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Evaluation of the Safety and Efficacy of Secukinumab in the Treatment of Recurrent Myelin Oligodendrocyte Glycoprotein Antibody-Positive Optic Neuritis

Evaluation of the Safety and Efficacy of Secukinumab in the Treatment of Recurrent Myelin Oligodendrocyte Glycoprotein Antibody-Positive Optic Neuritis

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500100442
Enrollment
Unknown
Registered
2025-04-09
Start date
2023-02-16
Completion date
Unknown
Last updated
2025-04-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Optic Neuritis

Interventions

Treatment group:Scheduled injection of Secukinumab

Sponsors

Chinese People's Liberation Army General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1, Age >=8 years old, and <=65 years old; 2. The clinical diagnosis was recurrent MOG-Ab positive ON; 3. Positive for MOG-Ab in Serum detected by CBA method (titer over 1:10 considered positive); 4. Patients can sign informed consent by themselves

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women; 2. Patients who have used other biologics (including Rituximab) within 3 months prior to the current onset of illness; 3. Patients with a recent plan for vaccination; 4. Heart disease; 5. Infectious diseases; 6. White blood cell count 14000 × 10^9/L before corticosteroid therapy during the acute phase; 7. Participants considered unsuitable for this clinical trial for other reason

Design outcomes

Primary

MeasureTime frame
The interval between disease relapses;

Secondary

MeasureTime frame
vision;Optical Coherence Tomography;Peripheral Blood T-cell Detection;

Countries

China

Contacts

Public ContactShihui Wei

Chinese People's Liberation Army General Hospital

weishihui706@hotmail.com+86 188 0147 8734

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026