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Shire announces submission of lifitegrast Marketing Authorization Application for treatment of dry eye disease in Europe
Director/PDMR Shareholding
Half-yearly Report
Shire reports strong Q2 2017 operating results and cash flow; updates full year guidance
Total Voting Rights
Gap In Perceived and Actual Rates Of Prescription Stimulant Misuse, Abuse and Diversion Found Among College Students
Shire to announce second quarter 2017 results
Shire Expands Broad Monoclonal Antibody Research Platform, Enters License Agreement for Novimmune Bi-specific Antibody
Shire Obtains Injunction Against Roche to Address Incomplete and Misleading Statements Regarding Investigational Agent Emicizumab That May Impact Patient Safety
Additional Listing
Shire submits investigational New Drug Application to FDA for Gene Therapy candidate SHP654 for treatment of Hemophilia A
Shire to present new data at ISTH 2017 to advance the standard of care in Hemophilia
Shire announces EMA validation of VEYVONDI™ [von Willebrand factor (Recombinant)] Marketing Authorization Application for treatment of von Willebrand disease
Director Declaration
U.S. FDA Approves Mydayis™ (mixed salts of a single-entity amphetamine product) – A New Once-Daily Option for ADHD Symptom Control in Patients 13 Years and Older
Shire to participate at the Jefferies healthcare conference
Block listing six monthly return
Shire to highlight new research into chronic hypoparathyroidism at the European Congress of Endocrinology
Shire’s Investigational Treatment Lanadelumab Reduces Hereditary Angioedema Monthly Attack Rate by 87% Versus Placebo in Phase 3 26-week Pivotal Trial
The Lancet Publishes Phase 2 Results from Shire’s Investigational Anti-MAdCAM Antibody Showing Significantly Increased Remission Rates in Patients with Moderate-to-Severe Ulcerative Colitis
Shire Continues 20-Year Commitment to ADHD with New Research at 2017 Annual Meeting of American Psychiatric Association
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