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Ocugen Announces CSO to Present on Modifier Gene Therapy At International Society for Cell & Gene Therapy 2024

Ocugen Announces CSO to Present on Modifier Gene Therapy At International Society for Cell & Gene Therapy 2024

Ocugen 宣布 CSO 将在 2024 年国际细胞与基因疗法学会上发表关于改性基因疗法的演讲
Ocugen ·  05/20 00:00

MALVERN, Pa., May 20, 2024 (GLOBE NEWSWIRE) -- Ocugen, Inc. (Ocugen or the Company) (NASDAQ: OCGN), a biotechnology company focused on discovering, developing, and commercializing novel gene and cell therapies and vaccines, today announced that Arun Upadhyay, PhD, Chief Scientific Officer, Head of Research & Development, Ocugen will speak at the International Society for Cell & Gene Therapy (ISCT) Annual Meeting being held May 29-June 1, 2024 in Vancouver, Canada.

宾夕法尼亚州马尔文,2024年5月20日(GLOBE NEWSWIRE)——专注于发现、开发和商业化新型基因和细胞疗法及疫苗的生物技术公司Ocugen公司(Ocugen或公司)(纳斯达克股票代码:OCGN)今天宣布,奥库根首席科学官兼研发主管阿伦·乌帕迪亚博士将在国际细胞与基因疗法学会发表演讲 (ISCT) 年会将于 2024 年 5 月 29 日至 6 月 1 日在加拿大温哥华举行。

"I'm very pleased to present OCU400 data among an organization dedicated to translating cell and gene therapies into safe and effective treatments to improve patients' lives," said Dr. Upadhyay. "OCU400 modifier gene therapy represents a breakthrough approach for the potential treatment of broader retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA) diseases where more than 100 mutations are involved."

Upadhyay博士说:“我很高兴向一个致力于将细胞和基因疗法转化为安全有效的治疗以改善患者生活的组织提供 OCU400 数据。”“OCU400 修饰基因疗法是潜在治疗更广泛的色素性视网膜炎(RP)和莱伯先天性黑蒙症(LCA)疾病的突破性方法,这两种疾病涉及 100 多个突变。”

ISCT provides cutting-edge translational content and an opportunity to connect with global experts from academic institutions, regulatory agencies, and the healthcare industry. Attendees can participate in robust debates, collaborate on developing solutions to sector challenges, and join conversations advancing the field of cell and gene therapy.

ISCT 提供尖端的翻译内容,并有机会与来自学术机构、监管机构和医疗保健行业的全球专家建立联系。与会者可以参与激烈的辩论,合作开发应对行业挑战的解决方案,并参与推进细胞和基因疗法领域的对话。

Details on Dr. Upadhyay's presentation are as follows:

Upadhyay博士的演讲详情如下:

Late-Breaking Oral Abstract Session: Safety and Efficacy Results from a Phase 1/2 Clinical Trial of OCU400 Modifier Gene Therapy for Treatment of Retinitis Pigmentosa

最新口头摘要会议:用于治疗色素性视网膜炎的 OCU400 修饰基因疗法的 1/2 期临床试验的安全性和有效性结果

Date: Thursday, May 30, 2024
Time: 5-6 p.m. PDT
Location: Room 202-204, Vancouver Convention Centre, West Building

日期:2024 年 5 月 30 日星期四
时间:太平洋夏令时间下午 5 点至 6 点
地点:温哥华会议中心西楼202-204室

Dr. Upadhyay's poster will also be available during Poster Networking Session #1 on Wednesday, May 29, 2024 from 7-8:30 p.m. PDT.

Upadhyay博士的海报也将在太平洋夏令时间2024年5月29日星期三晚上7点至8点30分的海报社交会议 #1 期间公布。

The OCU400 Phase 3 liMeliGhT clinical trial is currently underway and on track to meet the Company's 2026 BLA and MAA approval targets. OCU400 is the first gene therapy program to enter Phase 3 with a broad RP indication.

