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NCE-1 Intelligence & Market Opportunity

Lisraya

Brepocitinib
TYK2/JAK1 Inhibitor
Oral Tablet

Dermatomyositis can affect both physical strength and quality of life, yet treatment options specifically developed for the condition have remained limited. Lisraya (brepocitinib) introduces a new oral treatment option for adults living with this rare autoimmune disease.

Its approval represents an important step in the development of targeted therapies for dermatomyositis and adds a new option to the treatment landscape.

For clinical trial and first-to-file teams working in autoimmune and rare disease research, monitoring Lisraya’s adoption, exclusivity, and availability could become increasingly relevant.

Approval Date
27-Aug-26
NCE-1 Date
27-Aug-30
NCE Date
27-Aug-31
Commercial snapshot

Market performance & projections

Revenue ($M)
NA
CAGR (%)
NA
Projected sales, 2026–2032 ($M)
Analyst projection, $M per year
2026
NA
2027
NA
2028
NA
2029
NA
2030
NA
2031
NA
2032
NA
Molecule profile

Details & specifications

Molecule
Brepocitinib
Innovator
PRIOVANT THERAPEUTICS INC
Dosage Form
Oral Tablet
Strength
EQ 30mg base
Therapeutic Category
TYK2/JAK1 Inhibitor
Usage
To treat dermatomyositis in adults
Good to know

Frequently asked questions

Ready to act on this opportunity?

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