Evidence map›Paper›PMID 42399762›Full record

ArticleBMC nephrology2026

Complement inhibitor therapy in atypical hemolytic uremic syndrome (aHUS): evaluating the economic impact of introducing eculizumab biosimilars in Germany.

Isabell Kaufhold, Daniel Lewkowicz, Danila Seidel, Paul Thomas Brinkkoetter, Florian Kron

Abstract read
In one paragraph

Article in BMC nephrology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Isabell KaufholdVITIS Healthcare Group, Cologne, Germany.
Daniel LewkowiczVITIS Healthcare Group, Cologne, Germany.
Danila SeidelVITIS Healthcare Group, Cologne, Germany.
Paul Thomas BrinkkoetterDepartment II of Internal Medicine, Center for Molecular Medicine Cologne, Faculty of Medicine, University Hospital of Cologne, University of Cologne, Cologne, Germany.
Florian KronVITIS Healthcare Group, Cologne, Germany. florian.kron@fom.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEculizumab, a humanized monoclonal antibody, inhibits activation of complement component C5. For patients with atypical hemolytic uremic syndrome, the introduction of eculizumab has markedly improved survival, restoring life expectancy close to that of the general population. The long-acting C5 complement inhibitor (CI) ravulizumab has since expanded treatment options, offering extended dosing intervals. In 2023, the first eculizumab biosimilars received market authorization. This study aims to evaluate the short-term economic impact of CIs from a German healthcare payer perspective.

methodsAn economic model with weekly cycles and a time horizon of one year was developed to assess treatment costs for eculizumab originator, eculizumab biosimilars, and ravulizumab in adult patients with atypical hemolytic uremic syndrome, based on a standard adult body weight of 77.7 kg. The analysis included direct drug acquisition costs calculated on a milligram basis, obtained from publicly available German price databases and outpatient reimbursement regulations, as well as preparation costs for infusions. Treatment costs were analyzed up to 52 weeks to reflect short-term and annual treatment periods. All costs are presented in euros (2025), and no discounting was performed.

resultsMilligram-based prices were estimated at €12.92 for eculizumab biosimilar, €17.87 for eculizumab originator, and €13.63 for ravulizumab. After 13 weeks, cumulative costs were €124,941 (biosimilar), €172,466 (originator), and €127,062 (ravulizumab). After 52 weeks, costs reached €421,439, €581,836, and €352,463, respectively.

conclusionsAt treatment initiation, the eculizumab biosimilar appears to be the most cost-efficient option among CIs in Germany, offering cost savings relative to both the originator and the long-acting agent. Sequential use of different CIs may therefore represent a cost-saving option.

Indexed as

Antibodies, Monoclonal, HumanizedAtypical Hemolytic Uremic SyndromeBiosimilar PharmaceuticalsComplement Inactivating AgentsCost-Benefit AnalysisDrug CostsGermanyHumansModels, EconomicAntibodies, Monoclonal, HumanizedBiosimilar PharmaceuticalsComplement Inactivating AgentseculizumabravulizumabAtypical hemolytic uremic syndromeBiosimilarsCost-minimization analysisEculizumabRavulizumab

Identifiers

PMID42399762
PMCPMC13340090

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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.