Evidence map›Paper›PMID 28711959›Full record

ArticleJournal of clinical immunology2017

A Multicentre Study on the Efficacy, Safety and Pharmacokinetics of IqYmune®, a Highly Purified 10% Liquid Intravenous Immunoglobulin, in Patients with Primary Immune Deficiency.

Gergely Krivan, Ludmila Chernyshova, Larysa Kostyuchenko, Andrzej Lange, Zoltan Nyul, Beata Derfalvi, Jacek Musial, Anne Bellon, Martin Kappler, Alain Sadoun and 1 more

Abstract readEvaluation StudyMulticenter Study
In one paragraph

Article in Journal of clinical immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Trial
  7. fSCIG 10% in pediatric primary immunodeficiency diseases: a European post-authorization safety study.Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology · 2024
    Article
  8. 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

11 authors.

Gergely KrivanPaediatric Haematology and Stem Cell Transplantation Department, Szent Laszlo Hospital, Budapest, Hungary.
Ludmila ChernyshovaDepartment of Paediatric Infectious Diseases and Clinical Immunology, P.L. Shupyk National Medical Academy for Post-graduate Education, Kiev, Ukraine.
Larysa KostyuchenkoWest Ukrainian Specialized Children's Medical Centre, Lviv, Ukraine.
Andrzej LangeLower Silesian Center for Cellular Transplantation/Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wroclaw, Poland.
Zoltan NyulChildren's Department, University of Pécs, Pécs, Hungary.
Beata Derfalvi2nd Department of Paediatrics, Semmelweis University, Budapest, Hungary.
Jacek MusialAlergiczno Internistyczny All-Med Specjalistyczny Osrodek, Krakow, Poland.
Anne BellonClinical Development Department, LFB Biotechnologies, BP 40305, 3 avenue des Tropiques, Les Ulis, 91958, Courtaboeuf Cedex, France.
Martin KapplerStatalpha, Baziège, France.
Alain SadounClinical Development Department, LFB Biotechnologies, BP 40305, 3 avenue des Tropiques, Les Ulis, 91958, Courtaboeuf Cedex, France. sadoun@lfb.fr.
Ewa BernatowskaImmunology Clinic Department, Children's Memorial Health Institute, Warsaw, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This multicentre, open-label, prospective, single-arm study was designed to evaluate the efficacy, pharmacokinetics, and safety of IqYmune®, a highly purified 10% polyvalent immunoglobulin preparation for intravenous administration in patients with primary immunodeficiency. IqYmune® was administered to 62 patients (aged 2-61 years) with X-linked agammaglobulinemia or common variable immune deficiency at a dose from 0.22 to 0.97 g/kg every 3 to 4 weeks for 12 months with an infusion rate up to 8 mL/kg/h. A pharmacokinetic study was performed at steady state between the 8th and the 9th infusion. A single case of serious bacterial infection was observed, leading to an annualized rate of serious bacterial infections/patient (primary endpoint) of 0.017 (98% CI: 0.000, 0.115). Overall, 228 infections were reported, most frequently bronchitis, chronic sinusitis, nasopharyngitis and upper respiratory tract infection. The mean annualized rate of infections was 3.79/patient. A lower risk of infections was associated with an IgG trough level > 8 g/L (p = 0.01). The mean annualized durations of absence from work or school and of hospitalization due to infections were 1.01 and 0.89 days/patient, respectively. The mean serum IgG trough level before the 6th infusion was 7.73 g/L after a mean dose of IqYmune® of 0.57 g/kg. The pharmacokinetic profile of IqYmune® was consistent with that of other intravenous immunoglobulins. Overall, 15.5% of infusions were associated with an adverse event occurring within 72 h post infusion. Headache was the most common adverse event. In conclusion, IqYmune® was shown to be effective and well tolerated in patients with primary immunodeficiency.

Indexed as

AdolescentAdultAgammaglobulinemiaChildChild, PreschoolClinical Trials as TopicCommon Variable ImmunodeficiencyDrug-Related Side Effects and Adverse ReactionsEuropeFemaleGenetic Diseases, X-LinkedHeadacheHumansImmunoglobulins, IntravenousImmunotherapyMaleImmunoglobulins, IntravenousClinical trialsImmunoglobulinsIVIg

Identifiers

PMID28711959
PMCPMC5554475

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Registered trials

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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.