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Vitreoretinal Surgeon and Key Thought Leader Roger Goldberg, M.D., Joins Kiora Pharmaceuticals' Scientific Advisory Board

Vitreoretinal Surgeon and Key Thought Leader Roger Goldberg, M.D., Joins Kiora Pharmaceuticals' Scientific Advisory Board

王震博士,视网膜玻璃体医生兼Kiora药品科学顾问委员会成员
newsfile ·  06/25 06:45

Encinitas, California--(Newsfile Corp. - June 25, 2024) - Kiora Pharmaceuticals (NASDAQ: KPRX) has appointed Roger A. Goldberg, MD, MBA, a vitreoretinal surgeon at Bay Area Retina Associates (BARA) to its Scientific Advisory Board. As an advisor, Dr. Goldberg will contribute scientific insights and valued clinical perspectives to aid Kiora's development of new therapeutics to address retinal diseases with high unmet needs.

加利福尼亚州恩西尼塔斯—(Newsfile Corp. - 2024年6月25日)— Kiora Pharmaceuticals(纳斯达克:KPRX)已任命Bay Area Retina Associates(BARA)的玻璃体视网膜外科医生Roger A. Goldberg,MD,MBA加入其科学咨询委员会。作为顾问,Goldberg博士将提供科学见解和有价值的临床观点,以帮助Kiora开发能够应对严重缺乏治疗方案的视网膜疾病的新型治疗药物。

"As a surgical specialist in retinal disease, my clinical experiences highlight the need for novel and improved treatment options that reverse and/or modify the progression of vision threatening retinal diseases," said Dr. Goldberg. "Kiora's investigational drug, KIO-104, is one example of an asset with this potential given its ability to target overactive immune cells implicated in a wide range of retinal diseases including macular edema, uveitis, and inflammation related vision impairment. I look forward to contributing to Kiora's efforts to advance their technologies so that they may one day benefit as many patients as possible."

“作为视网膜疾病的手术专家,我的临床经验强调了需要新颖和改进的治疗选项,以扭转和/或修改威胁视力的视网膜疾病的进展,”Goldberg医生说道。“Kiora的KIO-104研究药物是具有此潜力的资产之一,因为它能够针对涉及大范围视网膜疾病(包括黄斑水肿,葡萄膜炎和与炎症有关的视力障碍的过度活跃免疫细胞。我期待着为Kiora的技术发展贡献力量,使尽可能多的患者受益。”

Dr. Goldberg has been an investigator in dozens of interventional retinal therapeutic clinical trials. His research has been published extensively including first-author publications in The New England Journal of Medicine, Ophthalmology, JAMA Ophthalmology, and American Journal of Ophthalmology (AJO). He serves as a reviewer for the AJO and Retina, and regularly serves as faculty at national and international meetings. Additionally, Dr. Goldberg co-founded and is currently on the board of directors of Emmecell, a clinical-stage ophthalmic-focused biotechnology company developing regenerative, cell-based therapies for eye diseases.

Goldberg博士参与了数十项干预性视网膜治疗临床试验。他的研究得到了广泛发表,包括在《新英格兰医学杂志》、《眼科学》、《眼科学杂志》和《美国眼科学杂志》(AJO)上的第一作者刊物。他是AJO和Retina的审稿人,并经常在国内外会议上担任教员。此外,Goldberg博士共同创立并目前担任Emmecell的董事会成员,该公司是一家临床阶段的以眼科为重点的生物技术公司,正在开发用于眼部疾病的再生细胞疗法。

Eric Daniels, MD, MBA, Chief Development Officer of Kiora, emphasized the strategic importance of Dr. Goldberg's extensive research background and clinical expertise. "Dr. Goldberg's contributions will enhance our Company's goal to identify and translate innovative treatment options within the ophthalmic field. Retinal inflammation underpins vision loss in a wide range of sight threatening conditions. Starting with KIO-104, Dr. Goldberg's insight will aid in optimizing the development path of a potential first-in-class and clinically practical treatment option for the millions of patients diagnosed with retinal disease globally each year."

