Status:
COMPLETED
A Phase III, Multicentre, Double-Blind, Placebo-Controlled Withdrawal Study in Patients With Hyperphosphatemia
Lead Sponsor:
Tanabe Pharma Corporation
Conditions:
Chronic Kidney Disease
Hyperphosphatemia
Eligibility:
All Genders
18+ years
Phase:
PHASE3
Brief Summary
This is a phase III multi-centre study in three periods: the first period is a phosphate binder washout for 4 weeks, the second period is an open-label, randomised, parallel group, flexible dose, the ...
Eligibility Criteria
Inclusion
- Male or female, 18 years of age or over
- Clinically stable haemodialysis or peritoneal dialysis
- Stable phosphate control
- On a stabilised phosphorus diet
- Female and of child-bearing potential have a negative serum pregnancy test.
- Male subjects must agree to use appropriate contraception.
Exclusion
- Current clinically significant medical comorbidities, which may substantially compromise subject safety, or expose them to undue risk, or interfere significantly with study procedures and which, in the opinion of the Investigator, makes the subject unsuitable for inclusion in the study.
- Body Mass Index (BMI) \<=16.0 kg/m2 or \>=40.0 kg/m2
- A current or history of significant gastrointestinal motility problems
- A positive test for HIV 1 and 2 antibodies
- A history of substance or alcohol abuse within the last year.
- Seizure disorders
- A history of drug or other allergy
- A temporary catheter as a vascular access
- Participated in a clinical study with any experimental medication in the last 30 days or an experimental biological product within the last 90 days prior to signing of informed consent
Key Trial Info
Start Date :
June 1 2007
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 1 2009
Estimated Enrollment :
336 Patients enrolled
Trial Details
Trial ID
NCT00416520
Start Date
June 1 2007
End Date
November 1 2009
Last Update
January 8 2026
Active Locations (68)
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1
Adelaide, Australia
2
Nedlands, Australia
3
Parkville, Australia
4
St Leonards, Australia