Arrowhead Pharmaceuticals Refinances Existing Credit Facility
Arrowhead Pharmaceuticals has completed a refinancing of its $400 million credit facility with Sixth Street, reducing borrowing costs and extending debt maturity.
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Arrowhead Reports First Clinical Validation Of TRiM Platform As ARO-MAPT Achieves Up To 73% Mean and 85% Maximum Tau Reduction
Arrowhead’s TRiM™ platform achieves clinical validation for delivery of siRNA that crosses the blood-brain barrier after subcutaneous injectionARO-MAPT demonstrates mean cerebrospinal fluid total tau reduction of 73% on
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8-K filing — ARROWHEAD PHARMACEUTICALS, INC. (ARWR)
Filed: 2026-11-04 AccNo: 0000879407-26-000063 Size: 258 KB Item 1.01: Entry into a Material Definitive Agreement Item 2.03: Creation of a Direct Financial Obligation or an Obligation under an Off-Balance Sheet Arrangement of a Registrant
Arrowhead Pharmaceuticals to Webcast 2026 Fiscal Year-End Results
Arrowhead Pharmaceuticals, Inc. announced it will host a conference call and webcast on November 12, 2026, to discuss its financial results for the fiscal year ended September 30, 2026.
Arrowhead Pharmaceuticals to Present Clinical Data on ARO-DIMER-PA at AHA Scientific Sessions 2026
Arrowhead Pharmaceuticals announced it will present first-in-human trial data for its dual-functional RNAi molecule, ARO-DIMER-PA, at the American Heart Association Scientific Sessions 2026.
Arrowhead Pharmaceuticals Receives UK Marketing Authorisation for REDEMPLO
The UK's Medicines and Healthcare products Regulatory Agency (MHRA) has granted marketing authorisation for REDEMPLO (plozasiran) to treat adults with Familial Chylomicronaemia Syndrome (FCS).
Arrowhead Pharmaceuticals Announces REDEMPLO (plozasiran) Availability in England and Wales
Arrowhead Pharmaceuticals announced that REDEMPLO (plozasiran) is now available on the NHS for adults in England and Wales with Familial Chylomicronaemia Syndrome (FCS).