Kiora的首席开发官Eric Daniels,MD,MBA强调了Goldberg博士广泛的研究背景和临床专业知识的战略重要性。“Goldberg博士的贡献将增强我们公司的目标,即在眼科领域确定和翻译创新的治疗选择。视网膜炎作为导致多种威胁视力的疾病的基础,从KIO-104开始,Goldberg博士的见解将有助于优化潜在的首创性和临床实用的治疗方案的开发路径,以惠及全球每年被诊断患有视网膜疾病的数百万患者。

Dr. Goldberg graduated from both college and medical school at Yale University. He completed his residency in Miami at the Bascom Palmer Eye Institute, one of the nation's premier eye hospital and residency-training programs. He completed a fellowship in Vitreoretinal Diseases and Surgery at Tufts University and Ophthalmic Consultants of Boston. Dr. Goldberg is board certified by the American Board of Ophthalmology and is an active member of the American Society of Retinal Specialists, the Retina Society, the Association for Research in Vision and Ophthalmology, and the American Academy of Ophthalmology. Dr Goldberg joins the existing members of Kiora's Scientific Advisory Board, including the following key thought leaders:

Goldberg博士在耶鲁大学完成了本科和医学院的学业。他在迈阿密的巴斯克姆帕尔蓝环眼科研究所完成了住院医师培训,该研究所是全国最优秀的眼科医院和住院医师培训项目之一。他曾在Tufts大学和波士顿眼科顾问公司完成了玻璃体视网膜疾病和手术的研究生课程,是美国眼科学会认证的眼科医生,现任美国视网膜专科医师协会、视网膜学会、视觉和眼科行业研究协会和美国眼科学会的活跃会员。Goldberg博士加入了Kiora科学咨询委员会的现有成员,包括以下关键思想领袖:

  • Dr Robert Casson, MD, PhD – Consultant Ophthalmologist at the Royal Adelaide Hospital and Head of the Ophthalmic Research Lab, University of Adelaide.

  • Dr Allen Ho, MD – Attending Vitreoretinal Surgeon and Director of Research at the Wills Eye Hospital, Professor of Ophthalmology at Thomas Jefferson University and partner of Mid Atlantic Retina.

  • Dr Christine Kay, MD, PhD – Inherited Retinal Disease specialist and Vitreoretinal Surgeon at Vitreoretinal Associates in Gainesville, FL and Affiliate Assistant Professor at the University of South Florida.

  • Dr Mark Pennesi, MD, PhD – Inherited Retinal Disease specialist and Director of Ophthalmic Genetics at Retina Foundation of the Southwest.

  • Dr Russell Van Gelder, MD, PhD – Chairman of the Department of Ophthalmology at the University of Washington, and a past president of the American Academy of Ophthalmology.

  • Dr Charles Wykoff, MD, PhD – Vitreoretinal Surgeon and Director of Research at the Retina Consultants of Texas, and Chairman of the Research and Clinical Trials Subcommittee at the Retina Consultants of America.

  • Robert Casson医生,MD,PhD-皇家阿德莱德医院的眼科医生顾问和阿德莱德大学眼科研究实验室主任。

  • Allen Ho医生,MD-威尔斯眼科医院的玻璃体视网膜外科医生和研究主任,托马斯杰斐逊大学眼科学教授,Mid Atlantic Retina的合作伙伴。

  • Christine Kay医生,MD,PhD-位于佛罗里达盖恩斯维尔的Vitreoretinal Associates的遗传性视网膜疾病专家和玻璃体视网膜外科医生,是南佛罗里达大学的联合助理教授。

  • Mark Pennesi医生,MD,PhD-遗传性视网膜疾病专家,并担任西南证券(Retina Foundation of the Southwest)的眼科遗传学主任。

  • Russell Van Gelder医生,MD,PhD-华盛顿大学眼科系主任,美国眼科学会前主席。

  • Charles Wykoff医生,MD,PhD-玻璃体视网膜外科医生,德克萨斯视网膜顾问公司的研究和临床试验小组委员会主席。

About Kiora Pharmaceuticals

关于Kiora Pharmaceuticals

Kiora Pharmaceuticals is a clinical-stage biotechnology company developing and commercializing products for the treatment of orphan retinal diseases. KIO-301 is being developed for the treatment of retinitis pigmentosa, choroideremia, and Stargardt disease. It is a molecular photoswitch that has the potential to restore vision in patients with inherited and/or age-related retinal degeneration. KIO-104 is being developed for the treatment of posterior non-infectious uveitis. It is a next-generation, non-steroidal, immuno-modulatory, and small-molecule inhibitor of dihydroorotate dehydrogenase.

