MedTrace Logo

Switch and Maintenance Study of Intravenous Injections of R744 to Hemodialysis Patients (Phase Ⅲ Study)

NCT00433888 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 179

Last updated 2009-02-02

No results posted yet for this study

Summary

This study will assess the efficacy and safety of intravenous R744 in renal anemia patients on hemodialysis.

Conditions

  • Hemodialysis Patients

Interventions

DRUG

R744

100μg/4 weeks for 8 weeks,then 25\~400μg/4 weeks for 40 weeks

DRUG

R744

150μg/4 weeks for 8 weeks,then 25\~400μg/4 weeks for 40 weeks

Sponsors & Collaborators

  • Chugai Pharmaceutical

    lead INDUSTRY

Principal Investigators

  • Takanori Baba · Clinical Research Department 2

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-01-31
Primary Completion
2008-07-31
Completion
2008-10-31

Countries

  • Japan

Study Locations

More Related Trials

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 NCT00433888 on ClinicalTrials.gov