A Study of JNJ-75105186 in Healthy Japanese and Chinese Participants
Study Details
Study Description
Brief Summary
The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics (PK) of JNJ-75105186 after single ascending oral dose administration in healthy Japanese participants and after single oral dose administration in healthy Chinese participants.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 1 |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Part 1: Single Ascending Dose (SAD) Cohorts Healthy Japanese participants will receive JNJ-75105186 or matching placebo orally in Cohorts 1-3. |
Drug: JNJ-75105186
JNJ-75105186 will be administered orally in Part 1 and 2.
Other: Placebo
Matching placebo to JNJ-75105186 will be administered orally in Parts 1 and 2.
|
| Experimental: Part 2: Single Dose (SD) Cohort Healthy Chinese participants will receive JNJ-75105186 or matching placebo orally in Cohort 4. |
Drug: JNJ-75105186
JNJ-75105186 will be administered orally in Part 1 and 2.
Other: Placebo
Matching placebo to JNJ-75105186 will be administered orally in Parts 1 and 2.
|
Outcome Measures
Primary Outcome Measures
- Part 1 and 2: Number of Participants with Adverse Events as a Measure of Safety and Tolerability [Up to 6 weeks]
An AE is any untoward medical occurrence in a participant participating in a clinical study that does not necessarily have a causal relationship with the pharmaceutical/biological agent under study.
- Part 1 and 2: Plasma Concentration of JNJ-75105186 [Predose up to 48 hours postdose (up to Day 3)]
Plasma samples will be analyzed to determine concentrations of JNJ-75105186 using a validated, specific and sensitive method.
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Healthy on the basis of physical examination, medical history, vital signs, and 12-lead electrocardiogram (ECG) performed at screening. If there are abnormalities, they must be consistent with the underlying illness in the study population. This determination must be recorded in the participant's source documents and initialed by the investigator
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Healthy on the basis of clinical laboratory tests performed at screening. If the results of the serum chemistry panel including liver enzymes, other specific tests, blood coagulation, hematology, or urinalysis are outside the normal reference ranges, the participant may be included only if the investigator judges the abnormalities or deviations from normal to be not clinically significant or to be appropriate and reasonable for the population under study. This determination must be recorded in the participant's source documents and initialed by the investigator
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Body weight not less than 50 kilograms (kg) and body mass index within the range 18 to 30 kg per meter square (kg/m^2) (inclusive)
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A woman must agree not to donate eggs (ova, oocytes) or freeze for future use for the purposes of assisted reproduction during the study and for at least 90 days after receiving the administration of study intervention
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Must sign an informed consent form (ICF) indicating they understand the purpose of, and procedures required for, the study and is willing to participate in the study
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It is recommended that participants are up to date on age-appropriate vaccinations prior to screening as per routine local medical guidelines. For study participants who received locally-approved (and including emergency use-authorized) Coronavirus Disease of 2019 (COVID-19) vaccines recently prior to study entry, follow applicable local vaccine labeling, guidelines, and standards of care for participants receiving immune-targeted therapy when determining an appropriate interval between vaccination and study enrollment
Exclusion Criteria:
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Had major surgery, (example, requiring general anesthesia) within 3 months before screening, or will not have fully recovered from surgery, or has surgery planned during the time the participant is expected to participate in the study or within 12 weeks after the last dose of study intervention administration
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History of surgical resection of the stomach, small or large intestine (excluding appendectomy, cholecystectomy, or resection of benign polyps)
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History of bleeding associated with procedures such as endoscopy or phlebotomy; or use of medications such as nonsteroidal anti-inflammatory drugs or aspirin within 28 days prior to screening or planned use during the study
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Preplanned surgery or procedures that would interfere with the conduct of the study
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Clinically significant infection within 30 days prior to screening or any serious infection within 6 months prior to screening requiring intravenous antimicrobial therapy
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Souseikai Fukuoka Mirai Hospital | Fukuoka-shi | Japan | 813-0017 |
Sponsors and Collaborators
- Janssen Pharmaceutical K.K.
Investigators
- Study Director: Janssen Pharmaceutical K.K., Japan Clinical Trial, Janssen Pharmaceutical K.K.
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- CR109107
- 75105186CRD1001