Evidence map›Paper›PMID 39380259›Full record

ArticleCPT: pharmacometrics & systems pharmacology2024

Immunogenicity dynamics and covariate effects after satralizumab administration predicted with a hidden Markov model.

Rory Leisegang, Hanna E Silber Baumann, Siân Lennon-Chrimes, Hajime Ito, Kazuhiro Miya, Jean-Christophe Genin, Elodie L Plan

2 registry-linked trialsAbstract read
In one paragraph

Article in CPT: pharmacometrics & systems pharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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.

NCT02028884 phase3completednot on this map

A Multicenter, Randomized, Addition to Baseline Treatment, Double-Blind, Placebo-Controlled, Phase 3 Study to Evaluate the Efficacy and Safety of Satralizumab (SA237) in Patients With Neuromyelitis Optica (NMO) and NMO Spectrum Disorder (NMOSD)

TypeinterventionalSponsorHoffmann-La RocheRan2014 to 2021Enrolled85ConditionsNeuromyelitis Optica (NMO), NMO Spectrum Disorder (NMOSD)ArmsSatralizumab, Placebo, Baseline Treatment
NCT02073279 phase3completednot on this map

A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Evaluate the Efficacy and Safety of Satralizumab (SA237) as Monotherapy in Patients With Neuromyelitis Optica (NMO) and Neuromyelitis Optica Spectrum Disorder (NMOSD)

TypeinterventionalSponsorHoffmann-La RocheRan2014 to 2022Enrolled95ConditionsNeuromyelitis Optica (NMO), NMO Spectrum Disorder (NMOSD)ArmsSatralizumab, Placebo
3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

7 authors.

Rory LeisegangDepartment of Pharmacy, Uppsala University, Uppsala, Sweden.ORCID 0000-0003-0810-4771
Hanna E Silber BaumannRoche Pharma Research and Early Development, Pharmaceutical Sciences, Roche Innovation Center Basel, Basel, Switzerland.ORCID 0000-0003-4928-6284
Siân Lennon-ChrimesRoche Products Ltd, Welwyn, UK.ORCID 0000-0002-2287-3406
Hajime ItoChugai Pharmaceutical Co., Tokyo, Japan.ORCID 0009-0007-9882-2668
Kazuhiro MiyaChugai Pharmaceutical Co., Tokyo, Japan.ORCID 0009-0001-2309-5642
Jean-Christophe GeninRoche Pharma Research and Early Development, Pharmaceutical Sciences, Roche Innovation Center Basel, Basel, Switzerland.ORCID 0009-0000-9908-5697
Elodie L PlanDepartment of Pharmacy, Uppsala University, Uppsala, Sweden.ORCID 0000-0002-2255-3904

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunogenicity is the propensity of a therapeutic protein to generate an immune response to itself. While reporting of antidrug antibodies (ADAs) is increasing, model-based analysis of such data is seldom performed. Model-based characterization of factors affecting the emergence and dissipation of ADAs may inform drug development and/or improve understanding in clinical practice. This analysis aimed to predict ADA dynamics, including the potential influence of individual covariates, following subcutaneous satralizumab administration. Satralizumab is a humanized IgG2 monoclonal recycling IL-6 receptor antagonist antibody approved for treating neuromyelitis optica spectrum disorder (NMOSD). Longitudinal pharmacokinetic (PK) and ADA data from 154 NMOSD patients in two pivotal Phase 3 studies (NCT02028884, NCT02073279) and PK data from one Phase 1 study (SA-001JP) in 72 healthy volunteers were available for this analysis. An existing population PK model was adapted to derive steady-state concentration without ADA for each patient. A mixed hidden Markov model (mHMM) was developed whereby three different states were identified: one absorbing Markov state for non-ADA developer, and two dynamic and inter-connected Markov states-transient ADA negative and positive. Satralizumab exposure and body mass index impacted transition probabilities and, therefore, the likelihood of developing ADAs. In conclusion, the mHMM model was able to describe the time course of ADA development and identify patterns of ADA development in NMOSD patients following treatment with satralizumab, which may allow for the formulation of strategies to reduce the emergence or limit the impact of ADA in the clinical setting.

Indexed as

Markov ChainsNeuromyelitis OpticaAdultAgedAntibodies, Monoclonal, HumanizedClinical Trials, Phase III as TopicFemaleHumansLongitudinal StudiesMaleMiddle AgedModels, BiologicalYoung AdultAntibodies, Monoclonal, Humanized

Identifiers

PMID39380259
PMCPMC11646947

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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.