Geneva, March 23 -- International Clinical Trials Registry received information related to the study (NCT07453888) titled 'Efficacy and Safety of Intranasal Cenegermin in Adult Participants With Non-Arteritic Anterior Ischemic Optic Neuropathy (NAION)' on March 2.
Study Type: Interventional
Study Design:
Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Triple (Participant, Investigator, Outcomes Assessor).
Primary Sponsor: Dompe Farmaceutici S.p.A
Condition:
Non-Arteritic Anterior Ischemic Optic Neuropathy
Intervention:
Drug: Cenegermin
Recruitment Status: Not recruiting
Phase: Phase 3
Date of First Enrollment: March 2026
Target Sample Size: 272
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