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aBLA Filing Intelligence & Biosimilar Opportunity

Adbry

Tralokinumab-Ldrm
Dermatologic
Injection Injectable

Atopic dermatitis biology implicates both IL-4 and IL-13, and whether blocking IL-13 alone would suffice was an open question. Adbry (tralokinumab) tested it commercially.

Tralokinumab specifically targets and neutralizes IL-13, preventing it from binding its receptors, in contrast to dupilumab’s blockade of the shared IL-4 receptor alpha subunit. The subcutaneous injection treats moderate-to-severe atopic dermatitis not adequately controlled with topical therapies.

Adbry has since expanded into adolescents and faces no biosimilar competition, but it competes against an entrenched market leader and newer oral JAK inhibitors. Its selectivity argument and conjunctivitis rate relative to dupilumab are the differentiators worth tracking.

Approval Date
27-Dec-21
Data Exclusivity Expiry
27-Dec-25
Market Exclusivity Expiry
27-Dec-33
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
Tralokinumab-Ldrm
Innovator
LEO PHARMA INC.
Dosage Form
Injection Injectable
Strength
150 mg/mL
Therapeutic Category
Dermatologic
Usage
To treat moderate-to-severe atopic dermatitis
Good to know

Frequently asked questions

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