Evidence map›Paper›PMID 30756425›Full record

ArticleBritish journal of clinical pharmacology2019

Bridging adults and paediatrics with secondary hyperparathyroidism receiving haemodialysis: a pharmacokinetic-pharmacodynamic analysis of cinacalcet.

Ping Chen, Winnie Sohn, Adimoolam Narayanan, Per Olsson Gisleskog, Murad Melhem

3 registry-linked trialsOpen access · hybridAbstract read
In one paragraph

Article in British journal of clinical pharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 29% 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.

NCT01290029 phase1completednot on this map

An Open-label, Single-dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Cinacalcet HCl in Pediatric Subjects Aged 28 Days to Less Than 6 Years With Chronic Kidney Disease Receiving Dialysis

TypeinterventionalSponsorAmgenRan2011 to 2015Enrolled14ConditionsChronic Kidney Disease, Hyperparathyroidism, Secondary, Secondary HyperparathyroidismArmsCinacalcet
NCT01439867 phase2terminatednot on this map

An Open-label, Single-arm Study to Assess the Safety & Tolerability of Cinacalcet in Addition to Standard of Care in Pediatric Subjects Age 28 Days to < 6 Yrs With Chronic Kidney Disease & Secondary Hyperparathyroidism Receiving Dialysis

TypeinterventionalSponsorAmgenRan2012 to 2016Enrolled18ConditionsChronic Kidney Disease, Hyperparathyroidism, SecondaryArmsCinacalcet hydrochloride, Standard of Care
NCT02138838 phase3terminatednot on this map

A Randomized, Open-label, Controlled Study to Assess the Efficacy and Safety of Cinacalcet HCl in Pediatric Subjects With Secondary Hyperparathyroidism and Chronic Kidney Disease Receiving Dialysis

TypeinterventionalSponsorAmgenRan2014 to 2016Enrolled55ConditionsChronic Kidney Disease, Secondary HyperparathyroidismArmsCinacalcet HCl, Standard of Care
3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
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

5 authors at 2 institutions in 2 countries.

Ping ChenAmgen Inc., Thousand Oaks, CA, USA.
Winnie SohnAmgen Inc., Thousand Oaks, CA, USA.
Adimoolam NarayananAmgen Inc., Thousand Oaks, CA, USA.
Per Olsson GisleskogSGS Exprimo, London, UK.
Murad MelhemAmgen Inc., Thousand Oaks, CA, USA.
Amgen (United States) · USExpro (United Kingdom) · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsThe aims of this study were to develop a pharmacokinetic (PK) and PK-pharmacodynamic (PK/PD) model of cinacalcet in adults and paediatrics with secondary hyperparathyroidism (SHPT) on dialysis, to test covariates of interest, and to perform simulations to inform dosing in paediatrics with SHPT.

methodsCinacalcet PK, intact parathyroid hormone (iPTH) and corrected calcium (cCa) time courses following multiple daily oral doses (1-300 mg) were modelled using a nonlinear mixed effects modelling approach using data from eight clinical studies. Model-based trial simulations, using adult or paediatric titration schemas, predicted efficacy (iPTH change from baseline and proportion achieving iPTH decrease ≥30%) and safety (cCa change from baseline and proportion achieving cCa ≤8.4 mg/dL) endpoints at 24 weeks.

resultsCinacalcet PK parameters were described by a two-compartment linear model with delayed first-order absorption-elimination (apparent clearance = 287.74 L h

conclusionsModel-based simulations showed that the paediatric cinacalcet starting dose (0.2 mg kg

Indexed as

Models, BiologicalRenal DialysisAdolescentAdultAge FactorsBiomarkersCalcimimetic AgentsChildChild, PreschoolCinacalcetComputer SimulationDrug Dosage CalculationsFemaleHumansHyperparathyroidism, SecondaryHypocalcemiaBiomarkersCalcimimetic AgentsCinacalcetParathyroid HormonePTH protein, humanchronic kidney diseasedialysismodelling and simulationpaediatricsPK/PD

Identifiers

PMID30756425
PMCPMC6533487
OpenAlexW2911898481

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.