A Multicenter, Randomized, Double-blind, Placebo Controlled, Phase 1b/2a Study of WVE-003 Administered Intrathecally in Patients With Huntington's Disease (SELECT-HD)

  • STATUS
    Recruiting
  • days left to enroll
    84
  • participants needed
    36
  • sponsor
    Wave Life Sciences Ltd.
Updated on 20 September 2022

Summary

This is a Phase 1b/2a multicenter, randomized, double-blind, placebo-controlled study to evaluate the safety, tolerability, PK, and PD of WVE-003 in adult patients with early-manifest HD who carry the targeted single nucleotide polymorphism (SNP) - SNP3.

Details
Condition Huntington Disease
Treatment WVE-003
Clinical Study IdentifierNCT05032196
SponsorWave Life Sciences Ltd.
Last Modified on20 September 2022

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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