Press release

Arrowhead Pharmaceuticals Reports Fiscal 2022 First Quarter Results

- Conference Call and Webcast Today, February 2, 2022 at 4:30 p.m. ET PASADENA, Calif.--(BUSINESS WIRE)-- Arrowhead Pharmaceuticals, Inc. (NASDAQ: ARWR)

articleArrowhead Pharmaceuticals, Inc.February 2, 20223/company/arrowhead-pharmaceuticals-inc/news/arrowhead-pharmaceuticals-reports-fiscal-2022-first-quarter-results-2022-02-02
Arrowhead Pharmaceuticals Reports Fiscal 2022 First Quarter Results

About this update from Arrowhead Pharmaceuticals, Inc.

[{"type":"text","content":"\n- Conference Call and Webcast Today, February 2, 2022 at 4:30 p.m. ET\n\n PASADENA, Calif.--(BUSINESS WIRE)--\nArrowhead Pharmaceuticals, Inc. (NASDAQ: ARWR) today announced financial results for its fiscal first quarter ended December 31, 2021. The company is hosting a conference call today, February 2, 2022, at 4:30 p.m. ET to discuss the results.\n\nConference Call and Webcast Details\n\nInvestors may access a live audio webcast on the Company's website at http://ir.arrowheadpharma.com/events.cfm. For analysts that wish to participate in the conference call, please dial 855-215-6159 or 315-625-6887 and provide Conference ID 9844328.\n\nA replay of the webcast will be available on the company’s website approximately two hours after the conclusion of the call and will remain available for 90 days. An audio replay will also be available approximately two hours after the conclusion of the call and will be available for 3 days. To access the audio replay, dial 855-859-2056 or 404-537-3406 and provide Conference ID 9844328.\n\nSelected Recent Events\n\n\nInitiated the PALISADE Phase 3 clinical study to evaluate the efficacy and safety of ARO-APOC3, Arrowhead’s investigational RNA interference (RNAi) therapeutic designed to inhibit the production of apolipoprotein C-III (APOC3), a key regulator of triglyceride metabolism, in adults with familial chylomicronemia syndrome\n\n\nAdvanced two new investigational candidates that utilize Arrowhead’s pulmonary targeted TRiMTM platform into CTA enabling studies with both on track to file CTAs in the first half of 2022. Both candidates are designed to treat various muco-obstructive and inflammatory pulmonary conditions\n\n\nARO-RAGE, an investigational RNAi therapeutic designed to inhibit the production of Receptor for Advanced Glycation End products (RAGE)\n\n\nARO-MUC5AC, an investigational RNAi therapeutic designed to inhibit the production of mucin 5AC (MUC5AC)\n\n\n\n\nCompleted a transaction to purchase 13 acres of land in the Verona Technology Park in Verona, WI, which is planned to be the site of an approximately 140,000 square foot drug manufacturing facility and an approximately 115,000 square foot laboratory and office facility to support process development and analytical activities\n\n\nEntered into an exclusive license agreement with GlaxoSmithKline (GSK) under which GSK will ...

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