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Avista Therapeutics Appoints Steven Altschuler, MD, as Chairman of the Board of Directors

Avista Therapeutics Appoints Steven Altschuler, MD, as Chairman of the Board of Directors

阿維斯塔治療公司任命斯蒂芬·阿爾特舒勒醫生爲董事會主席
PR Newswire ·  01/07 20:15

PITTSBURGH, Jan. 7, 2025 /PRNewswire/ -- Avista Therapeutics, a pre-clinical-stage biotechnology company developing innovative gene therapies for rare ophthalmic conditions, today announced the appointment of Steven Altschuler, MD, as the Chairman of the Board of Directors. Dr. Altschuler brings more than two decades of experience in building and leading world-class translational value-based healthcare systems and innovative biotechnology companies to the Board.

匹茲堡,2025年1月7日/PRNewswire/ -- 阿維斯塔治療公司是一家處於臨牀前階段的生物技術公司,專注於開發創新的基因治療方法以應對罕見的眼科疾病,今天宣佈任命史蒂文·阿爾茨舒勒博士爲董事會主席。阿爾茨舒勒博士在建立和領導世界級的基於價值的醫療保健系統和創新生物技術公司方面擁有超過20年的經驗。

"We are honored to welcome Steve as Chairman of the Board of Directors," said Robert Lin, PhD, Chief Executive Officer of Avista Therapeutics. "With a successful track record as a leader and innovator, coupled with his deep experience in successfully advancing preclinical and clinical gene therapy programs for retinal disease, Steve's expertise and insights will be invaluable as we strive to deliver on our mission of creating next generation gene therapies for blindness."

阿維斯塔治療公司的首席執行官羅伯特·林博士表示:「我們很榮幸歡迎史蒂夫擔任董事會主席。作爲一名成功的領導者和創新者,他在成功推進視網膜疾病的臨牀前和臨牀基因治療項目方面的深厚經驗,將爲我們在致力於開發下一代失明基因治療這一使命的過程中提供寶貴的專業知識和見解。」

Dr. Altschuler serves as Managing Director of Healthcare Ventures at Ziff Capital Partners, leading the firm's efforts in facilitating the startup and development of companies with transformative technologies. He is also the founding CEO and Board Chair of Corner Therapeutics. He previously co-founded Spark Therapeutics and served as Chairman of the Board of Directors, where he played a key role in bringing the first and only FDA-approved retinal gene therapy, LUXTURNA, to market. He formerly held chief executive positions at the University of Miami Health System and Children's Hospital of Philadelphia (CHOP).

阿爾茨舒勒博士擔任Ziff Capital Partners醫療投資的常務董事,領導公司促進具有變革性技術的初創企業的成立和發展。他還是Corner Therapeutics的創始首席執行官和董事會主席。他曾共同創辦Spark Therapeutics,並擔任董事會主席,在那裏他在推進首個也是唯一一個FDA批准的視網膜基因治療LUXTURNA萬億的過程中發揮了關鍵作用。他曾擔任邁阿密大學健康系統和費城兒童醫院(CHOP)的首席執行官。

"The Avista team has developed a potentially paradigm-shifting approach utilizing its scAAVengr platform to improve delivery vectors and broaden gene therapy accessibility beyond sub-retinal delivery," said Dr. Altschuler. "Recently presented preclinical results support the potential of the platform to provide transformative clinical benefit in identifying the most effective viral vectors for delivering gene therapies to the retina. I am excited to collaborate with this talented team to accelerate the development and delivery of life-changing treatments to those affected by retinal diseases."

阿爾茨舒勒博士表示:「阿維斯塔團隊開發了一種潛在的顛覆性方法,利用其scAAVengr平台改善遞送載體,並擴大基因治療超越視網膜下遞送的可及性。最近提出的臨牀前結果支持該平台提供變革性臨牀益處的潛力,以識別最有效的病毒載體,用於將基因治療遞送到視網膜。我很高興能夠與這個優秀的團隊合作,加速對視網膜疾病患者實施改變生活的治療方案的開發和交付。」

Dr. Altschuler is currently on the board of Lexeo Therapeutics, 89Bio, ViaNautis, Innovative Genomic Institute and POLG Foundation. He obtained his MD and BA in mathematics and statistics from Case Western Reserve University. He completed his residency in pediatric medicine at Harvard Medical School and Boston Children's Hospital and his fellowship in gastroenterology and nutrition at the University of Pennsylvania School of Medicine and CHOP.

阿爾茨舒勒博士目前是Lexeo Therapeutics、89bio、ViaNautis、創新基因組研究所和POLG基金會的董事。他從凱斯西儲大學獲得了醫學博士和數學與統計學的學士學位。他在哈佛醫學院和波士頓兒童醫院完成了兒科醫學的住院醫生培訓,並在賓夕法尼亞大學醫學院和兒童醫院完成了胃腸病學與營養的研究員培訓。

About Avista Therapeutics
Avista Therapeutics' mission is to develop innovative gene therapies for retinal diseases, including rare ophthalmic conditions that have a profound impact on patients' quality of life. We leverage our computationally guided scAAVengr platform to generate and validate a toolkit of proprietary AAV vectors that target specific cell types using minimally invasive intravitreal delivery with reduced dosages. Our quantitative, in vivo-based approach and clinical ophthalmology expertise allow us to rapidly translate new gene therapies to the clinic.

關於阿維斯塔治療公司
阿維斯塔治療公司的使命是開發創新的基因療法,以治療視網膜疾病,包括對患者生活質量產生深遠影響的罕見眼科疾病。我們利用計算引導的scAAVengr平台生成和驗證一套專有的AAV載體工具包,針對特定的電芯類型,採用最小侵入性的玻璃體內遞送方式並減少劑量。我們定量的體內基礎方法和臨牀眼科專業知識使我們能夠迅速將新的基因療法轉化爲臨牀應用。

SOURCE Avista Therapeutics

來源:阿維斯塔治療公司

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