RenaGel®, a nonabsorbed calcium- and aluminum-free phosphate binder, lowers serum phosphorus and parathyroid hormone

Eduardo A. Slatopolsky, Steven K. Burke, Maureen A. Dillon, Paul Bolin, Kenneth Boren, Douglass T. Domoto, Thomas A. Golper, Fred Jones, C. J. Kaupke, Robert Levinson, Michael A. Marx, William Mattern, Mark S. Paller, Maryella D. Sirmon, Randall Stoltz, John Wagner, Marc Weinberg, Barry Wilkes, Duane Wombolt, James Van Gelder

Research output: Contribution to journalArticlepeer-review

275 Scopus citations

Abstract

RenaGel®, a nonabsorbed calcium- and aluminum-free phosphate binder, lowers serum phosphorus and parathyroid hormone. Background. This multicenter, open-label, dose-titration study assessed the safety and efficacy of RenaGelρ, a nonabsorbed calcium-and aluminum-free phosphate binder, in lowering serum phosphorus. Secondary outcomes were its effects on serum intact parathyroid hormone (iPTH) and serum lipids. Methods. Phosphate binders were discontinued during a two-week washout period. Patients whose serum phosphorus was more than 6.0 mg/dl during washout were eligible for treatment. RenaGel®, at starting doses of two, three, or four 440 mg capsules three times per day with meals, was administered to 172 hemodialysis patients for eight weeks. RenaGel® could be increased by one capsule per meal every two weeks as necessary to achieve serum phosphorus control. A second two-week washout period followed. Results. Mean serum phosphorus rose from 6.8 ± 2.0 mg/dl at pre-washout to 9.1 ± 2.4 mg/dl at the end of the washout period. It then declined to 6.6 ± 1.9 mg/dl by the end of the eight- week RenaGel® treatment period (P < 0.0001). Serum phosphorus increased to 8.0± 2.2 mg/dl at the end of the second washout period. The mean dose at the end of RenaGel® treatment was 5.4 g per day. Eighty-four percent of the patients previously used calcium-based phosphate binders. As expected, calcium declined during the initial washout period when calcium-based phosphate binders were discontinued. Mean serum calcium declined from 9.6 ± 1.0 mg/dl at pre-washout to 9.1 ± 0.8 mg/dl after washout. It then increased to 9.4 ± 0.9 mg/dl by the end of RenaGel® treatment. Median serum iPTH increased during the two-week washout from 208 pg/ml to 316 pg/ml and then declined to 224 pg/ml at the end of the eight-week treatment period (P < 0.0001 vs. end of initial washout). After eight weeks of treatment, RenaGel® reduced mean serum total cholesterol from 171.0 ± 43.1 mg/dl to 145.0 ± 38.7 mg/dl (P < 0.0001) and mean serum low-density lipoprotein cholesterol from 102.0 ± 34.9 mg/dl to 75.6 ± 29.4 mg/dl (P < 0.0001). High-density lipoprotein cholesterol, triglycerides, and serum albumin did not change. Conclusions. RenaGel®, a novel and calcium- plus aluminum-free effective phosphate binder, can control serum phosphorus and reduce the levels of PTH and cholesterol without inducing hypercalcemia or other side effects. Thus, this new phosphate binder may be effective in the treatment of renal osteodystrophy in uremic patients.

Original languageEnglish (US)
Pages (from-to)299-307
Number of pages9
JournalKidney international
Volume55
Issue number1
DOIs
StatePublished - 1999

Bibliographical note

Funding Information:
This work was supported by a grant provided by Gel-Tex Pharmaceuticals. We thank Sue Viviano for assistance in the preparation of the manuscript.

Keywords

  • Bone disease
  • Dialysate
  • Hyperphosphatemia
  • Osteodystrophy
  • Renal failure
  • Uremia

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