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Amryt Pharma given go-ahead to continue Phase III EASE trial

Fri, 04th Jan 2019 14:41

(Sharecast News) - Revenue-generating orphan drug company Amryt Pharma announced the results of an unblinded interim efficacy analysis on its pivotal Phase III EASE trial for AP101 as a potential treatment for Epidermolysis Bullosa (EB) on Friday.The London-listed firm said the analysis was conducted by an independent data monitoring committee, which recommended that the trial should continue with an increase of 48 patients in the study to a total of 230 evaluable patients, in order to achieve 80% statistical power.It said the analysis was conducted using unblinded efficacy data received by the IDMC for the primary endpoint from the first half of the study.Amryt said it would begin the recruitment process for the additional patients required, and now expected a readout of the top line data from the EASE study in the second half of 2019.Following the announcement, Amryt said it was now in a position to draw down the remaining €5m of its European Investment Bank facility."The IDMC's recommendation is good news for Amryt as it allows us to continue the trial with only a modest increase in the size of the study," said chief executive officer Joe Wiley."This brings us closer to potentially delivering a treatment for patients with EB."Wiley thanked the patients, families and clinical investigators involved in the EASE trial to date."Today's news is a significant milestone for Amryt and our shareholders in building towards our vision of becoming a global leader in rare and orphan diseases."
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19 Dec 2019 14:13

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5 Nov 2019 11:09

Amryt Pharma upbeat on progress in first nine months of year

(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.

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5 Nov 2019 10:23

Amryt Pharma Revenue Rises On Performance From Two New Assets

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1 Oct 2019 18:49

Amryt Pharma Skin Condition Drug Gets US FDA Fast Track Designation

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1 Oct 2019 15:08

Amryt gets FDA fast track for Oleogel-S10

(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.

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30 Sep 2019 18:49

Amryt Pharma Loss Widens On Aegerion Deal Costs; Lojuxta Revenue Rises

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25 Sep 2019 12:24

Amryt Pharma Completes Combination With Aegerion Pharmaceuticals

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24 Sep 2019 15:00

Amryt Pharma Shares Temporarily Suspended On Aegerion Buy

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21 May 2019 12:35

Amryt Pharma Agrees To All-Paper Acquisition Of Aegerion (ALLISS)

LONDON (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

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17 Apr 2019 11:17

Amryt Pharma Loss Narrows On Revenue From Cholesterol Drug Lojuxta

LONDON (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

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28 Feb 2019 14:39

Amryt gets approval to extend EASE trial to infants and children

(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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