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Kamada meets end point in Phase III intravenous AAT trial

Kamada has successfully met the primary endpoint in the Phase III US clinical trials with its intravenous Alpha-1 Antitrypsin.

Alpha-1 Antitrypsin (AAT) is used to treat hereditary AAT deficiency which leads to Congenital Emphysema.

David Tsur, CEO of Kamada, said: “The company’s intravenous Alpha-1 Antitrypsin (AAT) is the only ready-to-use AAT product that does not require reconstitution before use. Concurrently, Kamada is developing the next generation AAT for various indications, to be delivered by inhalation, directly to the lungs.”