Post-marketing Surveillance of Bixalomer in Patients With Pre-dialysis Chronic Kidney Disease

NCT02805348 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 144

Last updated 2024-10-16

No results posted yet for this study

Summary

The objective of this study is to assess the long-term safety and efficacy of bixalomer under post-marketed setting.

Conditions

Interventions

DRUG

Bixalomer

Oral

Sponsors & Collaborators

  • Astellas Pharma Inc

    lead INDUSTRY

Principal Investigators

  • Central Contact · Astellas Pharma Inc

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-06-01
Primary Completion
2018-12-31
Completion
2018-12-31

Countries

  • Japan

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02805348 on ClinicalTrials.gov