In a statement, Joe Wiley, Amryt Pharma’s chief executive, said: “We are very excited to report NICE’s approval which will now give all England and Wales based patients suffering from … Mr. Stafford has worked in the pharmaceutical industry for thirty years. You may opt out if you wish. You can also contact MarketWatch Customer Service via our Customer Center. Dr.Vink has significant experience as a senior executive having worked in the pharmaceutical industry for more than 30 years. Kieran Rooney VP, Strategic Alliances and Licensing. Dr Joe Wiley, CEO of Amryt Pharma, commented today: “We are very excited to report NICE’s approval of Myalepta® which will now give all England and Wales based patients suffering from … Dr. Wiley opened and led the European office of Sofinnova Ventures Inc. Dr Joe Wiley, CEO of Amryt Pharma, commented today: " We are pleased that ANVISA has recognised the significant unmet medical need of patients in Brazil suffering from HoFH and have … Dec 23, 2020 (GLOBE NEWSWIRE via COMTEX) -- Amryt Receives Reimbursement Approval from NICE for Myalepta® (metreleptin) in England and Wales DUBLIN, Ireland, and Boston MA, January 20, 2021, Amryt (Nasdaq: AMYT, AIM: AMYT), a global, … Forward-looking statements involve inherent known and unknown risks, uncertainties and contingencies because they relate to events and depend on circumstances that may or may not occur in the future and may cause the actual results, performance or achievements to be materially different from those expressed or implied by such forward-looking statements. He has led organisations through significant operational transformation and been involved in acquisitions of companies and product portfolios. Joe Wiley, CEO of Amryt Pharma, commented:"Receiving an orphan drug designation from the FDA for our gene-therapy candidate, AP103, is a significant development for patients suffering from EB and provides additional momentum to our development pipeline. Prior to joining, she was Medical Director EMEA at Aegerion Pharmaceuticals, where she was responsible for the medical activities supporting Lojuxta (lomitapide), a treatment for Homozygous Familial Hypercholesterolaemia (HoFH). He has been a member of the Scientific Committee of the French drug agency. He has almost 20 years’ experience across the pharmaceutical, medical devices and biotech industries, both in the US and UK. Dr Joe Wiley, CEO of Amryt Pharma, commented today: “We are very pleased that the Ministry of Health in the Kingdom of Saudi Arabia has approved the reimbursement of Lojuxta® which … In September and October 2020, Amryt reported positive results from its pivotal global Phase 3 trial in EB. He has had a diverse and distinguished legal career, evenly split between private practice and public service. She joined Amryt in June 2019. By continuing to surf this website you explicitly agree to the use of cookies on this website. He was previously a medical director at Astellas Pharma Limited where he liaised with the marketing team and was involved in the launch of a number of specialty pharmaceutical products. Is there a problem with this press release? Mr. Wills also served as the lead director of Derma Sciences, Inc. until December 2015 and as Chief Financial Officer from 1997 to 2000. In March 2018, Amryt in-licensed a pre-clinical gene-therapy platform technology, AP103, which offers a potential treatment for patients with Dystrophic Epidermolysis Bullosa, a subset of EB, and is also potentially relevant to other genetic disorders. Rory Nealon Chief Financial Officer and Chief Operating Officer (CFO & COO), Chief Financial Officer and Chief Operating Officer (CFO & COO). Dr Joe Wiley, CEO of Amryt Pharma, commented today: “We are very excited to report NICE’s approval of … Amryt's lead development candidate, FILSUVEZ(R) (Oleogel-S10) 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. Earlier in his career he held several leadership positions across the industry, including Head of Global Biopharmaceuticals for the Sandoz division of the Novartis Group, Vice President International Business for Biogen Inc., and Head of Worldwide Marketing, Cardiovascular and Thrombosis at Sanofi-Synthelabo Ltd. Dr.Vink also served as a member of the Executive Committee of the European Federation of Pharmaceutical Industries and Associations between 2013 and 2015. Dr Joe Wiley, CEO of Amryt Pharma, commented today: “We are very excited to report NICE’s approval of Myalepta® which will now give all