Arrowhead Pharmaceuticals to Participate in Upcoming December 2024 Conferences
ARWR 12.02.2024
Drug:Plozasiran-UNKNOWN Plozasiran
Diseases:Familial Chylomicronemia Syndrome
Date of Upcoming Event:2024-12-03
Name of Upcoming Event:Piper Sandler 36th Annual Healthcare Conference
Date of Upcoming Event:2024-12-04
Name of Upcoming Event:7th Annual Evercore ISI HealthCONx Conference
Date of Upcoming Event:2024-12-09
Name of Upcoming Event:The APA/JPS/CAP/IAP 2024 Joint Meeting
Date of Upcoming Event:2024-12-09
Name of Upcoming Event:RNA at the Bench and Bedside IV
Date of Upcoming Event:2024-12-10
Name of Upcoming Event:21st Global CVCT Forum
Date of Upcoming Event:2024-12-11
Name of Upcoming Event:8th Complement-Based Drug Development Summit
Date of Upcoming Event:2024-12-13
Name of Upcoming Event:22nd World Congress on Insulin Resistance, Diabetes & Cardiovascular Disease (WCIRDC)

About Gravity Analytica
Recent News
- 02.10.2025 - Arrowhead Pharmaceuticals 2025 First Quarter Results
- 01.22.2025 - Arrowhead Pharmaceuticals to Webcast Fiscal 2025 First Quarter Results
- 01.17.2025 - Arrowhead Pharmaceuticals Announces Acceptance of New Drug Application by U.S. FDA of Plozasiran for the Treatment of Familial Chylomicronemia Syndrome
Recent Filings
Piper Sandler 36th Annual Healthcare Conference –
Type: Fireside Chat PresentationDate/Time:
7thAnnual
Type: Fireside Chat PresentationDate/Time:
The APA/JPS/CAP/IAP 2024 Joint Meeting –
Title:PALISADE: A Phase 3 Study to Assess the Efficacy and Safety of Plozasiran in adults with Genetically or Clinically-Defined Familial Chylomicronemia Syndrome (FCS) at high risk of Acute Pancreatitis (AP)Date/Time:
RNA at the Bench and Bedside IV –
Title:Developing siRNA for Neurodegenerative DisordersDate/Time:
21st
Title:A Randomized, Placebo-Controlled Phase 3 Study of Plozasiran in Patients with Familial Chylomicronemia SyndromeDate/Time:
8thComplement-Based Drug Development Summit –
Title:Targeting Complement C3 and Factor B with siRNA: Concept to ClinicDate/Time:
22nd
Title:PALISADE: A Phase 3 Study to Assess the Efficacy and Safety of Plozasiran in Adults with Genetically or Clinically-Defined Familial Chylomicronemia Syndrome (FCS) at high risk of Acute Pancreatitis (AP)Date/Time:
Presentation materials may be accessed on theEvents and Presentationspage under the Investors section of the Arrowhead website.
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This news release contains forward-looking statements within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. Any statements contained in this release except for historical information may be deemed to be forward-looking statements. Without limiting the generality of the foregoing, words such as “may,” “will,” “expect,” “believe,” “anticipate,” “hope,” “intend,” “plan,” “project,” “could,” “estimate,” “continue,” “target,” “forecast” or “continue” or the negative of these words or other variations thereof or comparable terminology are intended to identify such forward-looking statements. In addition, any statements that refer to projections of our future financial performance, trends in our business, expectations for our product pipeline or product candidates, including anticipated regulatory submissions and clinical program results, prospects or benefits of our collaborations with other companies, or other characterizations of future events or circumstances are forward-looking statements. These forward-looking statements include, but are not limited to, statements about the initiation, timing, progress and results of our preclinical studies and clinical trials, and our research and development programs; our expectations regarding the potential benefits of the partnership, licensing and/or collaboration arrangements and other strategic arrangements and transactions we have entered into or may enter into in the future; our beliefs and expectations regarding milestone, royalty or other payments that could be due to or from third parties under existing agreements; and our estimates regarding future revenues, research and development expenses, capital requirements and payments to third parties. These statements are based upon our current expectations and speak only as of the date hereof. Our actual results may differ materially and adversely from those expressed in any forward-looking statements as a result of numerous factors and uncertainties, including the impact of the ongoing COVID-19 pandemic on our business, the safety and efficacy of our product candidates, decisions of regulatory authorities and the timing thereof, the duration and impact of regulatory delays in our clinical programs, our ability to finance our operations, the likelihood and timing of the receipt of future milestone and licensing fees, the future success of our scientific studies, our ability to successfully develop and commercialize drug candidates, the timing for starting and completing clinical trials, rapid technological change in our markets, the enforcement of our intellectual property rights, and the other risks and uncertainties described in our most recent Annual Report on Form 10-K, subsequent Quarterly Reports on Form 10-Q and other documents filed with the
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