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Industry | |
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Founded | 2003 |
Fate | Acquired by Roche Pharmaceuticals |
Headquarters | Copenhagen, Denmark |
Products | RNA-targeted medicines, Locked nucleic acid (LNA) based drugs |
Santaris Pharma A/S was a biopharmaceutical company founded in 2003 in Copenhagen, Denmark. [1] The company also had a branch in San Diego, California that opened in 2009. [2] Created by a merger between Cureon and Pantheco, Santaris developed RNA-targeted medicines using a Locked Nucleic Acid (LNA) Drug Platform and Drug Development Engine. [3]
Santaris had gained intellectual property rights to the therapeutic applications of locked nucleic acid (LNA) technology. These rights included ownership of several patents, mostly with the chemistry and manufacturing of therapeutic drugs. With its LNA technology, Santaris developed drugs for the treatment of cancers and tumours using microRNA and mRNA. Its research focused on infectious diseases and metabolic disorders. The company also worked on collaborations with other pharmaceutical companies to develop drugs that could treat cancers and rare genetic disorders, among other things. [3]
In August 2014, Santaris was acquired by Roche for $450 million. As a result, the Copenhagen site was renamed the Roche Innovation Center Copenhagen (RICC). [4] RICC houses Roche's RNA Molecule Research, which is part of Roche Pharma Research and Early Development. [5] In 2023, it was closed due to a decision to move research to Basel, Switzerland where Roche is headquartered. [6] The former employees of the RICC were offered new jobs at the Danish pharmaceutical company Novo Nordisk. [7]
Santaris developed drugs based on Locked nucleic acid (LNA) to facilitate the identification and design of potential drug candidates. LNA oligonucleotides were engineered by Santaris as antisense therapeutic agents, designed to complement specific mRNA and microRNA sequences. This interaction leads to the formation of double-stranded RNA, preventing translation. Notably, LNA oligonucleotides are shorter than other antisense drugs, granting them greater target affinity and potency compared to regular RNA oligonucleotides.
One of the distinctive qualities of LNA drugs is their resistance to endonuclease activity, which contributes to their durability. Moreover, LNA drugs possess other advantageous attributes in comparison to other therapeutic agents: they can be administered without the need for complex drug delivery methods, their production is scalable and cost-effective, they are well-tolerated.[ verification needed] These factors collectively define LNA-based drugs as innovative therapeutic agents. [8] [9] [3]
In 2009, Santaris announced that two LNA based drugs EZN-3042, and EZN-2968 would be entering clinical trials. [10] EZN-2968 is an inhibitor of a transcription factor, specificially HIF-1 alpha, which is involved in cells ability to undergo angiogenesis and other processes needed for cell survival. EZN-3042 is also an inhibitor, which acts against Survivin. Santaris partnered with Enzon Pharmaceuticals, [11] for the development of both drug candidates.
SPC-4955 was a drug intended for the treatment of high cholesterol. SPC-4955 inhibits the protein that is necessary for the formation of plasma LDL cholesterol particles. This has the potential to be used as a treatment for patients with hyperlipidemia. [12] SPC-5001 which targets PCSK9 program also has the potential to treat patients with hyperlipidemia. It inhibits the protein that controls the number of receptors responsible for removing LDL cholesterol particles from the blood. [12]
As of 2022, clinical trials on SPC-4955 have been discontinued by Roche. [13]
Santaris developed a microRNA targeting drug for hepatitis C (HCV), miravirsen (SPC3649), [14] which entered Phase II clinical trials in 2010. [15] The drug targets miR-122, a host factor necessary for viral replication of the hepatitis C virus in host liver cells; because miravirsen targets a host factor rather than the virus itself, there are no indications of the virus developing resistance. [16] [ citation needed] The U.S. Food and Drug Administration approved a multiple dosing study, by injection, to treatment-naive patients for phase II testing. [15]
Santaris had a collaboration with Shire to discover and develop new RNA-based medicines to treat rare genetic disorders. [17]
Santaris partnered with several pharmaceutical companies that wanted to develop LNA oligonucleotides for mRNA and microRNA targets. Pfizer and Santaris entered a collaboration pact in 2009, which was expanded in 2011. [18] It also had a partnership with Enzon for cancer drug targets, [11] Shire for lead candidates of five rare, undisclosed genetic disorders, [17] miRagen to develop treatments targeting microRNAs associated with cardiovascular disease, [19] and GlaxoSmithKline for RNA-targeted medication. [20]
In 2010, Exiqon completed its litigation against Santaris for the supply of LNA. The court determined that both companies may supply the product for research and development of pharmaceutical products. Exiqon was made to pay partial costs to Santaris of DKK 2 million within two weeks. [33]
Isis Pharmaceuticals filed a patent infringement lawsuit against Santaris Pharma A/S in the United States District Court for the Southern District of California in September 2011. Isis's infringement suit against Santaris is based upon Santaris's activities providing antisense drugs and antisense drug discovery services to several pharmaceutical companies. [34]
{{
cite journal}}
: CS1 maint: multiple names: authors list (
link)
![]() | This article has multiple issues. Please help