England and Wales based patients suffering from … Dr. Vink also serves as Chairman of venture capital backed NMD Pharma ApS, a neurology biopharma company in Denmark and F2G Ltd, a rare fungal disease UK- and Austria-based company. Juxtapid(R)/ Lojuxta(R) (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(R)) and in the EU and Brazil (under the trade name Lojuxta(R)). These statements are not guarantees of future performance or the ability to identify and consummate investments. Gerry has over 25 years’ experience in the pharmaceutical sector. The MarketWatch News Department was not involved in the creation of this content. Dr Joe Wiley, CEO of Amryt, commented: “2019 was a truly transformational year for Amryt. Listed on London’s Alternative Investment Market and the Nasdaq, Amryt is headed by chief executive and founder Joe Wiley. Dr Joe Wiley, CEO of Amryt Pharma, commented today: “We are very pleased that the Ministry of Health in the Kingdom of Saudi Arabia has approved the reimbursement of Lojuxta® which … Amryt’s Myalepta scores NICE backing for rare lipid disorder. Dr. Munoz worked with the Fournier Group, as Research and Development director and then Senior Vice President of the Pharmaceutical Division. She has a degree in Medicine from Bristol University Medical School and spent six years in the NHS in General Practice. Dr. Joe Wiley Chief Executive Officer (CEO). Gerry Gilligan Head of Manufacturing Supply Chain. Mr. Stafford retired in 2014 following the sale of Forest Laboratories, Inc. to Actavis Plc (now Allergan Plc) in a US $28 billion transaction where Mr. Stafford was Executive Vice President of Global Marketing. He was also responsible for EMEA marketing and market access. Separately, Mr. Stafford was founder of what is today one of Ireland’s leading multi-channel sales, marketing and distribution service providers approved by the Irish Medicines Board (now The Health Products Regulatory Authority) to service the wholesale and retail trade. He was Chairman, Chief Executive Officer and majority shareholder of the Tosara Group who owned, manufactured and marketed the successful international brand Sudocrem. Her former experience has included working as HR Director in Total mobile, TV3 and Oxigen. Myalept(R) / Myalepta(R) (metreleptin) is approved in the US (under the trade name Myalept(R)) 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(R)) 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. He holds a BSc. The product has been granted Rare Pediatric Disease Designation and has also received a Fast Track Designation from the U.S. Food and Drug Administration. Between 2007 and 2017, he worked with over 30 pharmaceutical, biotechnology and professional service companies, including, most recently, Amakem Therapeutics and PwC. This site uses cookies as described in our privacy statement to improve your experience. AP103 is based on a new gene therapy delivery platform, in-licensed by Amryt in March 2018, that utilises a non-viral delivery vector, HPAE (Highly Branched Poly B-Amino Ester), designed to deliver the correct collagen VII gene into skin cells. Myalepta® received marketing authorisation from the European Medicines Agency (“EMA”) in 2018. Now my brother wants half, COVID-19 may accelerate these 3 trends in real estate, Nasdaq touches record high but Dow lags in Monday morning trade as investors brace for busiest week of earnings. Rory Nealon co-founded Amryt Pharma in August 2015. Dr. Wiley opened and led the European office of Sofinnova Ventures Inc. Julie has over 25 years’ experience in HR. David Allmond Chief Commercial Officer (CCO). He has a PhD in Neuropharmacology from the University of Wales, Cardiff. No person is under any obligation to update or keep current the information contained in this announcement or to provide the recipient of it with access to any additional relevant information that may arise in connection with it. He spent nine years in clinical practice in the NHS, specialising in cardiovascular surgery and physiology, having qualified as a medical doctor at the University of London. Mr. Stafford held numerous senior positions within that corporation including Chief Executive Officer of Forest UK and Ireland as well as Chief Executive Officer of Forest Laboratories Europe since 1999. Dr.Wiley will continue as Chief Executive Officer of the Enlarged Group for no less than two years after Closing, unless he resigns or is removed from the position by a vote of a majority of the Board. 