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Farabursen - Regulus Therapeutics

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Drug Profile

Farabursen - Regulus Therapeutics

Alternative Names: RGLS-8429

Latest Information Update: 09 Apr 2025

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At a glance

  • Originator Regulus Therapeutics
  • Class Antisense oligonucleotides; MicroRNAs
  • Mechanism of Action Gene silencing; MIRN17 microRNA expression inhibitors
  • Orphan Drug Status

    Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

    Yes - Autosomal dominant polycystic kidney disease
  • New Molecular Entity No

Highest Development Phases

  • Phase I Autosomal dominant polycystic kidney disease

Most Recent Events

  • 27 Mar 2025 Regulus Therapeutics plans a pivotal phase III trial in Autosomal dominant polycystic kidney disease in the third quarter of 2025
  • 26 Mar 2025 Updated pharmacodynamics data from a phase I trial in Autosomal dominant polycystic kidney disease released by Regulus Therapeutics
  • 08 Oct 2024 Regulus Therapeutics plans a pivotal phase III trial in Autosomal dominant polycystic kidney disease

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