Американское общество гирудотерапии

Rebalancing agents in hemophilia: knowns, unknowns, and uncertainties.

Review published in Haematologica (2025)

Последнее обновление: June 18, 2026Рецензент: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Narrative reviewРазработка лекарственных препаратовФармакология секрета слюнных желёзVan Thillo et al. · Haematologica, 2025

Abstract

Treatment options for patients with hemophilia and other bleeding disorders have advanced dramatically over the last few years, not only with the availability of safer factor concentrates, but also with the introduction of factor VIII-mimicking agents. Until recently, there were still areas of hemophilia care that required attention and optimization, including the need for repeated venipuncture, often requiring a central venous access device, and the possible development of inhibitors that limit the efficacy of factor replacement, thereby increasing the complexity and burden of therapy. A new class of rebalancing agents aims to address these remaining issues by inhibiting various natural anticoagulants. Fitusiran is a small interfering RNA agent that reduces antithrombin synthesis in hepatocytes, favoring a procoagulant state. Other promising rebalancing agents are concizumab and marstacimab, which selectively bind to the K2 domain of the tissue factor pathway inhibitor, thus restoring thrombin generation. SerpinPC is a subcutaneous biological inhibitor that blocks the anticoagulant activated protein C pathway, while VGA039 is a monoclonal antibody that targets its cofactor protein S. Although the available clinical data are promising, several important challenges remain. These include the thrombotic risk of rebalancing agents, perioperative and bleeding management, availability in low-income countries, efficacy and factor VIII equivalence compared to existing treatments, ideal target populations, and potential application in other hemostatic disorders. The primary aim of this review is to summarize the best available evidence on these novel rebalancing agents, while highlighting the unknowns, and emphasizing the uncertainties that lie ahead.

Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.

Publication typeJournal ArticleReview
Indexed MeSH termsHumansHemophilia AFactor VIIIAntibodies, Monoclonal, HumanizedDisease Management

Резюме

Treatment options for patients with hemophilia and other bleeding disorders have advanced dramatically over the last few years, not only with the availability of safer factor concentrates, but also with the introduction of factor VIII-mimicking agents. Until recently, there were still areas of...

Почему это важно для гирудотерапии

This review summarizes rebalancing agents for hemophilia and related bleeding disorders, including fitusiran (reducing antithrombin synthesis), concizumab and marstacimab (binding tissue factor pathway inhibitor), SerpinPC (blocking the activated protein C pathway), and VGA039 (targeting protein S), while noting unresolved issues such as thrombotic risk and optimal patient selection. The abstract is relevant to hemostasis and anticoagulant-pathway biology in a hematology context. However, it does not mention leeches, hirudin, leech-derived anticoagulants, or hirudotherapy at any point. Consequently, it provides no direct evidence regarding leech therapy or the leech secretome, and no leech-related relevance should be inferred.

Цитирование

Rebalancing agents in hemophilia: knowns, unknowns, and uncertainties.

Van Thillo et al. · Haematologica, 2025

Связанный клинический контекст

Добавлено в библиотеку ASH: May 28, 2026 · Последнее обновление сайта: June 18, 2026

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