OCU400 三期 LimeLight 临床试验目前正在进行中,有望实现公司 2026 年 BLA 和 MAA 的批准目标。OCU400 是第一个进入第 3 阶段且具有广泛的 RP 适应症的基因治疗计划。

About OCU400
OCU400 is the Company's gene-agnostic modifier gene therapy product based on nuclear hormone receptor (NHR) gene, NR2E3. NR2E3 regulates diverse physiological functions within the retina—such as photoreceptor development and maintenance, metabolism, phototransduction, inflammation and cell survival networks. Through its drive functionality, OCU400 resets altered/affected cellular gene networks and establishes homeostasis—a state of balance, which has the potential to improve retinal health and function in patients with RP. Nearly 300,000 people are affected by RP in the U.S. and EU combined.

关于 OCU400
OCU400 是该公司基于核激素受体 (NHR) 基因的基因无关修饰基因疗法产品, NR2E3NR2E3 调节视网膜内的各种生理功能,例如感光器发育和维持、新陈代谢、光转导、炎症和细胞存活网络。通过其驱动功能,OCU400 重置改变/受影响的细胞基因网络并建立动态平衡状态,这种平衡状态有可能改善 RP 患者的视网膜健康和功能。在美国和欧盟,总共有近30万人受到RP的影响。

About Modifier Gene Therapy
Modifier gene therapy is designed to fulfill unmet medical needs related to retinal diseases, including IRDs, such as RP, LCA and Stargardt disease, as well as multifactorial diseases like dry age-related macular degeneration (dAMD). Our modifier gene therapy platform is based on the use of NHRs, master gene regulators, which have the potential to restore homeostasis — the basic biological processes in the retina. Unlike single-gene replacement therapies, which only target one genetic mutation, we believe that our modifier gene therapy platform, through its use of NHRs, represents a novel approach that has the potential to address multiple retinal diseases caused by mutations in multiple genes with one product, and to address complex diseases that are potentially caused by imbalances in multiple gene networks. Currently, Ocugen has three modifier gene therapy programs in the clinic: OCU400, OCU410, and OCU410ST. In addition to the OCU400 Phase 3 liMeliGhT clinical trial, the OCU410 Phase 1/2 ArMaDa clinical trial for geographic atrophy (GA) secondary to dAMD and the OCU410ST Phase 1/2 GARDian clinical trial for Stargardt disease are currently underway. GA affects approximately two to three million people in the U.S. and EU combined and Stargardt disease affects nearly 100,000 people in the U.S. and EU combined.

关于修饰基因疗法
修饰基因疗法旨在满足与视网膜疾病相关的未满足的医疗需求,包括IRD,例如RP、LCA和Stargardt病,以及干性年龄相关性黄斑变性(dAMD)等多因素疾病。我们的修饰基因疗法平台基于主基因调节剂NHR的使用,它有可能恢复动态平衡——视网膜中的基本生物学过程。与仅针对一种基因突变的单基因替代疗法不同,我们认为,我们的修饰基因疗法平台通过使用NHR,代表了一种新方法,有可能使用一种产品解决由多个基因突变引起的多种视网膜疾病,并解决可能由多个基因网络失衡引起的复杂疾病。目前,Ocugen在临床上有三个修饰基因疗法项目:OCU400、OCU410 和 OCU410ST。除了 OCU400 三期 LimeLight 临床试验外,针对继发于 dAMD 的地理萎缩 (GA) 的 OCU410 1/2 期 Armada 临床试验和针对 Stargardt 病的 OCU410ST 1/2 期 Gardian 临床试验目前正在进行中。在美国和欧盟,GA共影响约200万至300万人,Stargardt病共影响美国和欧盟的近10万人。

About Ocugen, Inc.

关于 Ocugen, Inc.

Ocugen, Inc. is a biotechnology company focused on discovering, developing, and commercializing novel gene and cell therapies and vaccines that improve health and offer hope for patients across the globe. We are making an impact on patient's lives through courageous innovation—forging new scientific paths that harness our unique intellectual and human capital. Our breakthrough modifier gene therapy platform has the potential to treat multiple retinal diseases with a single product, and we are advancing research in infectious diseases to support public health and orthopedic diseases to address unmet medical needs. Discover more at www.ocugen.com and follow us on X and LinkedIn.

