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Record W4413420059 · doi:10.1212/wn9.0000000000000028

Tolebrutinib Phase 2b Long-Term Extension Study

2025· article· en· W4413420059 on OpenAlexaff
Jiwon Oh, Robert J. Fox, Douglas L. Arnold, Sana Syed, Deborah Dukovic, Wendy Vargas, Timothy J. Turner, Conor F. Underwood, Tiha M. Long, Anthony Traboulsee, Daniel S. Reich

Bibliographic record

VenueNeurology Open Access · 2025
Typearticle
Languageen
FieldMedicine
TopicMultiple Sclerosis Research Studies
Canadian institutionsUniversity of British ColumbiaMcGill UniversityNeuroRx Research (Canada)Montreal Neurological Institute and HospitalSt. Michael's Hospital
FundersNational Institutes of Health
KeywordsTerm (time)Extension (predicate logic)Phase (matter)Computer sciencePhysicsProgramming language

Abstract

fetched live from OpenAlex

Background and Objectives: Tolebrutinib is an oral, brain-penetrant, covalent Bruton's tyrosine kinase (BTK) inhibitor currently under investigation as a disease-modifying therapy for multiple sclerosis (MS). In a Phase 2b trial, tolebrutinib administration was generally well tolerated and produced dose-dependent reductions in new gadolinium (Gd)-enhancing T1 and new/enlarging T2 lesions in participants with relapsing MS. We evaluated the safety and effectiveness of tolebrutinib for 2 years after the end of the Phase 2b trial in a long-term safety (LTS) extension study. Methods: This is an ongoing, two-part LTS extension study conducted at academic sites, specialty clinics, and general neurology centers. Participants who completed the Phase 2b trial on treatment were eligible for enrollment. In LTS Part A, participants continued their core study tolebrutinib dose (5, 15, 30, or 60 mg/day) double-blind. In Part B, all participants switched to open-label treatment with the selected Phase 3 dose of tolebrutinib 60 mg/day taken with food. Safety (the primary objective) was measured by adverse events (AEs). Efficacy measures included new Gd-enhancing T1 lesions, new/enlarging T2 lesions, annualized relapse rate (ARR), and Expanded Disability Status Scale (EDSS) score. Results: Of the 129 participants who completed core study treatment, 125 enrolled in LTS Part A and received tolebrutinib, 124 entered Part B, and 114 remain on study as of February 18, 2022. Mean age at core study baseline was 37.8 years and 69% of participants were female. The most common treatment-emergent AEs were COVID-19 (n=26/125, 21%) and headache (n=17/125, 14%). At LTS Week (W)96, 79% of participants assigned in the core study to 60 mg (60 mg/60 mg arm) had no new Gd-enhancing T1 lesions since the previous scan (W72), 33% had no new/enlarging T2 lesions since LTS W0, and 50% had ≤2 new/enlarging T2 lesions since LTS W0. ARR on tolebrutinib 60 mg/day for ≥8 weeks was 0.17 (95% confidence interval: 0.12, 0.25), and median EDSS scores were stable. Discussion: Over 2 years, tolebrutinib showed an acceptable safety profile, with durable effects on MRI measures, ARR, and EDSS. Conclusions regarding efficacy are limited by the study's open-label design and lack of a comparator group. Classification of Evidence: This study provides class IV evidence. It is an uncontrolled study without a comparator group.

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)0.001
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 score0.046
Threshold uncertainty score0.699

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.001
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0000.001
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0010.004
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0010.000

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 head0.183
GPT teacher head0.540
Teacher spread0.357 · 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

Citations4
Published2025
Admission routes1
Has abstractyes

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