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A Long-term Study of JR-131 in Renal Anemia Patients With Chronic Kidney Disease (CKD)

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02912533
Enrollment
Unknown
Registered
2016-09-23
Start date
2016-09-30
Completion date
2018-03-31
Last updated
2019-04-02

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

Conditions

Anemia

Brief summary

The purpose of this study is to investigate the safety and efficacy for 52-week dosing of JR-131 in renal anemia patients with chronic kidney disease (CKD).

Interventions

DRUGJR-131

Sponsors

JCR Pharmaceuticals Co., Ltd.
CollaboratorINDUSTRY
Kissei Pharmaceutical Co., Ltd.
Lead SponsorINDUSTRY

Study design

Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum

Inclusion criteria

* Patients being treated with erythropoiesis stimulating agent.

Exclusion criteria

* Patients having complication or history of a cardiovascular / lung / brain infarction. * Patients having a pronounced hemorrhagic lesion.

Design outcomes

Primary

MeasureTime frame
Measure adverse events52 weeks

Secondary

MeasureTime frame
Hemoglobin level52 weeks

Countries

Japan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026