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The European medicines agency review of belzutifan (Welireg) for the treatment of adult patients with von Hippel-Lindau disease-associated tumors.

The oncologist 2026 Vol.31(2)

Baron A, Broekman E, van Gils M, Poplavska E, Mol P, Saliete I, Sepodes B, Pean E

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In February 2025, the European Commission granted approval for belzutifan (Welireg) as a treatment for certain von Hippel-Lindau (VHL) disease-associated tumors.

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APA Baron A, Broekman E, et al. (2026). The European medicines agency review of belzutifan (Welireg) for the treatment of adult patients with von Hippel-Lindau disease-associated tumors.. The oncologist, 31(2). https://doi.org/10.1093/oncolo/oyaf433
MLA Baron A, et al.. "The European medicines agency review of belzutifan (Welireg) for the treatment of adult patients with von Hippel-Lindau disease-associated tumors.." The oncologist, vol. 31, no. 2, 2026.
PMID 41507088

Abstract

In February 2025, the European Commission granted approval for belzutifan (Welireg) as a treatment for certain von Hippel-Lindau (VHL) disease-associated tumors. This is the first medicinal product in Europe for pharmacological management of VHL, a rare, hereditary condition characterized by the development of multiple tumors across various organs. Belzutifan is an oral inhibitor of hypoxia-inducible factor-2α (HIF-2α), a protein involved in the pathogenesis of VHL-associated tumors. This approval, which is based on the results of the pivotal phase 2 clinical trial MK-6482-004 (LITESPARK-004) offers a therapeutic approach to managing certain VHL disease-associated tumors. This article describes the clinical data supporting belzutifan approval in the EU, focusing on the VHL disease indication and its mechanism of action.

MeSH Terms

Humans; von Hippel-Lindau Disease; Adult; Europe; Von Hippel-Lindau Tumor Suppressor Protein; Drug Approval; Neoplasms; Indenes