Normal immunoglobulin human 10g/100ml solution for infusion vials and Recombinant human hyaluronidase solution for infusion 5ml vials
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Data from the MHRA Yellow Card scheme. A reported reaction does not necessarily mean the medicine caused it. Contains public sector information licensed under the Open Government Licence v3.0.
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1 branded products available
Part of the Sandoglobulin brand family (generic: Normal immunoglobulin human)
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View all licensed products for Normal immunoglobulin human on the MHRA register
HyQvia 10g/100ml solution for infusion and 5ml vials
Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
NHS prescribing volume and spending trends
Guidelines from the National Institute for Health and Care Excellence
NICE clinical guidance(5)
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Source: National Institute for Health and Care Excellence (NICE). Contains public sector information licensed under the Open Government Licence v3.0.
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SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. BNF code shown is the factual mapping value distributed by NHS Business Services Authority (NHSBSA) in the dm+d supplementary file under OGL v3.0; it is not affiliated with, nor licensed from, the publishers of the British National Formulary. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 2 · Randomised trials: 1 · 1965–2026
Showing the 50 most relevant studies, sorted by most relevant.
Jian Gao, Q. Zheng, Na Xin, et al.
Cancer Science, 2017
Michael A. Caligiuri
Blood, 2008
- Cytotoxicity, Immunologic
- Immunologic Surveillance
- Interferon-gamma
Allyson L. Byrd, Yasmine Belkaid, Julia A. Segre
Nature Reviews Microbiology, 2018
- Microbiota
- Bacteria
- Skin
Paulina Markowiak‐Kopeć, Katarzyna Śliżewska
Nutrients, 2017
- Gastrointestinal Microbiome
- Clinical Trials as Topic
- Diet
Ayuko Hoshino, Han Sang Kim, Linda Bojmar, et al.
Cell, 2020
- Extracellular Vesicles
- Machine Learning
- Cell Line
Giampaolo Merlini, Angela Dispenzieri, Vaishali Sanchorawala, et al.
Nature Reviews Disease Primers, 2018
- Immunoglobulin Light-chain Amyloidosis
- Angiotensin-Converting Enzyme Inhibitors
- Anti-Bacterial Agents
Haoyu Sun, Qiang Huang, Meijuan Huang, et al.
Hepatology, 2019
M. Khodadoust, N. Olsson, Lisa E. Wagar, et al.
Nature, 2017
Azar AE, Sleasman JW, Steeland S, et al.
2026
- Streptococcus pneumoniae
- Pneumococcal Vaccines
- Immunity, Humoral
Background/objectiveEfgartigimod, a human immunoglobulin G1 (IgG1) antibody Fc fragment, reduces IgG levels through neonatal Fc receptor (FcRn) blockade. Preliminary observational data suggest that efgartigimod does not impair vaccine-induced T cell-dependent antibody responses. The objective of this study was to further evaluate the effect of efgartigimod on T cell-independent humoral immune response to immunization with a 23-valent polysaccharide pneumococcal vaccine (PPSV23).MethodsIn this Phase 1 open-label study, healthy adults (N=37) were randomized 1:1:1 into 3 cohorts: EFG-1 (n=12), EFG-2 (n=12), and placebo (n=13). Four weekly efgartigimod (10 mg/kg intravenously) or placebo infusions were administered with a 6-week follow-up. PPSV23 was administered immediately before (EFG-1/placebo) or 2 weeks after (EFG-2) the last efgartigimod or placebo infusion. The primary endpoint was change in pneumococcal capsular polysaccharide titers after PPSV23 vaccination. Additional endpoints included opsonizing antibody titers, antigen-specific B cell responses, and safety.ResultsAlthough variability in antibody response was observed for individual participants and serotypes, an increase in IgG levels was observed for all 23 pneumococcal serotypes after vaccination, irrespective of efgartigimod timing. Normal response to vaccination (≥2-fold increase and >1.3 mg/L for ≥70% of serotypes) was observed in 90.0% (9 of 10) of the EFG-1 group, 54.5% (6 of 11) of the EFG-2 group, and 33.3% (4 of 12) of the placebo group. Efgartigimod did not impair production of opsonizing antibodies or antigen-specific plasma B cells. No serious/severe adverse events occurred.ConclusionsResults of this exploratory study suggest that efgartigimod has no apparent effect on T cell-independent humoral immune responses to PPSV23 vaccine in healthy adults. Participants in all groups were able to mount antigen-specific IgG responses to vaccination, even when vaccination occurred at the time of maximal reduction in total IgG.Clinical trial registrationhttps://clinicaltrials.gov/study/NCT05163834, identifier NCT05163834.
Abstract licence: CC BY
Jacques M. Lemire, John S. Adams, Rebecca Sakai, et al.
Journal of Clinical Investigation, 1984
- Mitogens
- Calcitriol
- Cell Division
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
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Linked open data from Wikidata (Q57266522), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication.
Scientific data (pharmacology, interactions, ADME) is not yet available for this medicine. Clinical sections are sourced from the NHS dm+d database.