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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 宣佈 CSO 將在 2024 年國際細胞與基因療法學會上發表關於改性基因療法的演講
Ocugen ·  05/20 12:00

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.

賓夕法尼亞州馬爾文,2024年5月20日(GLOBE NEWSWIRE)——專注於發現、開發和商業化新型基因和細胞療法及疫苗的生物技術公司Ocugen公司(Ocugen或公司)(納斯達克股票代碼:OCGN)今天宣佈,奧庫根首席科學官兼研發主管阿倫·烏帕迪亞博士將在國際細胞與基因療法學會發表演講 (ISCT) 年會將於 2024 年 5 月 29 日至 6 月 1 日在加拿大溫哥華舉行。

"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博士說:“我很高興向一個致力於將細胞和基因療法轉化爲安全有效的治療以改善患者生活的組織提供 OCU400 數據。”“OCU400 修飾基因療法是潛在治療更廣泛的色素性視網膜炎(RP)和萊伯先天性黑蒙症(LCA)疾病的突破性方法,這兩種疾病涉及 100 多個突變。”

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 提供尖端的翻譯內容,並有機會與來自學術機構、監管機構和醫療保健行業的全球專家建立聯繫。與會者可以參與激烈的辯論,合作開發應對行業挑戰的解決方案,並參與推進細胞和基因療法領域的對話。

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

Upadhyay博士的演講詳情如下:

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

最新口頭摘要會議:用於治療色素性視網膜炎的 OCU400 修飾基因療法的 1/2 期臨床試驗的安全性和有效性結果

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
時間:太平洋夏令時間下午 5 點至 6 點
地點:溫哥華會議中心西樓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博士的海報也將在太平洋夏令時間2024年5月29日星期三晚上7點至8點30分的海報社交會議 #1 期間公佈。

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 臨床試驗目前正在進行中,有望實現公司 2026 年 BLA 和 MAA 的批准目標。OCU400 是第一個進入第 3 階段且具有廣泛的 RP 適應症的基因治療計劃。

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.

關於 OCU400
OCU400 是該公司基於核激素受體 (NHR) 基因的基因無關修飾基因療法產品, NR2E3NR2E3 調節視網膜內的各種生理功能,例如感光器發育和維持、新陳代謝、光轉導、炎症和細胞存活網絡。通過其驅動功能,OCU400 重置改變/受影響的細胞基因網絡並建立動態平衡狀態,這種平衡狀態有可能改善 RP 患者的視網膜健康和功能。在美國和歐盟,總共有近30萬人受到RP的影響。

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.

關於修飾基因療法
修飾基因療法旨在滿足與視網膜疾病相關的未滿足的醫療需求,包括IRD,例如RP、LCA和Stargardt病,以及乾性年齡相關性黃斑變性(dAMD)等多因素疾病。我們的修飾基因療法平台基於主基因調節劑NHR的使用,它有可能恢復動態平衡——視網膜中的基本生物學過程。與僅針對一種基因突變的單基因替代療法不同,我們認爲,我們的修飾基因療法平台通過使用NHR,代表了一種新方法,有可能使用一種產品解決由多個基因突變引起的多種視網膜疾病,並解決可能由多個基因網絡失衡引起的複雜疾病。目前,Ocugen在臨床上有三個修飾基因療法項目:OCU400、OCU410 和 OCU410ST。除了 OCU400 三期 LimeLight 臨床試驗外,針對繼發於 dAMD 的地理萎縮 (GA) 的 OCU410 1/2 期 Armada 臨床試驗和針對 Stargardt 病的 OCU410ST 1/2 期 Gardian 臨床試驗目前正在進行中。在美國和歐盟,GA共影響約200萬至300萬人,Stargardt病共影響美國和歐盟的近10萬人。

About Ocugen, Inc.

關於 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. 是一家生物技術公司,專注於發現、開發和商業化能夠改善健康併爲全球患者帶來希望的新型基因和細胞療法和疫苗。我們正在通過勇敢的創新對患者的生活產生影響——開闢新的科學道路,利用我們獨特的智力和人力資本。我們的突破性修飾基因療法平台有可能用單一產品治療多種視網膜疾病,我們正在推進傳染病研究,以支持公共衛生和骨科疾病,以滿足未得到滿足的醫療需求。在以下網址了解更多 www.ocugen.com 然後關注我們 X領英

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.

關於前瞻性陳述的警示說明
本新聞稿包含1995年《私人證券訴訟改革法》所指的前瞻性陳述, 包括但不限於關於現有數據的定性評估、潛在益處、對正在進行的臨床試驗的預期、預期的監管申報和預期的開發時間表的聲明, 它們受到風險和不確定性的影響。在某些情況下,我們可能會使用 “預測”、“相信”、“潛在”、“提議”、“繼續”、“估計”、“預期”、“預期”、“計劃”、“打算”、“可能”、“可能”、“可能”、“將”、“應該” 等術語或其他表達未來事件或結果不確定性的詞語來識別這些前瞻性陳述。此類陳述受許多重要因素、風險和不確定性的影響,這些因素、風險和不確定性可能導致實際事件或結果與我們當前的預期存在重大差異,i包括但不限於以下風險:初步、中期和一線臨床試驗結果可能不代表最終臨床數據,也可能與最終臨床數據有所不同;正在進行的臨床試驗或通過對現有臨床試驗數據的進一步分析可能會出現不利的新臨床試驗數據;早期的非臨床和臨床數據及測試可能無法預測後期臨床試驗的結果或成功;以及臨床試驗數據受不同的解釋和評估,包括監管機構的評估。我們在向美國證券交易委員會(SEC)提交的定期文件中更全面地描述了這些風險和不確定性,包括我們向美國證券交易委員會(SEC)提交的季度和年度報告中題爲 “風險因素” 的部分中描述的風險因素。我們在本新聞稿中所作的任何前瞻性陳述僅代表截至本新聞稿發佈之日。除非法律要求,否則在本新聞稿發佈之日之後,無論是由於新信息、未來事件還是其他原因,我們都沒有義務更新本新聞稿中包含的前瞻性陳述。

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

聯繫人:
蒂芙尼漢密爾頓
傳播主管
Tiffany.Hamilton@ocugen.com

譯文內容由第三人軟體翻譯。


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