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Therapeutic Area

Autoimmune Disorders

Therapeutic area intelligence for Autoimmune Disorders with 8 indexed intelligence signals across regulatory, clinical, competitive, and market developments.

Signals
8
Catalysts
0
Companies
2

Companies

Roche →
Sun Pharma →

Assets

ARGENX →
ENSPRYNG →
IRS2 →
LEQSELVI →
Nipocalimab →
rituximab →

Recent signals(8)

ClinicalAugust 2, 2026

Efgartigimod shows potential as maintenance therapy for iTTP in pilot study

A pilot study indicates that efgartigimod may effectively increase ADAMTS13 activity in patients with iTTP, potentially preventing relapses.

StrategyJuly 22, 2026

VIVACITY-MG3 Study Reveals High Healthcare Costs in Generalized Myasthenia Gravis Patients Treated with Nipocalimab

The VIVACITY-MG3 study highlights significant healthcare resource utilization and economic burden in adults with generalized myasthenia gravis treated with nipocalimab.

ClinicalJuly 20, 2026

Study Identifies Key Genes and Potential Therapies in Myasthenia Gravis via Lipid Metabolism Regulation

The study identified IRS2 and ALDH2 as key genes linked to lipid metabolism dysregulation in myasthenia gravis, with potential therapeutic candidates including metformin and cyclophosphamide.

ClinicalJuly 20, 2026

Study on Crisaborole Ointment and Laser Therapy for Non-Segmental Vitiligo

A study is underway to assess the efficacy of crisaborole ointment combined with 308-nm excimer laser for treating non-segmental vitiligo.

RegulatoryJuly 14, 2026

FDA Grants Priority Review for VYVGART HYTRULO Supplement by ARGENX

The FDA has granted priority review status for the supplemental application of VYVGART HYTRULO, which contains Efgartigimod Alfa and Hyaluronidase-QVFC.

RegulatoryJuly 9, 2026

FDA Accepts Supplement for LEQSELVI (Deuruxolitinib Phosphate) by Sun Pharma

The FDA has accepted a supplemental application for LEQSELVI, an investigational treatment containing Deuruxolitinib Phosphate.

RegulatoryJune 22, 2026

Nipocalimab (Imaavy) Approved for Generalised Myasthenia Gravis Treatment

Nipocalimab (Imaavy) has been authorized by the MHRA for the treatment of adults and adolescents with generalised myasthenia gravis.

RegulatoryJune 18, 2026

FDA Accepts Supplement Application for ENSPRYNG (Satralizumab)

The FDA has accepted the supplemental application for ENSPRYNG (satralizumab) submitted by Genentech.

Upcoming catalysts

No catalysts indexed for this entity yet.

Indications

Autoimmune Disorders →

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