check_circleStudy Completed

Contrast enhancement in magnetic resonance imaging, Healthy volunteers

Bayer Identifier:

19730

ClinicalTrials.gov Identifier:

Not Available

EudraCT Number:

Not Available

EU CT Number:

Not Available
A study to learn more about the safety and the blood level of BAY1747846 given as injection into the vein at increasing single doses in Chinese healthy male participants

Trial purpose

The goal of this clinical study was to learn more about BAY1747846 compared to placebo when given as an injection into the vein in Chinese healthy male participants:
- the safety of BAY1747846 when given at increasing single doses
- the level of BAY1747846 in the blood over time when given at increasing single doses.
To answer the first question, the researchers compared the number and severity of medical problems the Chinese participants had after receiving BAY1747846 at increasing doses and placebo respectively. Doctors kept tracking of all medical problems that happened in the study, even if they did 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 blood, also called AUC
- the (average) highest level of BAY1747846 in the blood, also called Cmax
- how BAY1747846 is removed from the blood, also called clearance (CL).

Key Participants Requirements

Sex

Male

Age

18 - 45 Years
  • - Signed informed consent prior to any study specific tests or procedures
    - Chinese male between 18 and 45 years (inclusive) at screening visit
    - Body mass index (BMI): 18.5 to 30.0 kg/m² (inclusive)
    - Body weight (bw): 50 to 90 kg (inclusive)
    - Participants of reproductive potential must agree to use adequate contraception whenever having sexual intercourse with a woman of child-bearing potential. This applies for the time period from signing of the ICF to at least 1 week after treatment. The definition of adequate contraception will be based on the judgment of the investigator and on local requirements
    - Healthy, based on medical history, physical examination, electrocardiography (ECG), and laboratory tests
  • - Use of systemic or topically active medication or herbal remedies, prescription or non-prescription, from screening to the first drug administration (only use of contraceptives and occasional use of paracetamol, aspirin or ibuprofen is permissible)
    - Any severe disease within the last 4 weeks prior to the first study drug administration
    - Any clinically relevant finding at the physical examination and chest X ray (posterior-anterior) examination
    - 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
    - Vital signs: Pulse rate <50 or >90beats/min, Systolic blood pressure <100 or ≥140 mmHg, Diastolic blood pressure <60 or ≥90 mmHg, or other abnormal vital signs
    - Any known disposition for allergic, anaphylactoid, hypersensitivity or idiosyncratic reactions, e.g. any history of clinical signs of hypersensitivity reaction to any agent (including, but not limited to, any allergen, food, drug, chemical, or contrast agent)
    - Family history of hypersensitivity reaction to contrast agent
    - Regular alcohol consumption equivalent to >20 g alcohol per day within 3 months prior to screening
    - Smokers who smoke more than 5 cigarettes per day within 3 months prior to screening and/or who cannot refrain from smoking from screening until the end of hospitalization
    - Criteria which in the opinion of the investigator preclude participation for scientific reasons, for reasons of compliance, or for reasons of the participant's safety

Trial summary

Enrollment Goal
24
Trial Dates
August 2020 - April 2021
Phase
Phase 1
Could I Receive a placebo
No
Products
Gadoquatrane (BAY1747846)
Accepts Healthy Volunteer
Yes

Where to participate

StatusInstitutionLocation
Completed
Beijing HospitalBeijing, 100730, China

Primary Outcome

  • Number of participants with treatment-emergent adverse events (TEAE)
    Including severity of TEAE
    date_rangeTime Frame:
    From drug administration up to 7 days after end of test drug administration (from day 1 to day 8)

Secondary Outcome

  • Cmax
    Cmax: Maximum observed drug concentration in measured matrix after single dose administration
    date_rangeTime Frame:
    Pre-dose, on Day 1, Day 2, Day 3 and Day 4
  • AUC
    AUC: Area under the concentration vs. time curve from zero to infinity after single dose in case AUC cannot be determined reliably for all participants, AUC will be replaced by AUC(0-tlast)
    date_rangeTime Frame:
    Pre-dose, on Day 1, Day 2, Day 3 and Day 4
  • CL
    CL: Total body clearance of drug
    date_rangeTime Frame:
    Pre-dose, on Day 1, Day 2, Day 3 and Day 4
  • CL/bw
    CL/bw: Total body clearance of drug normalized by body weight
    date_rangeTime Frame:
    Pre-dose, on Day 1, Day 2, Day 3 and Day 4.

Trial design

Randomized, single-blind, placebo-controlled, escalating single-dose study of safety, tolerability, and pharmacokinetics of intravenously administered BAY 1747846 in healthy Chinese men
Trial Type
Interventional
Intervention Type
Drug
Trial Purpose
Other
Allocation
Randomized
Blinding
N/A
Assignment
Parallel Assignment
Trial Arms
2

Additional Information

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