What Can You Expect at the Premier Autoimmune Neuromuscular & Nerve Disorders Forum in 2026?
The Autoimmune Neuromuscular & Nerve Disorders Drug Development Summit is your opportunity to step inside one of the fastest-evolving areas in biopharma and engage directly with the leaders shaping its future. Over three days, you’ll gain a deep, mechanism-driven understanding of diseases like Myasthenia Gravis, CIDP, GBS and MMN, going beyond surface-level updates to explore the biology, biomarkers and translational challenges defining success.
Expect cutting-edge insights on emerging therapeutic approaches, honest discussions around what’s not working, and practical strategies to differentiate in an increasingly competitive landscape. Through a mix of data-led presentations, interactive roundtables and high-value networking, you’ll leave with the clarity, connections and confidence needed to advance your pipeline and capitalise on this transformative moment in autoimmune neuromuscular drug development.
Unmissable Event Highlights
Rethinking Preclinical Models to Improve Clinical Success
Challenge the limitations of current in vitro and in vivo models across MG, CIDP, GBS and MMN, and uncover how poor disease representation is driving translational failure. Gain practical frameworks to redefine what “good” preclinical evidence looks like and ensure early signals truly predict clinical efficacy.
With Expert Insights from:
Cracking MG Subtypes to Enable Precision Therapies
Dive into the distinct biology of AChR-positive versus MuSK-positive MG to understand how mechanistic differences should shape therapeutic strategy. Learn how aligning drug modality to subtype can improve responder rates and optimise clinical trial design.
With Expert Insights From:
Winning in a Crowded MG Market Through Smarter Positioning
Explore how emerging mechanisms, from FcRn to CAR-, can be strategically positioned in an increasingly saturated landscape. Identify how to differentiate your asset, sequence therapies effectively, and target patients who fail existing treatments.
With Expert Insights From:
Reframing Autoantibodies to Unlock Better Diagnostics & Treatments
Move beyond simply reducing antibody levels to understand their true role in disease. Examine the limitations of “seronegativity,” uncover new autoantibody targets, and refine patient stratification to enable more precise, biology-driven development.
With Expert Insights From:
Redefining CIDP: From Clinical Label to Biological Disease
Interrogate CIDP as a poorly defined syndrome and uncover why heterogeneity is undermining trial success. Discover how biomarker-driven stratification and immunophenotyping can transform trial design and unlock meaningful clinical outcomes.
With Expert Insights From:
Transforming Target Discovery with Better Data & Models
Learn how to overcome flawed discovery systems by integrating multi-omics, AI-driven insights and clinically relevant biomarkers. Improve early target validation and prioritisation to reduce late-stage failure in neuromuscular drug development.
With Expert Insights From:
Attending Companies Include