Phase 3
Completed N=245
A Phase 3, Randomized, Double Blind, Placebo-Controlled, Multi-Center, Withdrawal Study of MCI-196 in CKD on Dialysis With Hyperphosphatemia
Chronic Kidney Disease · dialysis · Hyperphosphatemia
Source: ClinicalTrials.gov NCT00506441 ↗
Enrolled (actual)
245
Serious AEs
13.0%
Results posted
Jul 2014
Primary outcomePrimary: The Change in Serum Phosphorus From Week 12 to Week 16 — -0.04; 0.71 mg / dL
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, flexible dose titration, the third period is a placebo-controlled withdrawal comparing MCI-196 with placebo for 4 weeks.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY The Change in Serum Phosphorus From Week 12 to Week 16 |
-0.04; 0.71 | — |
| SECONDARY Change From Baseline in Serum Phosphorus |
-1.54 | — |
| SECONDARY Change From Baseline in PTH |
— | — |
| SECONDARY Change From Baseline in Calcium |
— | — |
| SECONDARY Change From Baseline in Calcium x Phosphorus Ion Product |
— | — |
| SECONDARY Change From Baseline in Total Cholesterol |
— | — |
| SECONDARY Change From Baseline in LDL Cholesterol |
— | — |
| SECONDARY Change From Baseline in HDL Cholesterol |
— | — |
| SECONDARY Change From Baseline in VLDL Cholesterol |
— | — |
| SECONDARY Change From Baseline in Triglyceride |
— | — |
| SECONDARY Incidence of Adverse Events |
— | — |
Eligibility Criteria
Inclusion Criteria
- Male or female, and is >=18 years old
- Stable hemodialysis or peritoneal dialysis
- Subjects has Stable phosphate control
- Subjects on Stabilized phosphorus diet
- Subjects undergoing regular dialysis treatment
- Female and of child-bearing potential have a negative serum pregnancy test.
- Male subjects must agree to use appropriate contraception.
Exclusion Criteria
- 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.
- serum albumin level 1000pg/mL
- Hemoglobin level < 8mg/dL
- A History of significant gastrointestinal motility problems
- Biliary obstruction or proven liver dysfunction
- A positive test for hepatitis B surface antigen, hepatitis C antibody or HIV 1 and 2 antibodies
- A clinically significant severe lactose intolerance or sensitivity
- A history of substance or alcohol abuse within the last year.
- Seizure disorders
- A history of drug or other allergy
- using cholestyramine, colestipol or colesevelam
- Schedule to receive a kidney transplant within the next 6 months
- Participation 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
Data sourced from ClinicalTrials.gov (NCT00506441). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.