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. In addition, Dr. Vink is a board member at Santhera AG and Spero Therapeutics Inc and since 2019 began working with Athyrium as a Senior Advisor. Stephen joined Amryt Pharma as VP, Global Marketing in December 2018 with over 15 years’ experience in the pharmaceutical industry across multiple therapy areas. Mr.Wills serves as the Chief Financial Officer, since 1997, and Chief Operating Officer, since 2011, of Palatin Technologies, Inc., a biopharmaceutical company developing targeted, receptor-specific peptide therapeutics for the treatment of diseases with significant unmet medical need and commercial potential. The FDA's Office of Orphan Products Development ("OOPD") grants orphan drug designation to support the development of medicines for rare diseases, that affect fewer than 200,000 people in the United States. Prior to that, he was the Chief Financial Officer (from 2003), Chief Operating Officer (from November 2007) and Board Member of Trinity Biotech plc, a diagnostic company listed on Nasdaq. Mr. Stern has served as the United States Attorney for the District of Massachusetts, the Chief Legal Counsel to Governor Michael S. Dukakis and the Chief of the Government Bureau in the Massachusetts Attorney General’s office. Dr Joe Wiley, CEO of Amryt Pharma, commented today: "We are very pleased that the Ministry of Health in the Kingdom of Saudi Arabia has approved the reimbursement of Lojuxta® which … Orphan drug designation may allow Amryt to be eligible for a seven-year period of U.S. Marketing exclusivity upon approval of AP103 and a waiver of the Prescription Drug User Fee Act ("PDUFA") filing fees, subject to certain conditions. DUBLIN, Ireland, and Boston MA, December 23, 2020, Amryt (Nasdaq: AMYT, AIM: AMYT), a global, commercial-stage biopharmaceutical company dedicated to developing and commercializing novel therapeutics to treat patients suffering from serious and life-threatening rare diseases, is pleased to announce today that the U.S. Food and Drug Administration ("FDA") has granted orphan drug designation for AP103 for the treatment of Dystrophic Epidermolysis Bullosa ("DEB"). Joe Wiley, CEO of Amryt Pharma, commented: "Receiving an orphan drug designation from the FDA for our gene-therapy candidate, AP103, is a significant development for patients … Contact the source provider Comtex at [email protected]. in Marketing from Trinity College Dublin and has participated in the INSEAD Executive Leadership Programme. Joe Wiley, CEO of Amryt Pharma, commented: “Lomitapide is an important contributor to Amryt’s commercial performance and growth and today’s announcement demonstrates the progress we are … Dr Joe Wiley, CEO of Amryt Pharma, commented today: “We are very excited to report NICE’s approval of Myalepta® which will now give all England and Wales based patients suffering from … Gerry has a PhD in Chemistry, Black belt in Lean/ Quality Systems and most recently became a certified Business Coach. Joe Wiley, CEO, +353 (1) 518 0200, [email protected], Rory Nealon, CFO/COO, +353 (1) 518 0200, [email protected], Edward Mansfield, Shore Capital, NOMAD, +44 (0) 207 468 7906, [email protected], Tim McCarthy, LifeSci Advisors, LLC, +1 (212) 915 2564, [email protected], Amber Fennell, Consilium Strategic Communications, +44 (0) 203 709 5700, [email protected], COMTEX_376701589/2471/2020-12-23T02:00:46. He graduated as a medical doctor from the University of Leiden, Netherlands in 1988 and obtained his Masters of Business Administration in 1992 at the University of Rochester. He has also been a Board Member and Chief Financial Officer of Conduit plc, an Irish directory services provider with operations in Ireland, the UK, Austria and Switzerland, as well as an Associate Director at AIB Capital Markets, a subsidiary of AIB Group plc, the Irish banking group. He has more than 25 years of experience as a successful executive in the pharmaceutical and biotech field on both a national and international scale including specific expertise in rare disease (ACTIMMUNE, RAVICTI, PROCYSBI), autoimmune (HUMIRA), primary care, orthopedic (CELEBREX), diabetes (BYETTA), anti-infectives and cardiovascular spaces. Stern is Managing Director of Corporate Monitoring & Consulting Services at Affiliated Monitors Inc., a consulting firm providing independent integrity monitoring services and compliance services across a wide range of regulated industries and professions. ... now give all England