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March 15, 2026Journal of Inherited Metabolic Disease0 citations

Advances in Therapeutics—Enzyme Replacement Therapy: Long‐Term Evaluation and New Approaches

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RLRobin Lachmann

Key Points

  • To evaluate the long-term effectiveness of enzyme replacement therapies for lysosomal storage disorders and identify areas for improvement.
  • Review of licensed enzyme replacement therapies for various lysosomal storage disorders.
  • Analysis of clinical trial endpoints and real-world effectiveness data.
  • Investigation of second-generation enzyme therapies designed for better cellular penetration.
  • Many existing enzyme replacement therapies show variable effectiveness over long-term use.
  • Significant unmet needs remain for patients treated for years.
  • New therapies aim to enhance clearance from hard-to-reach cells and improve outcomes.

Abstract

The first enzyme replacement therapy (ERT) for a lysosomal storage disorder was marketed more than 30 years ago. We now have licensed products for 12 different conditions, and for a number of conditions, up to three different preparations are commercially available. These products were licensed on the basis of their ability to achieve pre-defined endpoints in clinical trials, but many have now been in clinical use for decades, and large amounts of real-world evidence have been generated. This has shown that not all treatments are equally effective and that there is still much unmet need, even for patients who have been treated for many years. Second-generation enzyme therapies are now being designed that will hopefully lead to improved clearance from currently hard-to-access cells and tissues, hence improving long-term clinical outcomes.

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Cite This Study

Robin Lachmann (2026) studied this question.

synapsesocial.com/papers/69b64c33b42794e3e660d8c9https://doi.org/10.1002/jimd.70166
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