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Completed

NCT Number: NCT06125366

A Study to Learn More About the Safety and the Level of BAY 1747846 in Body Given as Injection Into the Vein at Increasing Single Doses in Japanese Healthy Male Participants

The goal of this clinical study was to learn more about BAY1747846 compared to placebo when given as an injection into the vein in Japanese healthy male participants:

* the safety of BAY1747846 when given at increasing single doses * the level of BAY1747846 in the body over time when given at increasing single doses.

To answer the first question, the researchers compared the number and severity of medical problems the Japanese participants had after receiving BAY 1747846 at increasing doses and placebo respectively. Doctors keep track of all medical problems that happen in studies, even if they do not think they might be related to the study treatments.

To answer the second question, the researchers determined:

* the (average) total level of BAY1747846 in the body, also called AUC * the (average) highest level of BAY1747846 in the body, also called Cmax * how BAY1747846 is removed from the body, also called clearance (CL).

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Key information

Conditions

Contrast Enhancement in Magnetic Resonance Imaging Healthy Volunteers

Age range

20 year–40 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

SOUSEIKAI Fukuoka Mirai Hospital

Fukuoka, 813-0017, Japan

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Signed informed consent prior to any study specific tests or procedures
  • Ability and willingness to understand and follow study-related instructions
  • Subject is healthy as determined by the investigator
  • Japanese male
  • Age 20 to 40 years (inclusive) at screening visit
  • Body mass index (BMI): 18.0 to 28.0 kg/m^2(inclusive)
  • Body weight: at least 50 kg (inclusive)
  • Subjects of reproductive potential must agree to use condoms whenever having sexual intercourse with a woman of child-bearing potential. This applies to the time period from signing of the ICF to at least 1 week after treatment.

Exclusion criteria

  • Current smoker, or has smoked within 3 months prior to screening Clinical Study Protocol
  • Any severe disease within the last 4 weeks prior to administration of study drug
  • History of orthostatic hypotension, fainting spells and blackouts
  • Any malignant tumor and history thereof
  • Any clinically relevant finding at the physical examination
  • Any known disposition for allergic, anaphylactoid, hypersensitivity or idiosyncratic reactions, e.g. any history of clinical signs of hypersensitivity reaction to any contrast agent
  • Any clinically relevant deviation from reference ranges of the laboratory parameters at screening or alanine aminotransferase (ALT), aspartate aminotransferase (AST), bilirubin exceeding the Upper limit of normal range (ULN) by more than 10%, or creatinine above the ULN, or hemoglobin below 12 g/dL
  • Clinically relevant ECG findings, e.g.: Heart rate <45 or > 90 beats/min, PR >220 msec, QTcF >450 msec, QRS >120 msec, branch bundle block, any sign of coronary heart disease at screening

-. Abnormal vital signs, e.g.: Systolic blood pressure <90 or >140 mmHg, Diastolic blood pressure <45 or >90 mmHg at screening

  • Subjects who have participated in a clinical study of an investigational drug within 4 months or an approved drug within 3 months prior to administration of study drug

Treatment and study plan

BAY1747846

Drug

Single dose; IV injection.

Matching Placebo

Drug

Single dose; IV injection.

Primary outcomes

  1. Number of participants with treatment-emergent adverse events

    Time frame: Up to 7 to 10 days after study drug administration (From the time of signing of the ICF until the last visit of follow-up.)

  2. Severity of treatment-emergent adverse events

    Time frame: Up to 7 to 10 days after study drug administration (From the time of signing of the ICF until the last visit of follow-up.)

Secondary outcomes

  1. Maximum observed drug concentration in measured matrix after single dose administration (Cmax)

    Time frame: Pre-dose, on Day 1, Day 2, Day 3 and Day 4.

  2. Area under the concentration vs. time curve from zero to infinity after single dose (AUC)

    Time frame: Pre-dose, on Day 1, Day 2, Day 3 and Day 4.

  3. Total body clearance of drug (CL)

    Time frame: Pre-dose, on Day 1, Day 2, Day 3 and Day 4.

  4. Total body clearance of drug normalized by body weight (CL/bw)

    Time frame: Pre-dose, on Day 1, Day 2, Day 3 and Day 4.

Sponsors and collaborators

Lead sponsor

Bayer

Industry

Registry information

Official study title

Randomized, Single-blind, Placebo-controlled, Escalating Single-dose Study to Investigate Safety, Tolerability, and Pharmacokinetics of Intravenously Administered BAY 1747846 in Japanese Healthy Male Subjects

Important dates

Study start
2019
Primary completion
2019
Study completion
2019
First posted
Nov 9, 2023
Registry last updated
Nov 9, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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