
Addressing the True Burden of CIDP in Clinical Practice: Karen Lynch, MD, MRCPI
The senior global medical director at Sanofi discussed the ongoing burden of CIDP, highlighting diagnostic challenges, treatment gaps, and the need for improved biomarkers and emerging therapies. [WATCH TIME: 3 minutes]
WATCH TIME: 3 minutes
“CIDP is still fundamentally a clinical diagnosis, and that creates real challenges. Without a clear biomarker, even experienced neurologists can struggle, and delays in diagnosis ultimately impact long-term patient outcomes.”
Chronic inflammatory demyelinating polyneuropathy (CIDP) is a rare, immune-mediated neuropathy characterized by progressive weakness, sensory dysfunction, and impaired mobility due to demyelination of peripheral nerves. Although considered a treatable condition, CIDP remains associated with substantial long-term disability, particularly when diagnosis and treatment are delayed.¹ Early recognition is critical, as timely intervention can help prevent irreversible nerve damage and improve functional outcomes.
Despite the availability of established therapies, including intravenous immunoglobulin (IVIg), corticosteroids, and plasma exchange, treatment response in CIDP is often variable. A meaningful proportion of patients either fail to respond to first-line therapy or experience only partial improvement, underscoring the need for more effective and durable treatment strategies.² In parallel, emerging therapeutic approaches, including targeted immunomodulatory agents such as complement inhibitors, are being investigated to address persistent disease activity and unmet clinical needs.
At the














