Diurnal Looking To Secure US Partner Soon For Alkindi

Hypogonadism Capsule Also Promising

With its adrenal insufficiency therapy Alkindi getting established in Europe, the UK biotech is in partnering discussions in the US where approval is expected before the end of the year.

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US could be land of opportunity for Diurnal • Source: Shutterstock

Following the successful launch of Alkindi in a number of European countries, the UK's Diurnal Group PLCis laying the groundwork for a US launch for the replacement therapy for adrenal insufficiency in infants.

The biotech, one of the very few in the UK to have taken a product from concept to commercialization on its own, has unveiled its plans for Alkindi (immediate-release hydrocortisone) across the Atlantic and reflected on its progress closer to home. Approved two years ago through the European Medicines Agency's pediatric-use marketing authorization (PUMA) pathway, Alkindi was initially launched in Germany, the UK and Austria and is now also available in Sweden, Denmark, Norway, Iceland and since last week Italy

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