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NCE-1 Intelligence & Market Opportunity

Lisraya

Brepocitinib
TYK2/JAK1 Inhibitor
NA

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
NA
Dosage Form
NA
Strength
NA
Therapeutic Category
TYK2/JAK1 Inhibitor
Usage
To treat dermatomyositis in adults
Good to know

Frequently asked questions

Why Spring Bio Solution

Intelligence you can file on

Verified regulatory data
Milestones tracked against primary FDA sources and refreshed continuously.
Analyst-built projections
Seven-year sales outlooks modeled by our pharma intelligence team.
First-to-file focus
Exclusivity windows framed around the decisions generics teams actually make.
Partnership on demand
From API sourcing to dossier support — one request starts the conversation.

Ready to act on this opportunity?

Talk to Spring Bio Solution about sourcing, licensing, and filing support for this molecule.

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