drugset / Trial / NCT03001011

Evaluation of Renvela in Patients With Chronic Kidney Disease Not On Dialysis And Hyperphosphatemia In China

NCT03001011 ↗

Phase 3 Completed 202 enrolled Sanofi
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Primary Objective: To demonstrate efficacy of Renvela tablets in the reduction of serum phosphorus in hyperphosphatemia in participants with chronic kidney disease not on dialysis. Secondary Objectives: To document the efficacy of Renvela tablets in the reduction of serum lipids (total cholesterol and low-density lipoprotein cholesterol \[LDL-C\]). To document the efficacy of Renvela tablets in the reduction of calcium-phosphorus product. To document the efficacy of Renvela tablets in the reduction of intact parathyroid hormone (iPTH). To document the efficacy of Renvela tablets in proportion of participants reaching the target serum phosphorus level 4.6 milligrams per decilitre (mg/dL) (1.47 millimoles per litre \[mmol/L\], inclusive). To evaluate safety of Renvela tablets.

Timeline

Start
2017-06-07
Primary completion
2019-08-16
Completion
2019-08-16

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo vs Renvela; p <0.0001; Median difference (Renvela - Placebo) -0.210 NCT03001011 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Sevelamer Other / unclassified — Oral

Indications