Amryt says AP101 and AP 102 clinical trials running on schedule

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Sharecast News | 04 Sep, 2017

Amryt Pharma said revenue growth exceeded management's expectations during the first half of the year amid consistent progress across the company's key commercial and development assets.

The AIM-listed company unveiled total revenues of €6.2m for the six months ended 30 June 2017, thanks mainly to an in-licensing agreement for its Lojuxta treatment.

Sales of Lojuxta, a medication for a rare, life-threatening disorder which results in unusually high levels of bad cholesterol (HoFH) ran at £5.75m, and the company's board revised upwards its estimate of the addressable market in its territories to roughly €100m.

In parallel, its lead development asset, AP 101, started its phase III clinical trials for Epidermolysis Bullosa, a rare genetic skin condition, with an interim analysis readout expected in the first half of 2018.

AP 102, a potential treatment for rate neurondocrine diseases, remained on track to commence clinical trials in humans in 2018.

Pre-clinical studies for AP 102 were expected to complete in the last quarter of 2017.

Operating losses at period-end stood at €5.79m with losses before tax reaching -€13.8m on the back of a €7.7m non-cash charge.

Cash on hand at period end stood at €10.9m with the first €10m tranche of a five-year year debt facility with the European Investment Bank having been drawn down on 3 April.

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