ArticleClinical pharmacology and therapeutics2025
Relationship between Dose, Factor IX Activity Levels and Bleeding Probability for rIX-FP Prophylaxis in Hemophilia B: A Repeated Time-to-Event Analysis.
Article in Clinical pharmacology and therapeutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.
What it found
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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.
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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
3 citing papers in PubMed.
- Extended Half-Life Factor Concentrates in Haemophilia Treatment.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2026Review
- Extravascular distribution of factor IX-review of experimental and clinical evidence, and relevance for hemophilia B replacement therapy.Research and practice in thrombosis and haemostasis · 2026Review
- Optimization of hemophilia B treatment via population PK modeling of rIX-FP, including a 3-week regimen.Frontiers in pediatrics · 2025Article
Corrections and comments
- Erratum issued
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
In hemophilia B, pharmacokinetic (PK)-guided dosing of extended half-life factor IX (EHL-FIX) concentrates can secure targeted FIX exposure. Target FIX activity levels in plasma should be individually set primarily taking bleeding tendency into account, alongside the presence of target joints, physical activity, and preferred dosing schedules. In other words, both PK and pharmacodynamics (PD) are relevant when individualizing therapy. Our objective was to examine the relationship between dose, FIX activity levels, and bleeding specifically for EHL-FIX concentrate recombinant fusion protein linking coagulation factor IX with albumin (rIX-FP). Data from hemophilia B patients with endogenous FIX activity level ≤ 2 IU/dL from five clinical trials were combined. Bleeding probability was described with a parametric repeated time-to-event (RTTE) model. Data included 2,493 FIX activity levels and 514 bleeds from 114 unique patients with a median age of 26 years (range: 1-61) followed for a median of 416 days (range: 6-1,233). Joints were the most frequent bleeding site (46%), and more than half of the bleeds were trauma-related (52%). Overall, 60% and 40% were categorized as damage-causing or nuisance bleeds, respectively. A baseline hazard of 7.3 bleeds per year was calculated when FIX activity levels were set at zero. The probability of all bleeding decreased by 50% when the FIX activity level was 12 IU/dL. Variability in bleeding hazard between individuals with similar FIX activity levels was substantial (182%). Simulations showed that targeting trough FIX activity levels to 20 IU/dL resulted in a median annual bleeding rate (ABR) of zero (range: 0-3).
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Registered trials
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