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Ocugen Announces OCU400—Modifier Gene Therapy—Phase 1/2 Data Presentation At Retinal Cell and Gene Therapy Innovation Summit 2024

Ocugen Announces OCU400—Modifier Gene Therapy—Phase 1/2 Data Presentation At Retinal Cell and Gene Therapy Innovation Summit 2024

Ocugen宣布在2024年视网膜细胞和基因疗法创新峰会上发布OCU400——修改基因疗法——1/2期数据
Ocugen ·  04/29 00:00

MALVERN, Pa., April 29, 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 Benjamin Bakall, MD, PhD, Director of Clinical Research at Associated Retina Consultants and Clinical Assistant Professor at the University of Arizona, College of Medicine—Phoenix will present data from the OCU400 Phase 1/2 clinical trial at the Retinal Cell and Gene Therapy Innovation Summit being held May 3, 2024 in Seattle, WA.

宾夕法尼亚州马尔文,2024年4月29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, Inc.(OCUGEN或公司)(纳斯达克股票代码:OCGN)今天宣布,医学博士、Associated Retina Consultants临床研究主任、亚利桑那大学医学院临床助理教授本杰明·巴卡尔医学博士 —菲尼克斯将在2024年5月3日举行的视网膜细胞和基因疗法创新峰会上公布 OCU400 1/2 期临床试验的数据华盛顿州西雅图。

"I look forward to sharing more about my clinical experience with this novel modifier gene therapy with my peers and industry leadership during the summit," said Dr. Bakall. "There remains a significant unmet need for patients with retinitis pigmentosa (RP) and I believe that this approach can offer a new therapeutic option to address the disease itself."

巴卡尔博士说:“我期待在峰会期间与同行和行业领导者更多地分享我使用这种新型修饰基因疗法的临床经验。”“色素性视网膜炎(RP)患者的大量需求仍未得到满足,我相信这种方法可以为治疗该疾病本身提供新的治疗选择。”

The Retinal Cell and Gene Therapy Innovation Summit 2024 is jointly organized by the Foundation Fighting Blindness and the Oregon Health and Science University Casey Eye Institute. The Summit brings together representatives from the biotech and pharma industries, along with members of the medical and research communities, to discuss rapidly emerging ocular gene and cell therapies and strategize how to move the most advanced retinal disease therapies toward clinical utility.

2024年视网膜细胞和基因疗法创新峰会由抗击失明基金会和俄勒冈健康与科学大学凯西眼科研究所联合举办。峰会汇集了来自生物技术和制药行业的代表以及医学和研究界的成员,讨论快速崛起的眼部基因和细胞疗法,并制定如何将最先进的视网膜疾病疗法转向临床应用的战略。

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

巴卡尔博士的演讲详情如下:

Presentation Title: "Nuclear Hormone Receptor-Based Gene Modifier Therapy: Safety and Efficacy from Phase 1/2 Clinical Trials for Retinitis Pigmentosa"
Date: Friday, May 3, 2024
Time: 10:50 – 11:05 a.m. (PT)
Location: Hyatt Regency Seattle

演讲题目:“基于核激素受体的基因修饰疗法:色素性视网膜炎1/2期临床试验的安全性和有效性”
日期:2024 年 5 月 3 日星期五
时间:上午 10:50 — 11:05(太平洋时间)
地点:西雅图凯悦酒店

The OCU400 Phase 3 liMeliGhT clinical trial is currently underway and on track to meet the Company's 2026 BLA and MAA approval targets. Between the U.S. and EU, nearly 300,000 people are affected by RP.

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。在美国和欧盟之间,有近30万人受到RP的影响。

About OCU400
OCU400 is the Company's gene-agnostic modifier gene therapy product based on 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.

关于 OCU400
OCU400 是该公司基于 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。

About RP
RP is a group of rare, genetic disorders that involve a breakdown and loss of cells in the retina, leading to vision loss and blindness. Currently, RP is associated with mutations in more than 100 genes. There are no approved treatment options that slow or stop the progression of multiple forms of RP. Proposed treatments for RP include gene replacement therapy, retinal implant devices, retinal transplantation, stem cells, vitamin therapy, and other pharmacological treatments. Current gene replacement therapies are promising but are limited to treating just a single mutation. In addition, while gene therapies may provide a new functional gene, they do not necessarily eliminate the underlying genetic defect, which may still cause stress and toxic effects leading to retina degeneration. Therefore, the development of gene-specific replacement therapy is highly challenging, especially when multiple and unknown genes are involved. Thus, novel therapeutic approaches targeting broader RP disease in a gene-agnostic manner offer greater hope for patients.

关于 RP
RP 是一组罕见的遗传性疾病,涉及视网膜细胞的分解和流失,导致视力丧失和失明。目前,RP与100多个基因的突变有关。目前尚无经批准的减缓或阻止多种形式的 RP 进展的治疗方案。RP 的拟议治疗方法包括基因替代疗法、视网膜植入设备、视网膜移植、干细胞、维生素疗法和其他药物治疗。目前的基因替代疗法前景看好,但仅限于治疗单一突变。此外,尽管基因疗法可以提供新的功能基因,但它们不一定能消除潜在的遗传缺陷,这种缺陷仍可能导致压力和毒性作用,导致视网膜变性。因此,基因特异性替代疗法的开发极具挑战性,尤其是在涉及多个未知基因时。因此,以与基因无关的方式针对更广泛的RP疾病的新型治疗方法为患者提供了更大的希望。

About 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.

关于 Ocugen, Inc.
Ocugen, Inc. 是一家生物技术公司,专注于发现、开发和商业化新型基因和细胞疗法以及改善健康状况并为全球患者带来希望的疫苗。我们正在通过勇敢的创新对患者的生活产生影响——利用我们独特的智力和人力资本开辟新的科学道路。我们的突破性修饰基因疗法平台有可能使用单一产品治疗多种视网膜疾病,并且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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