Evidence map›Paper›PMID 33015643›Full record

ArticleThe Lancet. Rheumatology2020

Anti-C5a antibody IFX-1 (vilobelimab) treatment versus best supportive care for patients with severe COVID-19 (PANAMO): an exploratory, open-label, phase 2 randomised controlled trial.

Alexander P J Vlaar, Sanne de Bruin, Matthias Busch, Sjoerd A M E G Timmermans, Ingeborg E van Zeggeren, Rutger Koning, Liora Ter Horst, Esther B Bulle, Frank E H P van Baarle, Marcel C G van de Poll and 16 more

Open access · bronzeAbstract read
In one paragraph

Article in The Lancet. Rheumatology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 121 papers, 10 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
121citing papers in PubMed, 10 pooled it
4.1field-weighted citation impact, top 4% 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.

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

121 citing papers in PubMed, 10 syntheses or guidelines pooled it, 199 citations in OpenAlex.

  1. 2025 Clinical Practice Guideline Update by the Infectious Diseases Society of America on the Treatment and Management of COVID-19: Vilobelimab.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2026
    Guideline
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61 more citing papers are in PubMed but not listed here.

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

26 authors at 6 institutions in 2 countries.

Alexander P J VlaarDepartment of Intensive Care, University of Amsterdam, Amsterdam UMC, Amsterdam, Netherlands.
Sanne de BruinDepartment of Intensive Care, University of Amsterdam, Amsterdam UMC, Amsterdam, Netherlands.
Matthias BuschDepartment of Immunology, Maastricht UMC, Maastricht, Netherlands.
Sjoerd A M E G TimmermansDepartment of Immunology, Maastricht UMC, Maastricht, Netherlands.
Ingeborg E van ZeggerenDepartment of Neurology, Amsterdam Neuroscience, University of Amsterdam, Amsterdam UMC, Amsterdam, Netherlands.
Rutger KoningDepartment of Neurology, Amsterdam Neuroscience, University of Amsterdam, Amsterdam UMC, Amsterdam, Netherlands.
Liora Ter HorstDepartment of Neurology, Amsterdam Neuroscience, University of Amsterdam, Amsterdam UMC, Amsterdam, Netherlands.
Esther B BulleDepartment of Intensive Care, University of Amsterdam, Amsterdam UMC, Amsterdam, Netherlands.
Frank E H P van BaarleDepartment of Intensive Care, University of Amsterdam, Amsterdam UMC, Amsterdam, Netherlands.
Marcel C G van de PollDepartment of Intensive Care, Maastricht UMC, Maastricht, Netherlands.
E Marleen KemperClinical Pharmacy, University of Amsterdam, Amsterdam UMC, Amsterdam, Netherlands.
Iwan C C van der HorstDepartment of Intensive Care, Maastricht UMC, Maastricht, Netherlands.
Marcus J SchultzDepartment of Intensive Care, University of Amsterdam, Amsterdam UMC, Amsterdam, Netherlands.
Janneke HornDepartment of Intensive Care, University of Amsterdam, Amsterdam UMC, Amsterdam, Netherlands.
Frederique PaulusDepartment of Intensive Care, University of Amsterdam, Amsterdam UMC, Amsterdam, Netherlands.
Lieuwe D BosDepartment of Intensive Care, University of Amsterdam, Amsterdam UMC, Amsterdam, Netherlands.
W Joost WiersingaDepartment of Infectious Diseases, University of Amsterdam, Amsterdam UMC, Amsterdam, Netherlands.
Martin WitzenrathDepartment of Infectious Diseases and Respiratory Medicine, Division of Pulmonary Inflammation, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Simon RueckingerMetronomia Clinical Research, Munich, Germany.
Korinna PilzInflaRx, Jena, Germany.
Matthijs C BrouwerDepartment of Neurology, Amsterdam Neuroscience, University of Amsterdam, Amsterdam UMC, Amsterdam, Netherlands.
Ren-Feng GuoInflaRx Pharmaceuticals, Ann Arbor, MI, USA.
Leo HeunksDepartment of Intensive Care, Free University, Amsterdam UMC, Amsterdam, Netherlands.
Pieter van PaassenDepartment of Immunology, Maastricht UMC, Maastricht, Netherlands.
Niels C RiedemannInflaRx, Jena, Germany.
Diederik van de BeekDepartment of Neurology, Amsterdam Neuroscience, University of Amsterdam, Amsterdam UMC, Amsterdam, Netherlands.
University of Amsterdam · NLAmsterdam University Medical Centers · NLMaastricht University Medical Centre · NLInflarx (Germany) · DEAmsterdam Neuroscience · NLCharité - Universitätsmedizin Berlin · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSevere COVID-19 is characterised by inflammation and coagulation in the presence of complement system activation. We aimed to explore the potential benefit and safety of selectively blocking the anaphylatoxin and complement protein C5a with the monoclonal antibody IFX-1 (vilobelimab), in patients with severe COVID-19.

methodsWe did an exploratory, open-label, randomised phase 2 trial (part of the adaptive phase 2/3 PANAMO trial) of intravenous IFX-1 in adults with severe COVID-19 at three academic hospitals in the Netherlands. Eligibility criteria were age 18 years or older; severe pneumonia with pulmonary infiltrates consistent with pneumonia, a clinical history of severe shortness of breath within the past 14 days, or a need for non-invasive or invasive ventilation; severe disease defined as a ratio of partial pressure of arterial oxygen to fractional concentration of oxygen in inspired air (PaO

findingsBetween March 31 and April 24, 2020, 30 patients were enrolled and randomly assigned to the IFX-1 group (n=15) or the control group (n=15). During the study it became clear that several patients could not be assessed regularly in the supine position because of severe hypoxaemia. It was therefore decided to focus on all PaO

interpretationIn this small exploratory phase 2 part of the PANAMO trial, C5a inhibition with IFX-1 appears to be safe in patients with severe COVID-19. The secondary outcome results in favour of IFX-1 are preliminary because the study was not powered on these endpoints, but they support the investigation of C5a inhibition with IFX-1 in a phase 3 trial using 28-day mortality as the primary endpoint.

fundingInflaRx.

Identifiers

PMID33015643
PMCPMC7521913
OpenAlexW3088243710

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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.