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Clinical Trial Summary

Paraneoplastic Neurological Syndromes are rare autoimmune complications linked to the presence of systemic cancer. Despite their autoimmune origin, they have historically shown little response to immunotherapy. The reason for this failure is probably related to too late administration of immunotherapy, at a stage where the inflammation has already disappeared and irreversible neuronal loss has occurred. The protocol focuses on patients with anti-Hu antibody sensory neuronopathy. This single arm trial consists of an early immunotherapy combining Intravenous Immunoglobulin (IVIG) for 3 months, cyclophosphamide and methylprednisolone for 6 months, at the rate of 1 cycle per month. The percentage of patients with clinical improvement will be evaluated (ONLS) at 3 months. The tolerance of the treatment will also be evaluated as well as other functional scales at 3 and 6 months.


Clinical Trial Description

n/a


Study Design


NCT number NCT06373211
Study type Interventional
Source Assistance Publique - Hôpitaux de Paris
Contact Dimitri Psimaras, MD
Phone +33 1 42 16 04 35
Email dimitri.psimaras@aphp.fr
Status Not yet recruiting
Phase Phase 2
Start date June 2024
Completion date June 2027