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A Double-blind, Randomized, Placebo Controlled, Trial to Assess Safety and Efficacy of SLS-005 (Trehalose Injection, 90.5 mg/mL for Intravenous Infusion) for the Treatment of Adults With Spinocerebellar Ataxia

Trial Profile

A Double-blind, Randomized, Placebo Controlled, Trial to Assess Safety and Efficacy of SLS-005 (Trehalose Injection, 90.5 mg/mL for Intravenous Infusion) for the Treatment of Adults With Spinocerebellar Ataxia

Status: Discontinued
Phase of Trial: Phase II/III

Latest Information Update: 29 Apr 2024

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At a glance

  • Drugs Trehalose (Primary)
  • Indications Spinocerebellar ataxias
  • Focus Registrational; Therapeutic Use
  • Acronyms STRIDES
  • Sponsors Seelos Therapeutics

Most Recent Events

  • 22 Apr 2024 Status changed from suspended to discontinued.
  • 22 Dec 2023 Results (n=22) were presented in a Seelos Therapeutics Media Release.
  • 29 Mar 2023 According to a Seelos Therapeutics media release, Seelos is temporarily pausing additional enrollment of patients in the SLS-005-302 study in spinocerebellar ataxia type 3 (SCA3). Patients already enrolled will continue in the study and data will continue to be collected in order to make decisions for resuming enrollment in the future

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