and Wales based patients suffering from lipodystrophy the opportunity to access Myalepta,” said Joe Wiley, chief executive officer of Amryt. He holds a Bachelor of Commerce degree from University College Dublin, is a Fellow of the Institute of Chartered Accountants in Ireland, a member of the Institute of Taxation in Ireland and a member of the Institute of Corporate Treasurers in the UK. The forward-looking statements in this announcement are based on numerous assumptions and Amryt's present and future business strategies and the environment in which Amryt expects to operate in the future. Supreme Court calls emoluments lawsuits against Trump moot, Supreme Court dismisses as moot emoluments suits against Trump, Apple price target gets a boost at Raymond James, ‘I’m tired of being the only one with moral values’: My mother put me on the deed of her home. Joe Wiley is CEO/Co-Founder at Amryt Pharma Ltd. See Joe Wiley's compensation, career history, education, & memberships. The person making this notification on behalf of Amryt is Rory Nealon, CFO/COO and Company Secretary. Dr. Wiley founded Amryt and has over 20 years of experience in the pharmaceutical, medical and venture capital industries. Mr. Allmond was previously Corporate Vice President of Global Marketing at Celgene, where he played a pivotal role in defining strategy for in-line brands, lifecycle/pipeline prioritisation and commercial direction for business development. Many of these risks and uncertainties relate to factors that are beyond each of Amryt's ability to control or estimate precisely, such as future market conditions, the course of the COVID-19 pandemic, currency fluctuations, the behaviour of other market participants, the outcome of clinical trials, the actions of regulators and other factors such as Amryt's ability to obtain financing, changes in the political, social and regulatory framework in which Amryt operates or in economic, technological or consumer trends or conditions. Joe Wiley, CEO of Amryt Pharma, commented:“Receiving an orphan drug designation from the FDA for our gene-therapy candidate, AP103, is a significant development for patients suffering … Dr Mark Sumeray joined Amryt Pharma in September 2016. Metreleptin is also approved for lipodystrophy in Japan. While there, he had clinical development, medical affairs and pharmacovigilance responsibility for the global approval and launch of a new treatment, Lojuxta®▼(lomitapide), for the serious and rare genetic disease, Homozygous Familial Hypercholesterolemia. About AmrytAmryt is a biopharmaceutical company focused on developing and delivering innovative new treatments to help improve the lives of patients with rare and orphan diseases. He is advisor to Kurma Partners and serves on the scientific advisory board of Valneva SA. Prior to joining Currax, Mr. Hampton served as executive vice president, primary care business unit for Horizon Pharmaceuticals (HZNP), a public biopharmaceutical company. Joe Wiley, CEO of Amryt Pharma, commented: "Receiving an orphan drug designation from the FDA for our gene-therapy candidate, AP103, is a significant development for patients … He led the clinical and scientific interactions with global health authorities, including the US Food and Drug Administration. Hampton earned his Bachelor of Science from Miami University in Oxford, Ohio. Website Last updated: 04/01/2021 – Corp/2017/001. Mr.Wills also serves on the boards of: Caliper Corporation, since 2016; MediWound Ltd., since 2017; and Gamida Cell Ltd., since 2019. Her experience has been in multiple sectors in the UK and Republic of Ireland including Construction, Television, Technology and Waste Management. Prior to joining Astellas Pharma Limited, he held investment roles at Spirit Capital SA, Inventages Venture Capital Investment Inc. and Aberdeen Asset Managers Private Equity Limited. Before that, Derval worked for 11 years as a Managing Consultant at Real Regulatory Ltd, a consultancy specialising in European regulatory affairs, quality management systems and supply chain operations compliance. Kieran Rooney joined Amryt Pharma as VP, Strategic Alliances and Licensing, in August 2017. View Joseph Wiley’s profile on LinkedIn, the world’s largest professional community. Mr. Stern holds a Masters in Laws from University of Pennsylvania Law School, a Juris Doctor degree from Georgetown University Law Center and a Bachelor of Arts from Hobart College. Dr. Munoz, M.D., Ph.D. is an entrepreneur and independent