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RCT 2100

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Drug Profile

RCT 2100

Alternative Names: Cystic fibrosis mRNA therapeutic - ReCode Therapeutics; RCT-2100

Latest Information Update: 23 Feb 2024

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At a glance

  • Originator ReCode Therapeutics
  • Class Antifibrotics; RNA
  • Mechanism of Action Cystic fibrosis transmembrane conductance regulator expression stimulants
  • Orphan Drug Status

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

    No
  • New Molecular Entity Yes
  • Available For Licensing Yes

Highest Development Phases

  • Phase I Cystic fibrosis

Most Recent Events

  • 21 Feb 2024 ReCode announces intention to submit IND to US FDA for Cystic fibrosis for a phase I trial of RCT 2100 in the first half of 2024
  • 01 Feb 2024 Phase-I clinical trials in Cystic fibrosis (In volunteers) in New Zealand (Inhalation) (NCT06237335)
  • 01 Feb 2024 ReCode Therapeutics plans a phase I trial for Cystic Fibrosis (In volunteers) in New Zealand (PO, Inhalant) (NCT06237335)

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