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Exsilio Therapeutics Launches With $82 Million Series A Financing to Develop Redosable Genomic Medicines for A Broad Range of Diseases

Exsilio Therapeutics Launches With $82 Million Series A Financing to Develop Redosable Genomic Medicines for A Broad Range of Diseases

Exsilio Therapeutics推出8200萬美元的A輪融資,開發針對廣泛疾病的可重複用基因組醫藥。
PR Newswire ·  06/25 17:00

Series A co-led by Novartis Venture Fund and Delos Capital, with participation from OrbiMed, Insight Partners, J.P. Morgan Life Sciences Private Capital, CRISPR Therapeutics, Innovation Endeavors, Invus, Arc Ventures, and Deep Insight

由Novartis Venture Fund和Delos Capital共同領導的A輪融資,OrbiMed,Insight Partners,J.P. Morgan Life Sciences Private Capital,CRISPR Therapeutics,Innovation Endeavors,Invus,Arc Ventures和Deep Insight參與。

Company is developing a new class of genomic medicines based on naturally occurring genetic elements that may be delivered using mRNA and lipid nanoparticles to precisely and durably insert entire genes into safe harbor sites in the human genome

該公司正在開發一種新型基因組藥物,它基於自然遺傳元素,可以使用mRNA和脂質納米粒子精確而持久地插入人類基因組的安全港口位置。

Company is focused on advancing medicines that can be redosed and titrated with curative intent for patients suffering from genetic diseases, cancer, and autoimmune conditions

該公司專注於推進可以紅藥治療遺傳疾病、癌症和自身免疫性疾病的藥物。

BOSTON, June 25, 2024 /PRNewswire/ -- Exsilio Therapeutics ("Exsilio"), a biotechnology company developing genomic medicines for a broad range of diseases, announced today its emergence from stealth with $82 million in Series A financing. The funding was co-led by Novartis Venture Fund and Delos Capital, with participation from OrbiMed, Insight Partners, J.P. Morgan Life Sciences Private Capital, CRISPR Therapeutics, Innovation Endeavors, Invus, Arc Ventures, and Deep Insight. Exsilio was seed-funded by OrbiMed.

馬薩諸塞州波士頓,2024年6月25日/ PRNewswire/--生物技術公司Exsilio Therapeutics(“Exsilio”)宣佈從隱蔽狀態中出現,獲得8200萬美元的A輪融資。這筆資金由Novartis Venture Fund和Delos Capital共同領導,OrbiMed,Insight Partners,J.P. Morgan Life Sciences Private Capital,CRISPR Therapeutics,Innovation Endeavors,Invus,Arc Ventures和Deep Insight參與。Exsilio的種子資金是由OrbiMed提供的。

Tal Zaks, M.D., Ph.D., Exsilio Therapeutics
Tal Zaks,MD,Ph.D.,Exsilio Therapeutics

Exsilio will use proceeds from the financing to advance its genomic medicines based on naturally occurring, programmable genetic elements that can precisely insert new genes into a cell through mRNA intermediates. Exsilio's interdisciplinary team has built a platform that combines predictive in silico modeling and wet lab-based experimentation to discover and engineer such elements for integration of therapeutic genes into safe harbor sites. Because Exsilio's medicines are encoded in mRNA, they can be delivered using existing lipid nanoparticle (LNP) platforms that are safe, efficient, scalable, and cost-effective, and can be redosed and titrated with curative intent.

Exsilio將利用此次融資所得的資金推進其基因組藥物的發展,該藥物基於具有可編程遺傳元素的自然發生物,可以通過mRNA中介精確地插入新基因到細胞中。Exsilio的跨學科團隊構建了一個平台,將預測性的硅建模與基於實驗的溼實驗相結合,以發現和設計用於將治療基因整合到安全海港位點中的此類型元素。因爲Exsilio的藥物是通過mRNA編碼的,所以它們可以使用現有的脂質納米粒子(LNP)平台進行傳遞,這些平台是安全、高效、可擴展和具有成本效益的,並且可以通過持久的紅劑量進行調整。

"mRNA-based medicines allow for a software-like approach to creating new medicines," said Tal Zaks, M.D., Ph.D., who serves as Exsilio's Chairman and Interim Chief Executive Officer. "Exsilio's approach leverages the advantages of mRNA and goes a step further by encoding genes that integrate permanently, offering the possibility of curative rather than transient effects. The ability to insert whole genes with a repeatable and titratable approach should allow us to treat genetic diseases irrespective of the patient's individual mutation. This financing will help us advance our genomic medicines and select promising lead candidates so that we can bring much-needed new options to patients."

