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Biosimilar switch for fabry disease shows promise in small trial

NCT ID NCT05843916

First seen Feb 25, 2026 · Last updated May 22, 2026 · Updated 14 times

Summary

This study tested whether a new, similar version of the drug agalsidase beta (called AGA BETA BS) works as well as the standard drug Fabrazyme in people with Fabry disease. Twenty adults who were already stable on Fabrazyme switched to the new drug for 6 months to a year. The main goal was to check if a key disease marker in the blood stayed the same, showing the new drug is equally effective.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Locations

  • Centro Médico Santa María de la Salud

    San Isidro, Buenos Aires, 1642, Argentina

  • Centro Oncológico Riojano Integral

    La Rioja, F5300, Argentina

  • Clínica Universitaria Reina Fabiola

    Córdoba, X5004, Argentina

  • Instituto de Investigaciones Clínicas Quilmes

    Buenos Aires, Argentina

  • Instituto de Nefrología Pergamino S.R.L

    Pergamino, Buenos Aires, 2700, Argentina

Conditions

Explore the condition pages connected to this study.