AMRYT TO ANNOUNCE Q2 RESULTS ON AUGUST 6, 2020
DUBLIN, Ireland, and Boston MA, July 20 2020, Amryt (Nasdaq: AMYT, AIM: AMYT, Euronext Growth: AYP), a global, commercial-stage biopharmaceutical company dedicated to developing and commercializing novel therapeutics to treat patients suffering from serious and life-threatening rare diseases, today announces that the Company will issue unaudited financial results for the second quarter ended June 30, 2020 on August 6, 2020 at 1200 (BST) / 0700 (ET).
Management will host a webcast for analysts and investors on August 6 at 1330 BST / 0830 ET.
Webcast Player URL: https://edge.media-server.com/mmc/p/7ujspsgk
Telephone Dial in details:
Standard International Number |
+44 (0) 203 009 5709 |
United States |
+1 646 787 1226 |
United Kingdom (Local) |
+44 (0) 844 493 6766 |
Ireland |
+ 353 (1) 506 0626 |
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Confirmation Code |
7674874 |
A playback facility will be available from August 6, 2020 at 1830 BST – August 13, 2020 at 1830 BST. Access details as follows: Confirmation Code: 7674874 | US: + 1 917 677 7532 | UK/International:
+44 (0) 3333 00 9785 | Ireland : +353 (1) 553 8777.
Enquiries:
Amryt Pharma Plc |
+353 (1) 518 0200 |
Joe Wiley, CEO Rory Nealon, CFO/COO |
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Shore Capital |
+44 (0) 20 7408 4090 |
NOMAD and Joint Broker |
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Edward Mansfield, Daniel Bush, John More
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Stifel |
+44 (0) 20 7710 7600 |
Joint Broker |
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Jonathan Senior, Ben Maddison |
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Davy |
+353 (1) 679 6363 |
ESM Adviser and Joint Broker |
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John Frain, Daragh O’Reilly |
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Consilium Strategic Communications |
+44 (0) 20 3709 5700 |
Amber Fennell, Matthew Neal, Ashley Tapp |
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LifeSci Advisors, LLC |
+1 (212) 915 2564 |
Tim McCarthy |
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The person making this notification on behalf of Amryt is Rory Nealon, CFO/COO and Company Secretary.
About Amryt
Amryt is a biopharmaceutical company focused on developing and delivering innovative new treatments to help improve the lives of patients with rare and orphan diseases. Amryt comprises a strong and growing portfolio of commercial and development assets.
Amryt’s commercial business comprises two orphan disease products.
Juxtapid®/ Lojuxta® (lomitapide) is approved as an adjunct to a low-fat diet and other lipid-lowering medicinal products for adults with the rare cholesterol disorder, Homozygous Familial Hypercholesterolaemia ("HoFH") in the US, Canada, Columbia, Argentina and Japan (under the trade name Juxtapid®) and in the EU (under the trade name Lojuxta®). HoFH is a rare genetic disorder which impairs the body's ability to remove low density lipoprotein ("LDL") cholesterol ("bad" cholesterol) from the blood, typically leading to abnormally high blood LDL cholesterol levels in the body from before birth - often ten times more than people without HoFH - and subsequent aggressive and premature cardiovascular disease.
Myalept® / Myalepta® (metreleptin) is approved in the US (under the trade name Myalept®) as an adjunct to diet as replacement therapy to treat the complications of leptin deficiency in patients with congenital or acquired generalized lipodystrophy (GL) and in the EU (under the trade name Myalepta®) for the treatment of leptin deficiency in patients with congenital or acquired GL in adults and children two years of age and above and familial or acquired partial lipodystrophy (PL) in adults and children 12 years of age and above for whom standard treatments have failed to achieve adequate metabolic control. Metreleptin is also approved for lipodystrophy in Japan. Generalised and partial lipodystrophy are rare disorders characterised by loss or lack of adipose tissue resulting in the deficiency of the hormone leptin, produced by fat cells and are associated with severe metabolic abnormalities including severe insulin resistance, diabetes, hypertriglyceridemia and fatty liver disease.
Amryt's lead development candidate, FILSUVEZ® is a potential treatment for the cutaneous manifestations of Epidermolysis Bullosa ("EB"), a rare and distressing genetic skin disorder affecting young children and adults for which there is currently no approved treatment. FILSUVEZ® has been granted Rare Pediatric Disease Designation and has also received a Fast Track Designation from the FDA. The European and US market opportunity for EB is estimated by the Company to be in excess of $1.0 billion.
In March 2018, Amryt in-licenced a pre-clinical gene-therapy platform technology, AP103, which offers a potential treatment for patients with Recessive Dystrophic Epidermolysis Bullosa, a subset of EB, and is also potentially relevant to other genetic disorders.
For more information on Amryt, including products, please visit www.amrytpharma.com.
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