Evidence map›Paper›PMID 36093738›Full record

ArticleAnnals of neurology2023

Phase 1 Evaluation of Elezanumab (Anti-Repulsive Guidance Molecule A Monoclonal Antibody) in Healthy and Multiple Sclerosis Participants.

Hari V Kalluri, Matthew R Rosebraugh, Thomas P Misko, Adam Ziemann, Wei Liu, Bruce A C Cree

Registry-linked trialOpen access · hybridAbstract readMulticenter StudyClinical Trial, Phase I
In one paragraph

Article in Annals of neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02601885 (An Escalating Multiple Dose Study of ABT-555 in Subjects With Relapsing Forms of Multiple Sclerosis), which is not on this map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.2field-weighted citation impact, top 7% 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.

NCT02601885 phase1completednot on this map

An Escalating Multiple Dose Study of ABT-555 in Subjects With Relapsing Forms of Multiple Sclerosis

TypeinterventionalSponsorAbbVieRan2016 to 2018Enrolled20ConditionsMultiple SclerosisArmsABT-555, Placebo
3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 23 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. The Present and Future of Monoclonal Antibody Therapies for Multiple Sclerosis.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2025
    Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Intrathecal administration of Anti-Nogo-A antibody in macaque monkeys: Pharmacokinetics, tissue penetration and target interaction.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
    Article
  11. Review
  12. Review
  13. Review
  14. The neuropathobiology of multiple sclerosis.Nature reviews. Neuroscience · 2024
    Review
  15. Article
  16. Review
  17. Review
  18. The State of the Art of Pediatric Multiple Sclerosis.International journal of molecular sciences · 2023
    Review
  19. Review
  20. Review
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

6 authors at 2 institutions in 1 country.

Hari V KalluriClinical Pharmacology and Pharmacometrics, AbbVie, North Chicago, IL.ORCID 0000-0002-5863-2452
Matthew R RosebraughClinical Pharmacology and Pharmacometrics, AbbVie, North Chicago, IL.ORCID 0000-0002-8333-7738
Thomas P MiskoNeuroscience, AbbVie, North Chicago, IL.
Adam ZiemannNeuroscience, AbbVie, North Chicago, IL.
Wei LiuClinical Pharmacology and Pharmacometrics, AbbVie, North Chicago, IL.
Bruce A C CreeWeill Institute of Neurosciences, Department of Neurology, University of California, San Francisco, San Francisco, CA.ORCID 0000-0001-7689-2533
AbbVie (United States) · USUniversity of California, San Francisco · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study was undertaken to describe the safety, tolerability, pharmacokinetics, and immunogenicity of elezanumab (ABT-555), a fully human monoclonal antibody (mAb) directed against repulsive guidance molecule A (RGMa), in healthy and multiple sclerosis (MS) study participants.

methodsThe single-center, first-in-human, single ascending dose (SAD) study evaluated elezanumab (50-1,600mg intravenous [IV] and 150mg subcutaneous) in 47 healthy men and women. The multicenter multiple ascending dose (MAD; NCT02601885) study evaluated elezanumab (150mg, 600mg, and 1,800mg) in 20 adult men and women with MS, receiving either maintenance or no immunomodulatory treatment.

resultsNo pattern of study drug-related adverse events was identified for either the SAD or MAD elezanumab regimens. Across both studies, the T

interpretationThe elezanumab pharmacokinetic profile supports monthly, or bimonthly, administration of up to 1,800mg with the option of a loading dose of 3,600mg. Elezanumab partitioning into CSF is within the range expected for mAbs. Reduced CSF levels of free RGMa demonstrate central nervous system target binding of elezanumab with an apparent maximal effect at 1,800mg IV. Exposure-associated increases in CSF IL-10, an anti-inflammatory cytokine with neuroprotective/neurorestorative properties, support potential pathway modulation in MS participants. ANN NEUROL 2023;93:285-296.

Indexed as

Antibodies, MonoclonalMultiple SclerosisAdministration, IntravenousAdultAntibodies, Monoclonal, HumanizedArea Under CurveDose-Response Relationship, DrugDouble-Blind MethodFemaleHealthy VolunteersHumansInterleukin-10MaleAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedelezanumabInterleukin-10

Identifiers

PMID36093738
PMCPMC10100020
OpenAlexW4295272954

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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 OpenQuestion graph.