AMT-130 gene therapy: a promising disease-modifying approach for Huntington's disease

Chisanga Mwape1, Afnan Ahmad Qureshi2, Muhammad Zaid Saeed2

  • 1Department of Internal Medicine, The Copperbelt University School of Medicine, Ndola, Zambia.

Summary

AMT-130 gene therapy offers a novel approach for Huntington's disease (HD) by reducing mutant huntingtin protein. Early clinical data suggest a potential to slow disease progression, moving beyond symptomatic treatment.

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