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Privosegtor Investigation in Optic Neuropathies Efficacy Evaluation Research

RecruitingPhase 3Ages 18 Years - 50 YearsAllOculis
NCT07623668 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

The goal of this clinical trial is to evaluate the safety and efficacy of privosegtor, a neuroprotective candidate, in patients diagnosed with optic neuritis (ON). Researchers will compare privosegtor and the standard of care (methylprednisolone) to a placebo and standard of care (methylprednisolone).

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📋 Eligibility rules (as published)
Key Inclusion Criteria: * Adult men and women (aged 18 to 50 years) with the first episode of ON in the study eye, associated with unilateral visual loss. * Onset of visual loss symptoms in the previous 12 days before first administration of study treatment. Key Exclusion Criteria: \- Have a history or presence of any disorder or condition that may, in the opinion of the Investigator, likely interfere with the interpretation of the study results or participant safety
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What it tests

  • Privosegtor
  • Methylprednisolone
  • Placebo
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Where

4 sites
Kahana Oculoplastic and Orbital Surgery
Livonia, United States
Medical University of South Carolina, Storm Eye Institute
Charleston, United States
UT Southwestern Medical Center (Ophthalmology CRU)
Dallas, United States
Neuro-Eye Clinical Trials
Houston, United States
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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