Arrowhead Pharmaceuticals
Company type | Public |
---|---|
Industry | Biotechnology |
Founded | 1 January 2004 |
Headquarters | Pasadena, California, U.S. |
Key people | Christopher Anzalone, Ph.D., president and chief executive officer |
Revenue | $243.2 million (2022)[1] |
Number of employees | 376 |
Website | arrowheadpharma |
Arrowhead Pharmaceuticals is a publicly traded biopharmaceutical company based in Pasadena, California. Arrowhead’s products in development act through RNA interference (RNAi) mechanisms of action.[2][3] The company focuses on treatments for hepatitis B, liver disease associated with alpha 1-antitrypsin deficiency and cardiovascular disease.[2]
History
[edit]In 2015, the company substantially expanded its intellectual property holdings through complete acquisition of the full RNAi research and development portfolio, and assets from Novartis.[4][5]
In April 2016, the company announced a name change from Arrowhead Research Corporation to Arrowhead Pharmaceuticals, Inc.[6]
In September 2016, Arrowhead entered into two collaboration and licensing agreements with Amgen. Under the deals, Amgen received a worldwide exclusive license to Arrowhead’s ARO-LPA RNAi program and an option to a worldwide exclusive license for ARO-AMG1, both for cardiovascular disease.[7]
On Oct. 31, 2018, Arrowhead Pharmaceuticals Inc. closed on a $3.7 billion license and collaboration agreement with Janssen to develop and commercialize ARO-HBV. As part of the deal, Arrowhead entered into a research collaboration and option agreement with Janssen to potentially collaborate for up to three more RNA interference (RNAi) therapeutics against new targets to be selected by Janssen.[8]
Products
[edit]The company has sixteen products in its pipeline, in various stages of development.[2]
Product | Indication | Development phase | Notes |
---|---|---|---|
ARO-HBV[2] | Hepatitis B | In clinic, phase 2 | Licensed with Janssen, Phase 2 |
ARO-AAT[2] | Alpha-1 antirypsin deficiency | In clinic, phase 3 | Orphan Drug designation, partnered with Takeda |
ARO-APOC3[2] | Hypertriglyceridemia | Phase 2, 3 | Orphan Drug designation, Fast Track Designation, Phase 3 for FCS, Phase 2 for expanded populations |
ARO-HIF2[2] | Renal cell carcinoma | Preclinical | Second generation being worked on presumably |
ARO-ENaC[2] | Cystic fibrosis | Preclinical | Second generation being worked on in preclinic |
ARO-ANG3[2] | Dyslipidemia | In clinic, Phase 2 | Orphan Drug designation |
Olpasiran/ AMG 890[2] | Cardiovascular disease | In clinic, phase 3 | Partnered with Amgen |
ARO-PNPLA3 | NASH | In clinic, Phase 1 | License returned to ARWR |
ARO-HSD | NASH | In clinic, Phase 1 | Licensed to GSK |
ARO-C3 | Complement Mediated Disease | In clinic, Phase 1 | |
ARO-MUC5AC | Muco-obstructive | In clinic, Phase 1 | |
ARO-RAGE | Inflammatory | In clinic, Phase 1 | |
ARO-MMP7 | Idiopathic Pulmonary Fibrosis | In clinic, Phase 1 | |
ARO-COV | Covid-19 | Preclinical | |
ARO-DUX4 | FSHD | Preclinical | |
HZN-457 | Gout | In clinic, Phase 1 | Partnered with Horizon |
References
[edit]- ^ "Arrowhead Pharmaceuticals Reports Fiscal 2022 Year End Results". November 28, 2022.
- ^ a b c d e f g h i j "arwr-10q_20170331.htm". www.sec.gov. Retrieved 2017-05-17.
- ^ "8-K". www.sec.gov. Retrieved 2017-05-17.
- ^ "Arrowhead buys Novartis' RNAi portfolio". Reuters. 2017-03-05. Retrieved 2017-05-17.
- ^ Staff (1 April 2015). "Novartis Sells RNAi R&D Portfolio to Arrowhead in $35M Agreement". News: Industry Watch. Genetic Engineering & Biotechnology News (Paper). 35 (7): 10.
- ^ "Arrowhead Research Changes Name to Arrowhead Pharmaceuticals". www.businesswire.com. 2016-04-06. Retrieved 2020-04-06.
- ^ "Amgen, Arrowhead team up on gene-therapies for heart disease". Reuters. 2017-09-29. Retrieved 2017-05-17.
- ^ "Arrowhead Enters $3.7 Billion License and Collaboration". Marketwatch. 2018-10-04. Retrieved 2018-10-04.