Privosegtor Investigation in Optic Neuropathies Efficacy Evaluation Research
Purpose
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).
Condition
- Optic Neuritis
Eligibility
- Eligible Ages
- Between 18 Years and 50 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
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.
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
Study Design
- Phase
- Phase 3
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel Assignment
- Primary Purpose
- Treatment
- Masking
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental Privosegtor |
|
|
|
Placebo Comparator Placebo |
|
Recruiting Locations
Kahana Oculoplastic and Orbital Surgery
Livonia, Michigan 48152
Livonia, Michigan 48152
Neuro-Eye Clinical Trials
Houston, Texas 77074
Houston, Texas 77074
More Details
- Status
- Recruiting
- Sponsor
- Oculis