improve it or discuss these issues on the
talk page. (
Learn how and when to remove these template messages)
|
![]() | |
Industry | |
---|---|
Founded | 2003 |
Fate | Acquired by Roche Pharmaceuticals |
Headquarters | Copenhagen, Denmark |
Products | RNA-targeted medicines, Locked nucleic acid (LNA) based drugs |
Santaris Pharma A/S was a biopharmaceutical company founded in 2003 in Copenhagen, Denmark. [1] The company also had a branch in San Diego, California that opened in 2009. [2] Created by a merger between Cureon and Pantheco, Santaris developed RNA-targeted medicines using a Locked Nucleic Acid (LNA) Drug Platform and Drug Development Engine. [3]
Santaris had gained intellectual property rights to the therapeutic applications of locked nucleic acid (LNA) technology. These rights included ownership of several patents, mostly with the chemistry and manufacturing of therapeutic drugs. With its LNA technology, Santaris developed drugs for the treatment of cancers and tumours using microRNA and mRNA. Its research focused on infectious diseases and metabolic disorders. The company also worked on collaborations with other pharmaceutical companies to develop drugs that could treat cancers and rare genetic disorders, among other things. [3]
In August 2014, Santaris was acquired by Roche for $450 million. As a result, the Copenhagen site was renamed the Roche Innovation Center Copenhagen (RICC). [4] RICC houses Roche's RNA Molecule Research, which is part of Roche Pharma Research and Early Development. [5] In 2023, it was closed due to a decision to move research to Basel, Switzerland where Roche is headquartered. [6] The former employees of the RICC were offered new jobs at the Danish pharmaceutical company Novo Nordisk. [7]
Santaris developed drugs based on Locked nucleic acid (LNA) to facilitate the identification and design of potential drug candidates. LNA oligonucleotides were engineered by Santaris as antisense therapeutic agents, designed to complement specific mRNA and microRNA sequences. This interaction leads to the formation of double-stranded RNA, preventing translation. Notably, LNA oligonucleotides are shorter than other antisense drugs, granting them greater target affinity and potency compared to regular RNA oligonucleotides.
One of the distinctive qualities of LNA drugs is their resistance to endonuclease activity, which contributes to their durability. Moreover, LNA drugs possess other advantageous attributes in comparison to other therapeutic agents: they can be administered without the need for complex drug delivery methods, their production is scalable and cost-effective, they are well-tolerated.[ verification needed] These factors collectively define LNA-based drugs as innovative therapeutic agents. [8] [9] [3]
In 2009, Santaris announced that two LNA based drugs EZN-3042, and EZN-2968 would be entering clinical trials. [10] EZN-2968 is an inhibitor of a transcription factor, specificially HIF-1 alpha, which is involved in cells ability to undergo angiogenesis and other processes needed for cell survival. EZN-3042 is also an inhibitor, which acts against Survivin. Santaris partnered with Enzon Pharmaceuticals, [11] for the development of both drug candidates.
SPC-4955 was a drug intended for the treatment of high cholesterol. SPC-4955 inhibits the protein that is necessary for the formation of plasma LDL cholesterol particles. This has the potential to be used as a treatment for patients with hyperlipidemia. [12] SPC-5001 which targets PCSK9 program also has the potential to treat patients with hyperlipidemia. It inhibits the protein that controls the number of receptors responsible for removing LDL cholesterol particles from the blood. [12]
As of 2022, clinical trials on SPC-4955 have been discontinued by Roche. [13]
Santaris developed a microRNA targeting drug for hepatitis C (HCV), miravirsen (SPC3649), [14] which entered Phase II clinical trials in 2010. [15] The drug targets miR-122, a host factor necessary for viral replication of the hepatitis C virus in host liver cells; because miravirsen targets a host factor rather than the virus itself, there are no indications of the virus developing resistance. [16] [ citation needed] The U.S. Food and Drug Administration approved a multiple dosing study, by injection, to treatment-naive patients for phase II testing. [15]
Santaris had a collaboration with Shire to discover and develop new RNA-based medicines to treat rare genetic disorders. [17]
Santaris partnered with several pharmaceutical companies that wanted to develop LNA oligonucleotides for mRNA and microRNA targets. Pfizer and Santaris entered a collaboration pact in 2009, which was expanded in 2011. [18] It also had a partnership with Enzon for cancer drug targets, [11] Shire for lead candidates of five rare, undisclosed genetic disorders, [17] miRagen to develop treatments targeting microRNAs associated with cardiovascular disease, [19] and GlaxoSmithKline for RNA-targeted medication. [20]
In 2010, Exiqon completed its litigation against Santaris for the supply of LNA. The court determined that both companies may supply the product for research and development of pharmaceutical products. Exiqon was made to pay partial costs to Santaris of DKK 2 million within two weeks. [33]
Isis Pharmaceuticals filed a patent infringement lawsuit against Santaris Pharma A/S in the United States District Court for the Southern District of California in September 2011. Isis's infringement suit against Santaris is based upon Santaris's activities providing antisense drugs and antisense drug discovery services to several pharmaceutical companies. [34]
{{
cite journal}}
: CS1 maint: multiple names: authors list (
link)