Evidence map›Paper›PMID 31317668›Full record

Trial reportClinical pharmacology in drug development2020

The Pharmacokinetics and Relative Bioavailability of Mepolizumab 100 mg Liquid Formulation Administered Subcutaneously to Healthy Participants: A Randomized Trial.

Shaila Shabbir, Isabelle J Pouliquen, Jane H Bentley, Eric S Bradford, Morrys C Kaisermann, Muna Albayaty

Registry-linked trialOpen access · hybridAbstract readComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in Clinical pharmacology in drug development, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03014674 (An Open Label, Randomised, Three Arm, Single Dose, Multicentre, Parallel Group Study in Healthy Subjects to Compare the Pharmacokinetics of Subcutaneous Mepolizumab When Delivered as a Liquid Drug Product in a Safety Syringe or an Auto Injector With a Reconstituted Lyophilised Drug Product From a Vial), which is not on this map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 17% 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.

NCT03014674 phase3completednot on this map

An Open Label, Randomised, Three Arm, Single Dose, Multicentre, Parallel Group Study in Healthy Subjects to Compare the Pharmacokinetics of Subcutaneous Mepolizumab When Delivered as a Liquid Drug Product in a Safety Syringe or an Auto Injector With a Reconstituted Lyophilised Drug Product From a Vial

TypeinterventionalSponsorGlaxoSmithKlineRan2017 to 2017Enrolled246ConditionsAsthmaArmsLyophilized mepolizumab, Liquid mepolizumab, Prefilled autoinjector, Prefilled Safety Syringe
3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 20 citations in OpenAlex.

  1. Trial
  2. Clinical Qualification of Subcutaneous Injection Devices for Monoclonal Antibodies.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2026
    Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Taking a Breather: Advances in Interleukin 5 Inhibition for Asthma Relief.International journal of molecular sciences · 2022
    Review
  9. 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

6 authors at 5 institutions in 2 countries.

Shaila ShabbirGSK, Gunnels Wood Road, Stevenage, Hertfordshire, UK.
Isabelle J PouliquenGSK, Stockley Park, Uxbridge, Middlesex, UK.
Jane H BentleyGSK, Stockley Park, Uxbridge, Middlesex, UK.
Eric S BradfordGSK, Research Triangle Park, NC, USA.
Morrys C KaisermannGSK, Upper Providence, Collegeville, PA, USA.
Muna AlbayatyPAREXEL International, Northwick Park Hospital, Harrow, Middlesex, UK.
Middlesex University · GBNorth Hertfordshire College · GBPAREXEL International (United Kingdom) · GBProvidence College · USResearch Triangle Park Foundation · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study compared the pharmacokinetic (PK) profile of a new liquid formulation of mepolizumab with the established lyophilized formulation. In this open-label, parallel-group, single-dose study (NCT03014674; GSK ID: 204958), healthy participants were randomized (1:1:1) to receive a single mepolizumab dose (100 mg) administered subcutaneously as liquid in a single-use prefilled syringe or single-use prefilled autoinjector, or as a lyophilized formulation. Maximum plasma concentration, area under the plasma concentration-time curve from time zero (predose) to time of last quantifiable concentration (AUC

Indexed as

AdultAgedAged, 80 and overAnti-Asthmatic AgentsAntibodies, Monoclonal, HumanizedArea Under CurveBiological AvailabilityFemaleFreeze DryingHumansInjections, SubcutaneousMaleMiddle AgedTherapeutic EquivalencyYoung AdultAnti-Asthmatic AgentsAntibodies, Monoclonal, Humanizedmepolizumabasthmabiologicsclinical trialspharmacokinetics and drug metabolismpulmonary

Identifiers

PMID31317668
PMCPMC7187405
OpenAlexW2962798989

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.