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An autoimmune acute encephalitis caused by antibodies against the glutamate NMDA receptor. It usually affects females and in the majority of cases it is associated with the presence of a tumor, most commonly an ovarian teratoma. The presence of a tumor in patients with this form of encephalitis implies that the latter is a paraneoplastic syndrome. It is manifested with psychiatric symptoms and epileptic seizures. It is a potentially lethal disorder; however, it is usually reversible with the prompt removal of the tumor.
Biomarker and diagnostic research for anti-NMDA receptor encephalitis has been reported in the published literature.
No approved treatments are currently available for anti-NMDA receptor encephalitis. An additional 1 compound holds orphan drug designation.
While no drugs are FDA-approved specifically for anti-NMDA receptor encephalitis, some of the following designated compounds may be used off-label in clinical practice. Treatment decisions should be made in consultation with a specialist familiar with this condition.
The following drugs have received orphan drug designation from the FDA for anti-NMDA receptor encephalitis. Orphan designation reflects regulatory interest and does not indicate approval for treatment.
Brand Name | Generic Name | Sponsor |
|---|
Estimated prevalence: Unknown (Unknown prevalence).
2 clinical trials registered, 1 recruiting. Interventions under study include drug therapy. Pipeline includes 1 PHASE2, 1 NA. Research is primarily sponsored by academic and government institutions.
141 publications have been identified in PubMed for anti-NMDA receptor encephalitis. Research spans Case Report / Case Series (43%), Review / Meta-Analysis (16%), and Epidemiology / Natural History (11%).
Research Type | Count | % of Total |
|---|---|---|
Patient case studies | 61 |
Data assembled from 5 of 12 sources · Last updated Sep 20, 2026, 1:00 AM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Designated
Exclusivity End |
|---|
Designation Status |
|---|
Humanized one-armed monoclonal antibody | Humanized one-armed monoclonal antibody | Arialys Therapeutics, Inc. | 2022 | — | Designated |
Gene therapy approaches for anti-NMDA receptor encephalitis have been reported in the published literature.
2 trials found
Research summaries | 23 | 16% |
Disease patterns and progression | 15 | 11% |
Testing and diagnosis research | 14 | 10% |
Other research | 11 | 8% |
Laboratory research | 9 | 6% |
Clinical study results | 7 | 5% |
New treatment approaches | 1 | 1% |
Mengistu T (2026). [PMID: 41641166](https://pubmed.ncbi.nlm.nih.gov/41641166/). *Clin Case Rep*. [Basic Science / Preclinical]
Amemiya T (2026). [PMID: 41729962](https://pubmed.ncbi.nlm.nih.gov/41729962/). *QJM*. [Diagnostic / Biomarker]
Khamis MM (2026). [PMID: 41991229](https://pubmed.ncbi.nlm.nih.gov/41991229/). *BMJ Case Rep*. [Case Report / Case Series]
Samanta D (2026). [PMID: 31869136](https://pubmed.ncbi.nlm.nih.gov/31869136/). *Unknown Journal*. [Review / Meta-Analysis]
Jin M (2026). [PMID: 42214057](https://pubmed.ncbi.nlm.nih.gov/42214057/). *Neurol Neuroimmunol Neuroinflamm*. [Epidemiology / Natural History]
Choi HB (2026). [PMID: 41953803](https://pubmed.ncbi.nlm.nih.gov/41953803/). *Brain Neurorehabil*. [Case Report / Case Series]
Siladji D (2026). [PMID: 42200857](https://pubmed.ncbi.nlm.nih.gov/42200857/). *Reports (MDPI)*. [Case Report / Case Series]
Yoong W (2026). [PMID: 41633558](https://pubmed.ncbi.nlm.nih.gov/41633558/). *Asian J Endosc Surg*. [Case Report / Case Series]
Lee ST (2026). [PMID: 41864220](https://pubmed.ncbi.nlm.nih.gov/41864220/). *Lancet Neurol*. [Review / Meta-Analysis]
Moin-Ud-Din-Arshad M (2026). [PMID: 42078602](https://pubmed.ncbi.nlm.nih.gov/42078602/). *Ann Med Surg (Lond)*. [Case Report / Case Series]
AI-curated news mentioning anti-NMDA receptor encephalitis
Updated May 1, 2026
A recent study highlights the diagnostic and therapeutic challenges in managing anti-NMDA receptor encephalitis linked to ovarian immature teratoma. This research underscores the complexities faced by clinicians in treating this rare neurological condition.