Kiora Pharmaceuticals是一家临床阶段生物技术公司,致力于开发和商业化用于治疗孤儿视网膜疾病的产品。 KIO-301正在开发用于治疗视网膜色素变性症,脉络膜萎缩症和Stargardt病的药物。它是一种有望恢复继发性和/或年龄相关性视网膜变性患者视力的分子光开关。 KIO-104正在开发用于治疗后部非感染性葡萄膜炎。它是下一代非甾体免疫调节剂,小分子脱氢酶酸的抑制剂。

In addition to news releases and SEC filings, we expect to post information on our website () and social media accounts that could be relevant to investors. We encourage investors to follow us on Twitter and LinkedIn as well as to visit our website and/or subscribe to email alerts.

除了新闻发布和SEC文件外,我们还计划在网站()和社交媒体账户上发布可能与投资者相关的信息。我们鼓励投资者关注我们的Twitter和LinkedIn账户,以及访问我们的网站和/或订阅电子邮件提醒。

Forward-Looking Statements

前瞻性声明

Some of the statements in this press release are "forward-looking" and are made pursuant to the safe harbor provision of the Private Securities Litigation Reform Act of 1995. These "forward-looking" statements include statements relating to, among other things, Kiora's ability to execute on development and commercialization efforts and other regulatory or marketing approval efforts pertaining to Kiora's development-stage products, including KIO-104 and KIO-301, as well as the success thereof, with such approvals or success may not be obtained or achieved on a timely basis or at all, the sufficiency of existing cash on hand to fund operations for specific periods, the projected cash runway, and Kiora's plans to further fund development of KIO-104. These statements involve risks and uncertainties that may cause results to differ materially from the statements set forth in this press release, including, among other things, the ability to satisfy the closing conditions related to the offering ,the ability to conduct clinical trials on a timely basis, market and other conditions and certain risk factors described under the heading "Risk Factors" contained in Kiora's Annual Report on Form 10-K filed with the SEC on March 25, 2024 or described in Kiora's other public filings including on Form 10-Q filed with the SEC on May 10, 2024. Kiora's results may also be affected by factors of which Kiora is not currently aware. The forward-looking statements in this press release speak only as of the date of this press release. Kiora expressly disclaims any obligation or undertaking to release publicly any updates or revisions to such statements to reflect any change in its expectations with regard thereto or any changes in the events, conditions, or circumstances on which any such statement is based, except as required by law.

本新闻稿中的某些声明是“前瞻性的”,并根据私人证券诉讼改革法案的安全港条款(1995年)发表。这些“前瞻性”声明包括与Kiora的发展和商业化努力以及有关Kiora的开发阶段产品(包括KIO-104和KIO-301)的其他监管或市场批准努力相关的声明,这种批准或成功可能无法及时获得或实现,现有的现金足以资助特定期间的运营,预期的现金运营期以及Kiora进一步资助KIO-104开发的计划。这些陈述涉及风险和不确定性,可能会导致结果与本新闻稿所述的陈述有所不同,其中包括但不限于如期进行临床试验的能力、市场和其他条件以及描述于2024年3月25日提交给美国证券交易委员会(SEC)的Kiora的《年度报告》(Form 10-K)或描述于2024年5月10日提交给SEC的Kiora的其他公开文件中的某些风险因素,或者Kiora目前不知道的某些因素。本新闻稿中的前瞻性陈述仅适用于本新闻稿的发布日期。Kiora明确否认对任何更新或修订这些陈述以反映其期望或任何基于任何该等陈述依据的事件、情况或情形的义务或承诺,除非受法律要求。

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