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Record W4407285619 · doi:10.1093/jcag/gwae059.191

A191 REAL WORLD USE OF ADALIMUMAB BIOSIMILAR AMGEVITA® (ABP-501) IN PATIENTS WITH INFLAMMATORY BOWEL DISEASE IN CANADA

2025· article· en· W4407285619 on OpenAlexaffabout
Muhammad O. Chohan, Rajvi J. Wani, June Copeman, Rina Lukanova, Fatima Dawod, Owen Mooney

Bibliographic record

VenueJournal of the Canadian Association of Gastroenterology · 2025
Typearticle
Languageen
FieldImmunology and Microbiology
TopicBiosimilars and Bioanalytical Methods
Canadian institutionsAmgen (Canada)
Fundersnot available
KeywordsBiosimilarAdalimumabInflammatory bowel diseaseMedicineInflammatory Bowel DiseasesInternal medicineDiseaseGastroenterologyPharmacology

Abstract

fetched live from OpenAlex

Abstract Background ABP-501 (AMGEVITA®), biosimilar to adalimumab reference product (RP), was approved by Health Canada in 2021 for use in different immune diseases, including inflammatory bowel disease (IBD), comprising Crohn’s disease (CD) and ulcerative colitis (UC). Aims To assess the real-world use, effectiveness and satisfaction of ABP-501 in adalimumab naïve and switch patients with IBD across Canada. Methods Data were drawn from the Adelphi IBD Disease Specific ProgrammeTM, a cross-sectional survey with retrospective data collection from physicians conducted in Canada between July 2023 and June 2024. Gastroenterologists (GIs) provided data on their patients with IBD including demographics, clinical characteristics, and treatment satisfaction. Analyses were descriptive. Results Overall, 10 GIs reported data on 101 patients (60 CD and 41 UC): 80 initiated ABP-501 as first adalimumab therapy (initiators) and 21 switched directly to ABP-501 from RP (switchers) (Table 1). Mean [standard deviation; SD] time receiving ABP-501 at consultation was 13.2 [11.6] and 21.6 [9.9] months for initiators and switchers, respectively. Switchers received RP for 48 [27.1] months before switching to ABP-501. Most patients were receiving adalimumab as their first advanced therapy (70% initiators, 90% switchers). The main reasons for switching from RP to ABP-501 were cost effectiveness for the healthcare system (57%) and insurance coverage (43%). At consultation, most initiators and switchers had mild disease (92%, 95%, respectively), were in clinical (91%; 95%, respectively) and endoscopic (66%; 81% respectively) remission (Figure 1) and had an improving/stable disease (97%; 100%, respectively). Treatment targets for initiators and switchers included maintaining clinical remission (n=54; n=18, achieved by 100%, respectively) and maintaining endoscopic remission (n=37; n=17, achieved by 86% and 100%, respectively). GIs were satisfied with ABP-501 treatment (99% initiators, 100% switchers). Conclusions Most patients with IBD treated with ABP-501 as initiating or continuing adalimumab therapy in a real-world setting had mild disease, were in remission and had an improving/stable disease. Patients who switched from RP to ABP-501 switched mainly for economic reasons. GIs reported high levels of satisfaction. Table 1. Demographics and clinical characteristics of patients with IBD receiving ABP-501 at consultation Funding Agencies None

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)0.001
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 score0.449
Threshold uncertainty score0.593

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.000
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 head0.006
GPT teacher head0.205
Teacher spread0.199 · 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".

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Citations0
Published2025
Admission routes2
Has abstractyes

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