Ocugen, Inc. 是一家生物技术公司,专注于发现、开发和商业化能够改善健康并为全球患者带来希望的新型基因和细胞疗法和疫苗。我们正在通过勇敢的创新对患者的生活产生影响——开辟新的科学道路,利用我们独特的智力和人力资本。我们的突破性修饰基因疗法平台有可能用单一产品治疗多种视网膜疾病,我们正在推进传染病研究,以支持公共卫生和骨科疾病,以满足未得到满足的医疗需求。在以下网址了解更多 www.ocugen.com 然后关注我们 X领英

Cautionary Note on Forward-Looking Statements
This press release contains forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995, including, but not limited to, statements regarding qualitative assessments of available data, potential benefits, expectations for ongoing clinical trials, anticipated regulatory filings and anticipated development timelines, which are subject to risks and uncertainties. We may, in some cases, use terms such as "predicts," "believes," "potential," "proposed," "continue," "estimates," "anticipates," "expects," "plans," "intends," "may," "could," "might," "will," "should," or other words that convey uncertainty of future events or outcomes to identify these forward-looking statements. Such statements are subject to numerous important factors, risks, and uncertainties that may cause actual events or results to differ materially from our current expectations, including, but not limited to, the risks that preliminary, interim and top-line clinical trial results may not be indicative of, and may differ from, final clinical data; that unfavorable new clinical trial data may emerge in ongoing clinical trials or through further analyses of existing clinical trial data; that earlier non-clinical and clinical data and testing of may not be predictive of the results or success of later clinical trials; and that that clinical trial data are subject to differing interpretations and assessments, including by regulatory authorities. These and other risks and uncertainties are more fully described in our periodic filings with the Securities and Exchange Commission (SEC), including the risk factors described in the section entitled "Risk Factors" in the quarterly and annual reports that we file with the SEC. Any forward-looking statements that we make in this press release speak only as of the date of this press release. Except as required by law, we assume no obligation to update forward-looking statements contained in this press release whether as a result of new information, future events, or otherwise, after the date of this press release.

关于前瞻性陈述的警示说明
本新闻稿包含1995年《私人证券诉讼改革法》所指的前瞻性陈述, 包括但不限于关于现有数据的定性评估、潜在益处、对正在进行的临床试验的预期、预期的监管申报和预期的开发时间表的声明, 它们受到风险和不确定性的影响。在某些情况下,我们可能会使用 “预测”、“相信”、“潜在”、“提议”、“继续”、“估计”、“预期”、“预期”、“计划”、“打算”、“可能”、“可能”、“可能”、“将”、“应该” 等术语或其他表达未来事件或结果不确定性的词语来识别这些前瞻性陈述。此类陈述受许多重要因素、风险和不确定性的影响,这些因素、风险和不确定性可能导致实际事件或结果与我们当前的预期存在重大差异,i包括但不限于以下风险:初步、中期和一线临床试验结果可能不代表最终临床数据,也可能与最终临床数据有所不同;正在进行的临床试验或通过对现有临床试验数据的进一步分析可能会出现不利的新临床试验数据;早期的非临床和临床数据及测试可能无法预测后期临床试验的结果或成功;以及临床试验数据受不同的解释和评估,包括监管机构的评估。我们在向美国证券交易委员会(SEC)提交的定期文件中更全面地描述了这些风险和不确定性,包括我们向美国证券交易委员会(SEC)提交的季度和年度报告中题为 “风险因素” 的部分中描述的风险因素。我们在本新闻稿中所作的任何前瞻性陈述仅代表截至本新闻稿发布之日。除非法律要求,否则在本新闻稿发布之日之后,无论是由于新信息、未来事件还是其他原因,我们都没有义务更新本新闻稿中包含的前瞻性陈述。

Contact:
Tiffany Hamilton
Head of Communications
Tiffany.Hamilton@ocugen.com

联系人:
蒂芙尼汉密尔顿
传播主管
Tiffany.Hamilton@ocugen.com

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