Feasibility Study - SINAPPS-1
Feasibility and acceptability of immunotherapy in antibody positive FEP
We are developing a completely new approach to the investigation and treatment of people with the major neuropsychiatric disorder, schizophrenia. SINAPPS group aims to treat people who test positive for NMDAR (and other similar) antibodies in a similar way to people diagnosed with autoimmune encephalitis, using immunological methods.
The SINAPPS-1 study aims at determining which treatment is considered by participants as the most acceptable and least invasive, while still being effective in removing pathogenic antibodies.
These findings will then be applied in the SINAPPS 2 study.
SINAPPS 1 completed recruitment on July 2017.
This study was funded by the Stanley Medical Research Institute.
Clinical Trial - SINAPPS-2
A randomised phase II double-blinded placebo-controlled trial of intravenous immunoglobulins and rituximab in patients with antibody-associated psychosis
The SINAPP2 randomized clinical trial will investigate the use of Intravenous Immunoglobulin (IVIG) and Rituximab as a treatment for symptoms of psychosis in antibody positive patients. The study will take place in 8 different sites across England to make it accessible to as many participants as possible.
Recruitment began in July 2017 and the study will run until 2021.
Click here for more information.
This trial is funded by the Medical Research Council.
SINAPPS-1 was a feasibility study, involving a very small number of patients. In this study we aimed to identify the most acceptable treatment to eliminate pathogenic antibodies.
SINAPPS-2 is a larger study involving participants from all across England, testing the efficacy and safety of immunotherapy in persons suffering from antibody-induced symptoms of psychosis.
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