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Skytrofa

Lonapegsomatropin-Tcgd
Hormonal therapy
Injection Injectable

Growth hormone deficiency has meant daily injections for children, a burden that erodes adherence over years of treatment. Skytrofa (lonapegsomatropin) was among the first long-acting alternatives approved in the U.S.

It is a prodrug in which somatropin is bound to a carrier and released gradually through a cleavable linker, producing sustained exposure from a single weekly dose. The injection is approved for children 1 year and older with growth hormone deficiency who weigh at least 11.5 kg.

Skytrofa faces no biosimilar competition but competes directly with other weekly growth hormones approved around the same period. Conversion from daily somatropin and long-term growth outcome data are the decisive factors for uptake in a market with entrenched incumbents.

Approval Date
25-Aug-21
Data Exclusivity Expiry
25-Aug-25
Market Exclusivity Expiry
25-Aug-33
Commercial snapshot

Market performance & projections

Revenue ($M)
232
CAGR (%)
21.53%
Projected sales, 2026–2032 ($M)
Analyst projection, $M per year
2026
275
2027
343
2028
409
2029
506
2030
587
2031
674
2032
742
Molecule profile

Details & specifications

Molecule
Lonapegsomatropin-Tcgd
Innovator
ASCENDIS PHARMA ENDOCRINOLOGY, INC.
Dosage Form
Injection Injectable
Strength
3 mg, 11 mg, 7.6 mg, 5.2 mg, 3.6 mg, 13.3 mg, 9.1 mg, 6.3 mg, 4.3 mg
Therapeutic Category
Hormonal therapy
Usage
To treat short stature due to inadequate secretion of endogenous growth hormone Drug Trial Snapshot
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Frequently asked questions

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