RecruitingPhase 2NCT06510283

Efficacy and Safety of Taitacept in Treatment of Refractory or Recurrent Anti-NMDAR/anti-LGI1 Encephalitis


Sponsor

Beijing Tongren Hospital

Enrollment

10 participants

Start Date

Dec 1, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The main objective is to explore the efficacy and safety of Telitacicept in the treatment of refractory/recurrent anti-NMDAR and anti-LGI1 encephalitis. Through this prospective, single-center, open-label clinical trial, we aim to investigate the effectiveness and safety of Telitacicept in refractory/recurrent anti-NMDAR and anti-LGI1 encephalitis by add-on therapy of Telitacicept combined with traditional treatment.


Eligibility

Min Age: 14 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a drug called Taitacept (telitacicept) for patients with autoimmune encephalitis — a serious brain condition where the immune system mistakenly attacks the brain — specifically the anti-NMDAR or anti-LGI1 subtypes that have not responded well to standard treatments. **You may be eligible if...** - You are 14 years or older - You have been diagnosed with autoimmune encephalitis (anti-NMDAR or anti-LGI1 type) within the past 9 months - Your symptoms include at least four of the following: behavioral or cognitive changes, speech problems, seizures, abnormal movements, reduced consciousness, or autonomic problems - Your disease has not adequately responded to first-line immunotherapy treatments **You may NOT be eligible if...** - You have a different type of autoimmune encephalitis not included in this study - You have active severe infections or other serious illnesses - You have received certain medications that would interfere with the study drug - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGTaitacept

Telitacicept will be subcutaneously injected at a dose of 240mg per week, lasting for at least 24 weeks.


Locations(1)

Beijing Tongren Hospital,Capital Medical University

Beijing, Beijing Municipality, China

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NCT06510283


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