management consultant in the pharmaceutical and biotechnology industry, and has over 30 years of experience in the industry at the executive level. Dr. Vink serves as Chairman at Acacia Pharma Group plc and Targovax ASA, both publicly listed biopharma companies based in the UK and Norway. Prior to joining Astellas Pharma Limited, he held investment roles at Spirit Capital SA, Inventages Venture Capital Investment Inc. and Aberdeen Asset Managers Private Equity Limited. Mr. Stern was previously a director of Novelion until September 2019, and previously a member of Aegerion’s board of directors from September 2015 through to October 2016.Mr. Amryt Chief Executive Officer Joe Wiley said the Phase III readout represents an important advancement for patients and families living with EB, a genetic skin disorder that causes the … David Allmond joined Amryt Pharma as Chief Commercial Officer in March 2017. While serving at these companies, Dr. Vink has been involved in initial public listings, geographic expansions and contributed to the achievement of meaningful development and commercial milestones. Dr. Wiley trained in general medicine at Trinity College Dublin, specialising in neurology. Such forward-looking statements reflect the Company's current beliefs and assumptions and are based on information currently available to management. Please confirm you wish to follow this link. AP103 is based on Amryt's gene-therapy platform technology and offers a potential treatment for patients with DEB, a subset of EB. His experience has spanned Supply chain, API, Development, Solid Oral dosage, Semi Solid formulations, Bulk Manufacturing and Aseptic fill finish. Dr. Wiley founded Amryt and has over 20 years of experience in the pharmaceutical, medical and venture capital industries. Mr. Hampton joined Currax Pharmaceuticals in April of 2019 as Chief Executive Officer and serves on its board of directors. Dr. Phillips has over 20 years’ experience in Medical Affairs, working in UK, European and Global roles for AstraZeneca, GSK and Hospira, as well as biotech start-up companies, Aspreva and Vanda. Amryt Granted Orphan Drug Designation by the FDA for AP103. Joseph Wiley is Chief Executive Officer & Executive Director at Amryt Pharma Plc. Mr.Wills served as Executive Chairman and Interim Principal Executive Officer of Derma Sciences, Inc., a public company providing advanced wound care products, from December 2015 until February 2017 when Derma Sciences, Inc. was acquired by Integra LifeSciences Holding Corporation. View Joseph Wiley’s professional profile on Relationship Science, the database of decision makers. Joseph has 9 jobs listed on their profile. Dr Joe Wiley, CEO of Amryt Pharma, commented today: “We are very excited to report NICE’s approval of Myalepta® which will now give all England and Wales based patients suffering from … Dr Joe Wiley, CEO of Amryt Pharma, commented today: “ We are very excited to report NICE’s approval of Myalepta® which will now give all England and Wales based patients suffering from … Most recently Stephen was General Manager, Switzerland at Astellas Pharmaceuticals AG, and prior to that he was Area Marketing & Market Access Director at Astellas Pharma EMEA. A Fellow of the Chartered Institute of Personnel and Development Julie holds a Master’s Degree in Administration and Law. The link you have selected is not under the review or control of Amryt Pharma and, as such, the company does not endorse the content, its accuracy, or any practices or standards contained within it. Dr.Munoz is qualified in cardiology and anaesthesiology from the University Hospital of Montpellier, France where he was head of the clinical cardiology department. He was previously a medical director at Astellas Pharma Limited where he liaised with the marketing team and was involved in the launch of a number of specialty pharmaceutical products. He joined Amryt in February 2019. Dr Joe Wiley, CEO of Amryt Pharma, said the positive outcome of the Phase 3 EASE trial marks another significant milestone for Amryt as it seeks approval for Filsuvez. The MarketWatch News department was not involved in Acquisitions has had a diverse and distinguished career! Ventures Inc Track Designation from the University Hospital of Montpellier, France where he was responsible for marketing... Waste Management Ireland including Construction, Television, Technology and offers a potential treatment for patients DEB. 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