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Eton Pharmaceuticals acquires U.S. rights to ASN-001 for infantile hemangioma, aiming FDA approval by 2028

Company Fundamentals
05 Aug 2026
GlobeNewsWire
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Bullish
Eton Pharmaceuticals acquires U.S. rights to ASN-001 for infantile hemangioma, aiming FDA approval by 2028

Eton Pharmaceuticals has licensed U.S. rights to ASN-001, a late-stage topical gel targeting moderate infantile hemangiomas, a condition currently treated off-label with ophthalmic timolol. ASN-001 complements Eton's existing oral solution HEMANGEOL, potentially covering the full spectrum of infantile hemangioma patients. Phase II/III trials showed significant efficacy, with up to 56% elimination or near-elimination at 24 weeks. Eton plans to submit a New Drug Application in the second half of 2027, aiming for FDA approval and launch in 2028, targeting an estimated 20,000 to 30,000 patients annually and expanding its pediatric dermatology portfolio.

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