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A Bioequivalence Study of enarodustat tablet

Phase I clinical study of enarodustat - Bioequivalence study between new drug product and current drug product - - -

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2071200037
Enrollment
52
Registered
2020-10-05
Start date
2020-10-06
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

Anemia associated with chronic kidney disease

Interventions

A single oral administration of enarodustat current and new drug products, respectively

Sponsors

Koretomo Ryosuke
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. The participant is a healthy Japanese adult male, aged 20 to 45 years, inclusive, at the time of informed consent. 2. BMI of at least 18.5 kg/m2 and less than 25.0 kg/m2

Exclusion criteria

Exclusion criteria: 1. Clinically relevant history or current treatment of serious disease such as cerebral, hepatic, renal, cardiac, pulmonary, gastrointestinal, hematological, endocrine, metabolic or psychiatric disease 2. Found to meet protocol-defined conditions determined by screening results (e.g., laboratory tests, vital sign) 3. History of gestrointestinal surgery that would be expected to influence the absorption of drugs. 4. History or presence of any drug allergy 5. History or presence of drug or alcohol abuse

Design outcomes

Primary

MeasureTime frame
To evaluate the bioequivalence of enarodustat following single dose of oral administration of new drug product and current drug product

Contacts

Public ContactRyosuke Koretomo

Shionogi & Co.,Ltd.

clinicaltrials-info@shionogi.co.jp+81-3-6635-3505

Outcome results

None listed

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