UK TRADING UPDATE SUMMARY: Integumen Kicks Off Covid-19 Skin Trials
UK TRADING UPDATE SUMMARY: Integumen Kicks Off Covid-19 Skin Trials
Read moreUK TRADING UPDATE SUMMARY: Integumen Kicks Off Covid-19 Skin Trials
Read moreAmryt Pharma Cheers Strong 2019 And Beats Expectations So Far In 2020
Read moreUK TRADING UPDATE SUMMARY: Braemar Says Oil Tankers Wanted For Storage
Read moreAmryt Pharma Financially Strong, Revenue Rises More Double Digits
Read moreAmryt Pharma Shares Rise As It Cheers Aegerion Acquisition Synergies
Read more(Sharecast News) - Amryt Pharma updated the market on its trading update for the nine months ended 30 September on Tuesday, noting that it had completed the transaction to acquire Aegerion Pharmaceuticals on 24 September.
Read moreAmryt Pharma Revenue Rises On Performance From Two New Assets
Read moreAmryt Pharma Skin Condition Drug Gets US FDA Fast Track Designation
Read more(Sharecast News) - Biopharmaceutical company Amryt Pharma announced on Tuesday that the US Food and Drug Administration (FDA) has designated the investigation of 'AP101' - Oleogel-S10 - for the treatment of epidermolysis bullosa (EB) as a 'Fast Track' development programme.
Read moreAmryt Pharma Loss Widens On Aegerion Deal Costs; Lojuxta Revenue Rises
Read moreAmryt Pharma Completes Combination With Aegerion Pharmaceuticals
Read moreAmryt Pharma Shares Temporarily Suspended On Aegerion Buy
Read moreLONDON (Alliance News) - Amryt Pharma PLC on Tuesday said it has agreed the all-paper acquisition of Aegerion Pharmaceuticals, a subsidiary of Novelion Therapeutics Inc, and intends to raise USD60
Read moreLONDON (Alliance News) - Amryt Pharma PLC on Wednesday said its annual loss narrowed as a result of increased revenue from its drug Lojuxta.The company's pretax loss shrank to EUR25.7
Read more(Sharecast News) - Orphan drug company Amryt Pharma updated the market on its phase 3 'EASE' trial for AP101 as a potential treatment for epidermolysis bullosa (EB) on Thursday, reporting that following an assessment by the trial's independent data monitoring committee, it could now enrol infants and children with EB between the ages of 21 days to four years in the trial.
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