“mRNA藥物能夠實現類似於軟件的方法來創建新藥物,”Exsilio的董事長兼代行首席執行官Tal Zaks,MD,Ph.D.,說道。 “Exsilio的方法利用了mRNA的優勢,並進一步編碼了整個基因,提供了治癒而不是短暫效果的可能性。通過可以反覆使用、可進行定量的方法插入整個基因,應該能夠治療遺傳疾病,無論患者的個體突變如何。這筆融資將幫助我們推進我們的基因組藥物,選擇有前途的首席候選人,這樣我們就可以爲患者帶來急需的新選擇。”

"We were captivated by Exsilio's genomic medicines approach that stands to enable large-gene integration in a safe and redosable manner," said Aaron Nelson, Managing Director at Novartis Venture Fund and Exsilio Board Member. "Through this significant investment, Exsilio will be able to select and advance promising candidates for difficult-to-treat diseases."

“我們被Exsilio的基因組藥物方法所吸引,這種方法可以在安全可體量的情況下啓用大的基因整合和到期劑量的可重複和可紅罰款的方式,“Novartis Venture Fund的管理董事Aaron Nelson說,他同時是Exsilio董事會成員。“通過這筆重大投資,Exsilio將能夠選擇和推進難治性疾病的有前途的候選人。“

"We believe that the vision of safely and durably integrating therapeutic genes into a patient's genome requires using RNA-based payloads that can leverage clinically validated non-viral gene delivery technologies," said Henry Chen, Managing Partner of Delos Capital and Exsilio Board Member. "Exsilio is bringing together a singular group of people to help establish this new pillar of genomic medicine."

“我們相信,將治療基因安全耐久地整合到患者的基因組中的願景需要使用RNA爲基礎的載荷,這些載荷可以利用臨床驗證的非病毒基因遞送技術,”Delos Capital的合夥人Henry Chen說道,並擔任Exsilio董事會成員。“Exsilio正在彙集一群人,幫助建立這種基礎基因組醫學的新支柱。“

About Exsilio Therapeutics
Exsilio Therapeutics is developing genomic medicines that can be delivered in lipid nanoparticles to durably and safely treat a broad range of diseases, including genetic diseases, cancer, and autoimmune conditions. Exsilio's technology is based on naturally occurring genetic elements that can precisely insert new genes into a cell through RNA intermediate templates. Exsilio uses predictive in silico modeling and wet lab-based experimentation to engineer such elements for precise insertion of therapeutic genes into safe harbor sites of disease-relevant cells. Because Exsilio's medicines are encoded in mRNA, they can be delivered using validated, non-viral delivery platforms that are safe, efficient, scalable, and cost-effective, and that allow redosing to effect with a curative intent. For more information, follow us on LinkedIn.

關於Exsilio Therapeutics
Exsilio Therapeutics正在開發可以通過脂質納米粒子持久而安全地治療各種疾病的基因組藥物,包括遺傳性疾病、癌症和自身免疫性疾病。Exsilio的技術基於可通過RNA中介模板將新基因精確插入細胞中的自然發生遺傳元素。 Exsilio利用預測性的硅建模和基於實驗的溼實驗來設計此類元素,以便將治療性基因精確定位到與該疾病相關的細胞的安全海港位點。由於Exsilio的藥物是通過mRNA編碼的,因此它們可以使用驗證的非病毒遞送平台進行傳遞,這些平台安全,高效,可擴展且成本效益,並且可以使用紅劑量進行治療。如需更多信息,請關注我們的Linkedin。

SOURCE Exsilio

來源Exsilio

譯文內容由第三人軟體翻譯。


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