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Record W2912553198 · doi:10.1093/ecco-jcc/jjy222.653

P529 Exposure–response relationship of vedolizumab subcutaneous treatment in patients with ulcerative colitis: VISIBLE 1

2019· article· en· W2912553198 on OpenAlexaff
Maria Rosario, Dan Polhamus, Nathanael L. Dirks, R J Lock, Xinyi Yao, Jingjing Chen, C Chen, Wan Sun, Brian G. Feagan, William J. Sandborn, Geert D’Haens

Bibliographic record

VenueJournal of Crohn s and Colitis · 2019
Typearticle
Languageen
FieldImmunology and Microbiology
TopicBiosimilars and Bioanalytical Methods
Canadian institutionsRobarts Clinical TrialsWestern University
Fundersnot available
KeywordsVedolizumabMedicineUlcerative colitisPlaceboInternal medicineGastroenterologyPharmacokineticsDisease

Abstract

fetched live from OpenAlex

Vedolizumab is a gut-selective, humanised, monoclonal α4β7 integrin antibody approved for intravenous (IV) administration to treat adult patients with moderate–severe ulcerative colitis (UC). The VISIBLE 1 study assessed the efficacy and safety of a novel vedolizumab formulation for subcutaneous (SC) administration in adult patients with moderate–severe UC. We report the exposure–response and immunogenicity results for vedolizumab SC vs. vedolizumab IV. Pharmacokinetic (PK) and exposure–response data for vedolizumab IV are published.1,2 VISIBLE 1 (NCT02611830) was a Phase 3, double-blind, double-dummy, randomised, placebo-controlled trial. After open-label vedolizumab IV induction treatment (300 mg IV at Weeks [Weeks] 0 and 2), patients with a clinical response at WK6 were randomised to maintenance treatment with placebo, vedolizumab 108 mg every 2 weeks SC, or vedolizumab 300 mg every 8 weeks IV. PK serum samples were taken at prespecified time points. Descriptive statistics were used to summarise vedolizumab PK and immunogenicity using a drug-tolerant electrochemiluminescence assay. Vedolizumab trough concentrations (Ctrough) at WK46 (the final comparable trough sample) were grouped by quartiles and clinical outcome rates were calculated. A total of 216 patients were randomised to placebo (n = 56), vedolizumab SC (n = 106), and vedolizumab IV (n = 54). Both higher vedolizumab SC Ctrough and vedolizumab IV Ctrough concentrations were associated with greater efficacy at WK52, with improved response for low-exposure patients in the SC arm. An increase in WK52 clinical remission was observed in both arms, from 50% to 83% of patients in SC and from 18% to 90% in IV. An increase in WK52 mucosal healing was observed in 50% to 89% of patients in SC and 27% to 100% of patients in IV. A similar trend was observed for both predicted steady-state average concentration and troughs. WK52 exposure–response results for vedolizumab IV were generally comparable with GEMINI 1 results. [1] Immunogenicity was similar for vedolizumab SC and IV and was not associated with injection-site or hypersensitivity reactions. Exposure–response relationships in VISIBLE 1 were similar to those seen previously in GEMINI 1.1,2 Higher serum concentrations of vedolizumab with SC and IV administration during maintenance therapy are associated with greater proportions of patients achieving clinical remission and mucosal healing. Figure 1. Week 52 vedolizumab SC efficacy according to Ctrough quartiles. References 1. Rosario M, Dirks NL, Milch C, et al. A review of the clinical pharmacokinetics, pharmacodynamics, and immunogenicity of vedolizumab. Clin Pharmacokinet 2017;56:1287-1301. 2. Feagan BG, Rutgeerts P, Sands BE et al. Vedolizumab as induction and maintenance therapy for ulcerative colitis. N Engl J Med 2013;369:699–710.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.218
Threshold uncertainty score0.351

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.012
GPT teacher head0.257
Teacher spread0.245 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations5
Published2019
Admission routes1
Has abstractyes

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