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Gesynta Pharma’s GS-248 Wins FDA Orphan Drug Designation

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The U.S. Food and Drug Administration (FDA) has granted orphan drug status to Gesynta Pharma’s GS-248, its oral therapy for people with systemic sclerosis (scleroderma). Orphan drug status aims to encourage therapies for rare diseases through benefits such as seven years of market exclusivity and exemption from FDA fees. “The orphan drug designation granted to our drug candidate GS-248 Click here to continue reading.

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Scleroderma Queensland is operated by Scleroderma Association of Queensland Inc., an ACNC-registered charity and Public Benevolent Institution.

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