Study on the Safety of the Drug BAY2395840 at Different Doses, the Way the Body Absorbs, Distributes and Excretes the Drug Including the Effect of Its Formulation (Tablet or Liquid) and the Effect of Food on the Absorption, Distribution or Excretion of the Drug in Healthy Male Participants

Bayer

Status and phase: Completed; Phase 1

Conditions: Endometriosis

Treatments: Drug: Placebo tablet; Drug: BAY2395840 tablet; Drug: BAY2395840 oral solution; Drug: Placebo oral solution

Study type: Interventional

Funder types: Industry

Identifiers

NCT05517746

19634

2019-002573-65 (EudraCT Number)

Details and patient eligibility

About

Researchers are looking for a better way to treat people who have endometriosis, a condition in which tissue similar to the lining of the uterus starts to grow in places outside of the uterus. The study treatment, BAY2395840, is being developed to help block certain proteins from causing inflammation and pain in people with endometriosis. But, this is the first time that researchers will study BAY2395840 in humans.

In this study, the researchers will learn how safe BAY2395840 is for the participants to take. They will also learn what happens to BAY2395840 in the body. The study will include about 56 healthy adult men.

All of the participants will take increasing doses of BAY2395840, or a placebo. A placebo looks like a treatment but does not have any medicine in it. Some of the participants will take their study treatment 1 time under diet 1 conditions. The other participants will take their study treatment 7 times with diet 1 or diet 2.

The participants will take BAY2395840 or the placebo as tablets or as a liquid by mouth. The participants will stay at the study site for up to 11 days . After that, they will visit the study site 1 more time. Each participant will be in the study for up to about 14 weeks.

During the study, the doctors will collect blood and urine samples and check the participants' overall health and heart health. The participants will answer questions about how they are feeling, what medications they are taking, and 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 that happen in studies, even if they do not think the adverse events might be related to the study treatments.

Enrollment: 63 patients

Sex: Male

Ages: 18 to 45 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Male participants of age 18 to 45 years (inclusive), at the time of signing the informed consent.
• Body mass index (BMI) ≥18 kg/m^2 and ≤30 kg/m^2.
• Participants who are overtly healthy.
• Race: White.
• Male participants of reproductive potential who are sexually active must agree to use contraception methods.

Exclusion criteria

• Any findings from the medical examination (including medical history, physical examination, vital signs, laboratory tests and ECG) deviating from normal and deemed to be of clinical relevance by the investigator.
• Any known disease that was forbidden in the study as specified in study protocol.
• Any medication or drug use that was forbidden in the study as specified in study protocol.
• Any abnormal finding in Electrocardiogram (ECG), blood pressure or heart rate.
• Any clinical relevant deviation from normal range of laboratory parameters at screening.
• History of COVID-19.
• Prior contact with SARS-CoV-2 positive person or COVID-19 patient within the last 4 weeks prior admission to the ward.
• Positive SARS-CoV-2 viral RNA test.

Trial design

Primary purpose: Basic Science

Allocation: Randomized

Interventional model: Sequential Assignment

Masking: Quadruple Blind

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63 participants in 12 patient groups, including a placebo group

Group 1

Experimental group

Description:

Participants received BAY2395840 dose A as tablets under diet 1 conditions (Period 1). After the safety assessment for Period 1 and a washout period of at least 14 days participants were re-dosed with the same BAY2395840 dose A1 as oral solution under diet 1 conditions (Period 2)

Treatment:

Drug: BAY2395840 tablet

Drug: BAY2395840 oral solution

Group 2

Experimental group

Description:

Participants received BAY2395840 dose C as tablets under diet 1 conditions.

Treatment:

Drug: BAY2395840 tablet

Group 3

Experimental group

Description:

Participants received BAY2395840 dose E as tablets under diet 1 conditions.

Treatment:

Drug: BAY2395840 tablet

Group 4

Experimental group

Description:

Participants received BAY2395840 dose H as tablets under diet 1 conditions

Treatment:

Drug: BAY2395840 tablet

Group 5

Experimental group

Description:

Participants received BAY2395840 dose B as tablets on Day 1 after diet 2, on Days 2 to 7 under diet 1 conditions

Treatment:

Drug: BAY2395840 tablet

Group 6

Experimental group

Description:

Participants received BAY2395840 dose C as tablets on Day 1 after diet 2, on Days 2 to 7 under diet 1 conditions

Treatment:

Drug: BAY2395840 tablet

Group 7

Experimental group

Description:

Participants received BAY2395840 dose I as tablets under diet 1 conditions

Treatment:

Drug: BAY2395840 tablet

Group 8

Experimental group

Description:

Participants received BAY2395840 dose G as tablets on Day 1, followed by 3 BAY395840 doses of dose F as tablets on Days 2 to 4 and subsequently 7 further BAY395840 doses of dose G as tablets on Days 5 to 11 under diet 1 conditions

Treatment:

Drug: BAY2395840 tablet

Placebo matching Group 1

Placebo Comparator group

Description:

Participants received a dose of placebo as tablets under diet 1 conditions (Period 1). After the safety assessment for Period 1 and a washout period of at least 14 days participants were re-dosed with a single dose of placebo as oral solution under under diet 1 conditions (Period 2)

Treatment:

Drug: Placebo tablet

Drug: Placebo oral solution

Placebo matching Group 2 to 4 and Group 7

Placebo Comparator group

Description:

Participants received a dose of Placebo as tablets under diet 1 conditions

Treatment:

Drug: Placebo tablet

Placebo matching Group 5 and 6

Placebo Comparator group

Description:

Participants received Placebo as tablets on Day 1 after diet 2, on Days 2 to 7 under diet 1 conditions

Treatment:

Drug: Placebo tablet

Placebo matching Group 8

Placebo Comparator group

Description:

Participants received a dose of Placebo as tablets on Day 1, followed by 3 doses of Placebo as tablets on Days 2 to 4 and subsequently 7 further doses of Placebo as tablets on Days 5 to 11 under diet 1 conditions.

Treatment:

Drug: Placebo tablet