Evidence map›Paper›PMID 39158670›Full record

ArticleJournal of clinical immunology2024

Long-Term Safety of Facilitated Subcutaneous Immunoglobulin 10% Treatment in US Clinical Practice in Patients with Primary Immunodeficiency Diseases: Results from a Post-Authorization Safety Study.

Arye Rubinstein, Mohsen Mabudian, Donald McNeil, Niraj C Patel, Richard L Wasserman, Sudhir Gupta, Paz Carrasco, Jie Chen, Enrique Garcia, Andras Nagy and 1 more

Registry-linked trialAbstract readMulticenter Study
In one paragraph

Article in Journal of clinical immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02593188 (Non-Interventional Post-Marketing Safety Study on the Long-Term Safety of HYQVIA), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–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.

NCT02593188 completednot on this map

Non-Interventional Post-Marketing Safety Study on the Long-Term Safety of HYQVIA (Global)

TypeobservationalSponsorBaxalta now part of ShireRan2015 to 2021Enrolled264ConditionsPrimary Immunodeficiency Diseases (PID)ArmsHYQVIA
3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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.

Arye RubinsteinAlbert Einstein College of Medicine and Montefiore Hospital, Bronx, NY, USA.
Mohsen MabudianAllergy Immunology Medical Center, Redlands, CA, USA.
Donald McNeilOptimed Research, Columbus, OH, USA.
Niraj C PatelDuke University, Durham, NC, USA.
Richard L WassermanAllergy Partners of North Texas Research, Dallas, TX, USA.
Sudhir GuptaUniversity of California at Irvine, Irvine, CA, USA.
Paz CarrascoBaxalta Innovations GmbH, a Takeda Company, Vienna, Austria.
Jie ChenTakeda Development Center Americas, Inc., Cambridge, MA, USA.
Enrique GarciaTakeda Development Center Americas, Inc., Cambridge, MA, USA.
Andras NagyBaxalta Innovations GmbH, a Takeda Company, Vienna, Austria. andras.nagy@takeda.com.
Leman Yel *University of California at Irvine, Irvine, CA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Facilitated subcutaneous immunoglobulin (fSCIG) 10% is an immunoglobulin replacement therapy that utilizes recombinant human hyaluronidase (rHuPH20) to enhance immunoglobulin dispersion and absorption, allowing for longer treatment intervals similar to intravenous immunoglobulin (up to once monthly). fSCIG 10% is indicated in the USA for treating adults and children aged ≥ 2 years with primary immunodeficiency diseases (PIDs). This prospective, non-interventional, open-label, multicenter, post-authorization safety study (NCT02593188) was conducted in the USA from November 2015 to October 2021 to assess the long-term safety of fSCIG 10% in routine clinical practice. Patients with PIDs aged ≥ 16 years who were prescribed and/or had started fSCIG 10% treatment were enrolled. In total, 253 patients were enrolled and included (full analysis set). Participants received fSCIG 10% treatment for a median (interquartile range) of 10.0 (3.5-11.8) months, with the majority of infusions administered every 4 weeks (54.4% [1197/2201 infusions]) and at home (62.6% [1395/2230 infusions]). Overall, 98.5% of infusions were administered without rate reduction, interruption, or discontinuation due to adverse events (AEs). Treatment-related, non-serious AEs were experienced by 52 patients (20.6%, 284 events). Two patients (0.8%) each experienced one treatment-related serious AE (aseptic meningitis and deep vein thrombosis). Development of antibodies against rHuPH20 was uncommon; 14/196 patients (7.1%) tested positive for binding antibodies (titer ≥ 1:160) with no neutralizing antibodies detected. There was no relationship between anti-rHuPH20 antibody positivity and the occurrence of treatment-related serious or non-serious AEs. Long-term, repeated self-administration of fSCIG 10% was well tolerated in US clinical practice by patients with PIDs.

Indexed as

HyaluronoglucosaminidaseAdolescentAdultAgedChildChild, PreschoolFemaleHumansImmunoglobulinsImmunologic Deficiency SyndromesInfusions, SubcutaneousInjections, SubcutaneousMaleMiddle AgedPrimary Immunodeficiency DiseasesProspective StudiesHyaluronoglucosaminidaseImmunoglobulinsImmunogenicityImmunoglobulin replacementInborn errors of immunityQuality of lifeTolerability

Identifiers

PMID39158670
PMCPMC11333520

What Socratic holds

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LicenceCC BY
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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 Socratic graph.