Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**MOG-modified autologous CD4+ T cells** are a form of cell therapy in which a patient's own CD4+ T cells are genetically modified to recognize the myelin oligodendrocyte glycoprotein (MOG) antigen. MOG is associated with autoimmune demyelinating diseases such as MOG antibody-associated disease (MOGAD). These cell therapies are designed to alter the immune response by specifically targeting MOG, aiming to either modulate or suppress autoreactive T cell responses implicated in disease pathology. Although multiple types of MOG-specific T cell therapies have been described in experimental and early clinical contexts, current clinical evidence for MOG-target-modified T cell therapies is extremely limited. No fully characterized, named, or commercialized product with this exact specification appears to be in late-stage clinical use or approved as of September 2025.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on MOG-modified autologous CD4+ T cells.