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Arrowhead Pharmaceuticals (ARWR) Presents Interim Data from ARO-ANG3 Phase 2 GATEWAY Study

Arrowhead Pharmaceuticals (ARWR) Presents Interim Data from ARO-ANG3 Phase 2 GATEWAY Study
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Jason bracoBrian ritchieVince anzaloneExchange commissionEuropean atherosclerosis society congressArrowhead pharmaceuticalsLifesci communicationsLifesci advisorsArrowhead pharmaceuticals incDecreases serumAngiopoietin like proteinHomozygous familial hypercholesterolaemiaSan martinHarbor statementPrivate securities litigation reform actAnnual report

Arrowhead Presents Interim Data from ARO-ANG3 Phase 2 GATEWAY Study in Patients with HoFH

- 44-48% Mean Reductions in LDL-C Achieved on Top of Continued Standard of Care - Phase 3 Planning is Ongoing . | May 23, 2023

Arrowhead pharmaceuticalsEuropean atherosclerosis society congressArrowhead pharmaceuticals incDecreases serumAngiopoietin like proteinHomozygous familial hypercholesterolaemiaSan martinHarbor statementPrivate securities litigation reform actNc stock exchangePress releaseS arwr us04280a1007

COMP Adopts Positive Opinion on Orphan Designation for Mycapssa® for the Treatment of Carcinoid Syndrome Associated with Neuroendocrine Tumors

COMP Adopts Positive Opinion on Orphan Designation for Mycapssa® for the Treatment of Carcinoid Syndrome Associated with Neuroendocrine Tumors
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United statesUnited kingdomSaudi arabiaGreat britainRory nealonHypercholesterolaemia hoAmryt pharmaJoe wileyEurope amrytTim mccarthyContactsjoe wileyNational cancer instituteLifesci advisorsCommittee for orphan medicinal productsEuropean unionEuropean medicines agency

European Commission approves Mycapssa® for the treatment of Acromegaly

European Commission approves Mycapssa® for the treatment of Acromegaly Mycapssa® will be the first and only oral somatostatin analog approved in the EU Approval based on MPOWERED Phase 3. | December 5, 2022

United statesUnited kingdomSaudi arabiaGreat britainHypercholesterolaemia hoJoe wileyAmryt pharmaEuropean unionEuropean commissionHomozygous familial hypercholesterolaemiaEpidermolysis bullosaAmryt pharma plc stock exchangePress releaseHase amyt us03217l1061

Amryt Reports Q3 2022 Financial and Operational Results

Amryt Reports Q3 2022 Financial and Operational Results
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United statesUnited kingdomSaudi arabiaGreat britainHypercholesterolaemia hoJoe wileyAmryt reportsAmryt pharmaCompany euroEuropean commissionChiasma incStandard international numberEuropean unionUnited kingdom medical healthcare products regulatory agencyScripts national formulary exclusionAmryt these