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A Clinical Pharmacology Study of ME3208 in Healthy Japanese Male Subjects (Phase 1)

A Clinical Pharmacology Study of ME3208 in Healthy Japanese Male Subjects (Phase 1) - Investigation on the Safety, Tolerability and Pharmacokinetics of ME3208 Single or Multiple Oral Administration, and the Effect of Food on the Pharmacokinetics of ME3208 -

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2071200077
Enrollment
66
Registered
2020-12-25
Start date
2020-12-21
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

chronic graft-versus-host disease

Interventions

Part 1: In cohorts 1-3, ME3208 tablets are administered orally at a single dose of 200, 400, or 800 mg. In the placebo group, placebo tablets are administered. In cohorts 4-6, ME3208 tablets are admin

Sponsors

Kijima Koji
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. Japanese healthy males aged 20 years or over but under 40 years at the time of signing the informed consent 2. Body mass index (BMI) = Body weight (kg) / (Height [m])^2: >=18.5 and <25.0 (at screening) 3. Subjects who exhibited no clinically abnormal findings in the judgment of the investigator or the subinvestigators at screening within 4 weeks before the first dosing, at medical observation, tests, and evaluations on the day before and pre-dose of the first dosing

Exclusion criteria

Exclusion criteria: 1. The subjects had used any medication within 7 days prior to the first dosing (except topical use not intended to systemic activity) 2. The subjects had experienced 400 mL or more of blood collection for donation or other purpose within 12 weeks prior to the first dosing, 200 mL or more of blood within 4 weeks prior to the first dosing, or donation by apheresis within 2 weeks prior to the first dosing 3. The subjects have concurrent or history of cardiac, hepatic, renal, gastrointestinal, respiratory, vascular or hematological function disorders 4. The subjects are positive for urine drug abuse tests 5. The subjects who were judged to be inappropriate to participate in the study by the investigator or the subinvestigators

Design outcomes

Primary

MeasureTime frame
Safety: The safety and tolerability of single or multiple doses for 7 days are assessed by subjective symptoms, objective findings, physiological and clinical examinations. Pharmacokinetics: Part 1: The pharmacokinetics of single or multiple doses for 7 days are investigated by plasma ME3208 and metabolites concentrations, as well as plasma pharmacokinetic parameters. Part 2: The effect of food on the pharmacokinetics of a single dose are investigated by plasma ME3208 and metabolites concentrations, as well as plasma pharmacokinetic parameters.

Contacts

Public ContactClinical Development Dept.

Meiji Seika Pharma Co.,Ltd.

clinical-trials@meiji.com+81-3-3273-3746

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026