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Diurnal's endocrine drug does not meet trial objective

Mon, 08th Oct 2018 09:29

(Sharecast News) - Clinical trials of Diurnal Group's Chronocort drug failed to meet the primary objective of proving superior to conventional therapy in endocrine control over a 24-hour period.Tested on 122 adults across seven countries with congenital adrenal hyperplasia who had been treated with combinations of generic steroids were randomised to either Chronocort on a twice-daily regime or continued their standard of care regimen.Chronocort achieved control on a lower overall dose of glucocorticoid with fewer patients requiring rescue therapy.A modified release formulation of Chronocort, designed to provide overnight cortisol release, eliminated the early morning peak in androgen levels seen using conventional therapy."We are surprised by these results," said Diurnal chief executive Martin Whitaker, following the previously successful Phase II clinical trial in congenital adrenal hyperplasia."However, these initial results confirm the concept of Chronocort, that early morning control of androgens can be achieved with a modified release preparation of hydrocortisone."Diurnal will now analyse the full data set from this trial, along with interim data from the ongoing Chronocort long-term dosing study, to determine next steps in the drug's development and discuss these with the regulatory authorities."We remain confident that Chronocort will be a valuable treatment option for CAH patients," Whitaker said.Diurnal, in which IP Group is a major shareholder, recently bagan a Phase III study in congenital adrenal hyperplasia in the USA, focussed particularly on morning control of androgens.
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Diurnal agrees special protocol with FDA for Chronocort study

(Sharecast News) - Specialty pharmaceutical company Diurnal announced on Monday that the US Food and Drug Administration (FDA) has agreed a special protocol assessment (SPA) for 'Chronocort', or modified-release hydrocortisone, for the design, endpoints and statistical analysis approach of a pivotal study of the product, for the treatment for congenital adrenal hyperplasia (CAH).

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Diurnal gets UK approval for 'Efmody' treatment

(Sharecast News) - Speciality pharmaceutical company Diurnal Group announced on Friday that the UK Medicines and Healthcare products Regulatory Agency (MHRA) has granted a marketing authorisation for 'Efmody', or hydrocortisone modified-release hard capsules, as treatment for adult and adolescent patients with the rare congenital adrenal hyperplasia (CAH) condition.

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Diurnal granted European patent for Alkindi

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