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Bioequivalence study of FKB327 and adalimumab in healthy adult male subjects; Multicenter study

A Phase I, Randomized, Single-Blind, Multicenter, Parallel-Group, Single-Dose Study to Compare Pharmacokinetic Characteristics and Safety of FKB327 with those of Humira in Healthy Adult Male Subjects - FKB327-006 Study

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2071200057
Enrollment
130
Registered
2020-11-25
Start date
2017-07-08
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

Rheumatoid arthritis

Interventions

Sponsors

Yazawa Rie
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: Japanese healthy male subjects aged 20 to 44 years, with body mass index (BMI) of >= 18.5 and < 25.0 kg/m2.

Exclusion criteria

Exclusion criteria: 1. History or presence of illness (including drug or alcohol dependence, drug allergy, allergic disease (including severe natural rubber-latex allergy), respiratory disease, endocrine, renal, or hepatic disease, diabetes mellitus, or cardiac disease) 2. A history of cancer. 3. History or presence of psychiatric disease. 4. Evidence of any significant bacterial, viral, fungal, or parasitic infection within 28 days before dosing. 5. Positive for any one of infectious disease testing (Hepatitis B surface (HBs), anti-HBc antibody, Hepatitis C virus (HCV), Human immunodeficiency virus (HIV) antigen-antibody), and tuberculosis. 6. Positive for any one of drugs of abuse test. 7. History of hepatitis B. 8. Participated in another clinical study or any other type of medical research within 4 months before dosing. 9. Previous treatment with adalimumab. 10. Receipt of a live vaccine (e.g., BCG, polio, measles, rubella) within the 3 months before dosing. 11. History of ADAs to any drug.

Design outcomes

Primary

MeasureTime frame
Pharmacokinetics parameters for bioequivalence: Cmax, AUC0-t

Secondary

MeasureTime frame
Secondary pharmacokinetics parameters: AUC0-infinity, Tmax, T1/2 Safety: Adverse events, Laboratory tests, Vital signs, 12-lead ECG, Anti-drug antibody, Local tolerability, Injection site reaction

Contacts

Public ContactYasumasa Arai

Fujifilm Kyowakirin Biologics Co. Ltd.

yasumasa.arai@fk-b.com+81-3-3282-0700

Outcome results

None listed

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