchers will measure the acidity levels in the upper part of the stomach at regular intervals during the night-time.

The participants will be randomly (by chance) assigned to one of two treatment groups:

Participants in the first group will take the treatments at night.

Participants in the second group will take the treatments during the day.

All participants in both groups will take 2 bi-layer tablets and 2 standard tablets after a meal with a gap of 6 to 8 days between treatments. However, in each group, half the participants will receive the bi-layer tablets first while the other half will receive the standard tablets first.

Each participant will be in the study for around 52 days with up to 4 visits to the study site. This includes:

1. visit about 28 days before the treatment starts during which the doctors will confirm that the participant can take part in the study

2. visits for treatment with a gap of 6-8 days between each treatment, and

1 visit 7 to 14 days after the treatment ends during which the doctors will monitor the participants' health.

During the study, the doctors and their study team will:

check participants' overall health by performing tests such as blood and urine tests, and check heart health using an electrocardiogram (ECG)

take images of the stomach at different times after taking the treatment

measure acidity level (pH) using a device called pH probe that is inserted into the upper part of the stomach

ask the participants questions about how easy it is to take the study treatment

ask the participants what adverse events they are having.

An adverse event is any medical problem that a participant has during a study. Doctors keep track of all adverse events, irrespective of whether they think it is related to the study treatment, or not.

As this study is conducted in healthy men who will not gain any benefit from this treatment, access to the study treatment after the study is not planned.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 16
• Est. completion date: June 6, 2024
• Est. primary completion date: June 6, 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Male

• Participant must be 18 to =65 years of age inclusive, at the time of signing the informed consent.

• Participants must have a verified diagnosis of "healthy": the results of the standard clinical, laboratory, and instrumental examinations are within the normal range (limits of reference range). The Investigator can interpret individual findings based on the participant's age, physical state and level of fitness. Participants with readings marginally outside the normal range may be included in the study if, in the Investigator's opinion, these are not clinically significant (NCS); this decision will be documented in the Case Report Form (CRF).

• Results of safety laboratory tests are within normal range (limits of reference range).

• Non-smokers or passive smokers exposed to smoke in an enclosed room for less than 4 h per week.

• Body mass index (BMI) within the range 18.5 to =30 kg/m2 (inclusive).

• Unless participant has had bilateral orchidectomy or a vasectomy (with confirmed sterility), must be abstinent from penile-vaginal intercourse for the duration of the study and agree to remain abstinent for 90 days after the last dose of IMP, OR agree to use a condom during each episode of penile-vaginal intercourse, in addition to their partner (if a person who could become pregnant) using a highly effective form of contraception as described in protocol.

• Participant has given written informed consent to participate in the trial prior to admission to the trial as described in the protocol which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol.

• Be willing and able to participate in all scheduled visits, treatment plan, laboratory tests and other trial procedures according to the protocol.

Exclusion Criteria:

• A history of physical or psychiatric diseases (e.g., diabetes, hypothyroidism and other metabolic diseases, renal disease).

• Recent unexplained significant weight loss (6-7 kg) in the last 6 months.

• A history or current symptoms of Zollinger-Ellison syndrome, gastric carcinoma, peptic ulcer disease, pernicious anaemia, Barrett's oesophagus or systemic sclerosis.

• Meal-induced heartburn of severe severity, historically and -

• Use of any H2-receptor antagonist and/or PPI within one week prior to Screening.

• History and currently prescribed medication for treatment of heartburn associated with increased acidity, reflux esophagitis, and peptic ulcers.

• Current or history of drug or alcohol abuse.

Related Conditions & MeSH terms

• Dyspepsia
• Healthy Volunteers
• Heartburn
• Indigestion

Intervention

Drug:
• bi-layer calcium carbonate tablet (BAY1180654)
Singal dose; two tablets; administered 1-2 hours post standardized meal depending on day or night dosing.
• Immediate release calcium carbonate tablet (BAY1180654)
Singal dose; two tablets; administered 1-2 hours post standardized meal depending on day or night dosing.

Locations

Country	Name	City	State
United Kingdom	BDD Pharma Bio-imaging Unit	Glasgow

Sponsors (1)

Lead Sponsor	Collaborator
Bayer

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Gastric pH levels as measured and recorded with tip of pH probe in gastric fundus.		During night-time on Day 1
Secondary	Gastric pH levels as measured and recorded with tip of pH probe in gastric fundus.		During daytime on Day 1
Secondary	Percentage of total time gastric pH is above pH 3.5 from time of dosing until 8h post-dose during night-time comparing the bi-layer tablet and standard comparator		Up to 8 hours post-dose during night-time
Secondary	Percentage of total time gastric pH is above pH 3.5 from time of dosing until 6h post-dose during daytime comparing the bi-layer tablet and standard comparator.		Up to 6 hours post-dose during daytime
Secondary	Change in mean gastric pH		During night-time and daytime on Day 1
Secondary	Gastrointestinal tract location using scintigraphic images.		During night-time and daytime on Day 1
Secondary	Initial radiolabel release time, using scintigraphic images		During night-time and daytime on Day 1
Secondary	Disintegration rate (t50%) of each formulation will be determined quantitatively via analysis of scintigraphic images.		During night-time and daytime on Day 1
Secondary	Complete radiolabel release time, using scintigraphic images		During night-time and daytime on Day 1
Secondary	Gastric emptying kinetics of the dispersed radiolabeled material (t50% and t90%) of each formulation will be determined quantitatively via analysis of the scintigraphic images.		During night-time and daytime on Day 1
Secondary	Participant questionnaire	The following questions will be asked: PERCEPTIONS Focusing on the sensory experience you have had from the tablet; please indicate how much you agree/disagree with each of the following statements?; This tablet feels like is easy to swallow; This tablet is pleasant to use	On Day 1

External Links

•   Click here to find further information and, after study completion, the study results according to Bayer's transparency standards.