Evidence map›Paper›PMID 28159782›Full record

Trial reportJournal of the American Society of Nephrology : JASN2017

Effect of Tenapanor on Serum Phosphate in Patients Receiving Hemodialysis.

Geoffrey A Block, David P Rosenbaum, Maria Leonsson-Zachrisson, Magnus Åstrand, Susanne Johansson, Mikael Knutsson, Anna Maria Langkilde, Glenn M Chertow

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of the American Society of Nephrology : JASN, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 3 pooled it
8.9field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

49 citing papers in PubMed, 3 syntheses or guidelines pooled it, 97 citations in OpenAlex.

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  9. The effects of tenapanor on serum fibroblast growth factor 23 in patients receiving hemodialysis with hyperphosphatemia.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2019
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 2 countries.

Geoffrey A BlockDenver Nephrology, Denver, Colorado; gablock@dnresearch.org.
David P RosenbaumArdelyx Inc., Fremont, California.
Maria Leonsson-ZachrissonAstraZeneca Gothenburg, Mölndal, Sweden; and.
Magnus ÅstrandAstraZeneca Gothenburg, Mölndal, Sweden; and.
Susanne JohanssonAstraZeneca Gothenburg, Mölndal, Sweden; and.
Mikael KnutssonAstraZeneca Gothenburg, Mölndal, Sweden; and.
Anna Maria LangkildeAstraZeneca Gothenburg, Mölndal, Sweden; and.
Glenn M ChertowDivision of Nephrology, Stanford University School of Medicine, Stanford, California.
AstraZeneca (Sweden) · SEArdelyx (United States) · USColorado Kidney Care · USStanford University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hyperphosphatemia is common among patients with CKD stage 5D and is associated with morbidity and mortality. Current guidelines recommend lowering serum phosphate concentrations toward normal. Tenapanor is a minimally absorbed small molecule inhibitor of the sodium/hydrogen exchanger isoform 3 that functions in the gut to reduce sodium and phosphate absorption. This randomized, double-blind, placebo-controlled trial assessed the effects of tenapanor on serum phosphate concentration in patients with hyperphosphatemia receiving hemodialysis. After a 1- to 3-week washout of phosphate binders, we randomly assigned 162 eligible patients (serum phosphate =6.0 to <10.0 mg/dl and a 1.5-mg/dl increase from before washout) to one of six tenapanor regimens (3 or 30 mg once daily or 1, 3, 10, or 30 mg twice daily) or placebo for 4 weeks. The primary efficacy end point was change in serum phosphate concentration from baseline (randomization) to end of treatment. In total, 115 patients (71%) completed the study. Mean serum phosphate concentrations at baseline (after washout) were 7.32-7.92 mg/dl for tenapanor groups and 7.87 mg/dl for the placebo group. Tenapanor provided dose-dependent reductions in serum phosphate level from baseline (least squares mean change: tenapanor =0.47-1.98 mg/dl; placebo =0.54 mg/dl;

Indexed as

Renal DialysisAdultAgedAged, 80 and overDouble-Blind MethodFemaleHumansHyperphosphatemiaIsoquinolinesMaleMiddle AgedPhosphatesSulfonamidesIsoquinolinesPhosphatesSulfonamidestenapanorchronic kidney diseasehemodialysishyperphosphatemiaNHE3sodium–hydrogen exchanger 3tenapanor

Identifiers

PMID28159782
PMCPMC5461797
OpenAlexW2584796864

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.