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Novel drugs approved by the EMA, the FDA and the MHRA in 2025: A year in review

  • Andreas Papapetropoulos*
  • , Stavros Topouzis*
  • , Steve P H Alexander
  • , Miriam M Cortese-Krott
  • , Zsuzsanna Helyes
  • , Kirill Martemyanov
  • , Claudio Mauro
  • , Nithyanandan Nagercoil
  • , Reynold A Panettieri
  • , Hemal H Patel
  • , Rainer Schulz
  • , Barbara Stefanska
  • , Gary J Stephens
  • , Nathalie Vergnolle
  • , Xin Wang
  • , Stephen Ward
  • , Péter Ferdinandy*
  • *Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

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Abstract

In the 2025 novel drug mini-review, one can take a full measure of the ingenuity that underlies current drug design and development, despite the year's smaller harvest (46 novel drugs) compared to 2024 (53) and 2023 (70). 54% of the novel drugs are first-in-class (FIC). The emphasis on proteins/antibodies is maintained (~25% novel drugs in 2025), an industry trend that does not seem to abate. Fewer than half of the novel medicines address major or common disorders. Among the FIC drugs, it is worth mentioning the Na v1.8 channel inhibitor suzetrigine, the first non-opioid approved to palliate acute pain; the first positive allosteric modulator of transient receptor potential melastatin 8 (TRPM8), acoltremon, that increases basal tear production in dry eye disease, a globally common disorder; lerodalcibep, a 'third generation' adnectin inhibitor of the protease Proprotein Convertase Subtilisin/Kexin type 9 (PCSK9) to treat elevated LDL-c; and zoliflodacin and gepotidacin, both innovatively targeting bacterial topoisomerases to treat uncomplicated urinary tract infections. Most of the approved medicines target unmet medical need areas and/or orphan indications (the latter alone accounting for 41% of the 2025 novel drugs) by applying imaginative approaches. These approaches include: the combination of two FIC drugs, the RAF/MEK clamp avutometinib paired with the FAK/Pyk2 inhibitor defactinib, to block more efficiently the RAS-RAF-MEK-ERK/FAK oncogenic pathway in low-grade serous ovarian cancer; fitusiran, the first RNAi therapy for haemophilia, targeting for the first time the production of the natural anticoagulant anti-thrombin in the liver; and brensocatib, which attenuates the activation of downstream neutrophil proteases by inhibiting the protease DPP1, thereby preventing lung tissue destruction in bronchiectasis. The landscape of novel drugs approved in 2025 reveals that pharmaceutical innovation continues to advance through FIC mechanisms, sophisticated therapeutic approaches, and a strong focus on unmet medical need.

Original languageEnglish
Number of pages35
JournalBritish Journal of Pharmacology
Early online date2 Mar 2026
DOIs
Publication statusE-pub ahead of print - 2 Mar 2026

Bibliographical note

© 2026 The Author(s). British Journal of Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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