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Ocugen to Present at BIO International Convention 2024

Ocugen to Present at BIO International Convention 2024

Ocugen 將出席 2024 年 BIO 國際大會
Ocugen ·  05/29 12:00

MALVERN, Pa., May 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 the Company will present at the 2024 BIO International Convention taking place in San Diego, CA from June 3 – 6, 2024.

賓夕法尼亞州馬爾文,2024年5月29日(環球新聞專線)——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,該公司將參加2024年6月3日至6日在加利福尼亞州聖地亞哥舉行的2024 BIO國際大會。

During the conference, Ocugen's leadership team will host meetings with potential partners and pharmaceutical executives to explore opportunities for the Company's dynamic pipeline addressing unmet medical needs—particularly its first-in-class ophthalmic modifier gene therapy and regenerative cell therapy platforms.

會議期間,Ocugen的領導團隊將與潛在的合作伙伴和製藥業高管舉行會議,探討公司的動態產品線解決未滿足的醫療需求的機會,尤其是其首創的眼科修飾基因療法和再生細胞療法平台。

"We are excited to return to BIO this year and showcase the significant advancements we've achieved both clinically and strategically," said Dr. Shankar Musunuri, Chairman, CEO, and Co-founder of Ocugen. "BIO is an important opportunity to pursue collaborations that will propel the development of our first-in-class therapies while also enhancing shareholder value. We eagerly anticipate engaging with the distinguished industry professionals in attendance."

Ocugen董事長、首席執行官兼聯合創始人尚卡爾·穆蘇努裏博士表示:“我們很高興今年能重返BIO,展示我們在臨床和戰略上取得的重大進展。”“BIO是開展合作的重要機會,這將推動我們首創療法的開發,同時提高股東價值。我們熱切期待與會的傑出行業專業人士互動。”

Ocugen's modifier gene therapy platform recently achieved several critical milestones, including the initiation of the OCU400 Phase 3 liMeLiGhT clinical trial for retinitis pigmentosa that affects approximately 300,000 people in the U.S. and Europe combined. Additionally, dosing was completed in Cohort 2 in both the OCU410 Phase 1/2 ArMaDa clinical trial for geographic atrophy secondary to dry age-related macular degeneration (2-3 million people in the U.S. and Europe combined) and OCU410ST Phase 1/2 GARDian trial for Stargardt disease (approximately 100,000 people in the U.S. and Europe combined).

Ocugen 的修飾基因療法平台最近取得了多個關鍵里程碑,包括啓動了針對色素性視網膜炎的 OCU400 三期 LimeLight 臨床試驗,該試驗共影響了美國和歐洲約30萬人。此外,針對繼發於乾性年齡相關性黃斑變性的地理萎縮的 OCU410 1/2 期 Armada 臨床試驗(美國和歐洲共有 2-3 萬人)和 OCU410ST 1/2 期 Gardian 試驗(美國和歐洲共有大約 10 萬人)中 2 隊列的給藥均已完成。

NeoCart is the Company's Phase 3-ready, pioneering regenerative cell therapy candidate utilizing an enhanced autologous cartilage repair approach. NeoCart has been shown to fully restore cartilage in as little as 6 months in some patients. NeoCart is the only autologous therapy utilizing a 3D scaffold and novel bioreactor to simulate compressive force and enhance cartilage cell differentiation. Recently, Ocugen completed its state-of the-art cell and gene therapy manufacturing facility.

NeoCart 是該公司採用增強型自體軟骨修復方法推出的三期就緒的開創性再生細胞療法候選藥物。事實證明,NeoCart可以在短短6個月內完全恢復某些患者的軟骨。NeoCart是唯一一種使用三維支架和新型生物反應器來模擬壓縮力和增強軟骨細胞分化的自體療法。最近,Ocugen完成了其最先進的細胞和基因療法制造工廠。

Ocugen's presentation details are as follows:

Ocugen的演示細節如下:

Event: BIO 2024 International Convention
Date: Monday, June 3, 2024
Time: 2:15 p.m. PT
Location: Presentation Theater 1 - Hall A - Exhibition Hall, San Diego Convention Center
Presenter: Dr. Shankar Musunuri, Chairman, CEO, and Co-founder

活動:BIO 2024 國際大會
日期:2024 年 6 月 3 日,星期一
時間:太平洋時間下午 2:15
地點:演示廳 1-A廳-展覽廳,聖地亞哥會議中心
主持人:Shankar Musunuri博士,董事長、首席執行官兼聯合創始人

Please visit Ocugen at Booth #3945 to learn more about the Company's clinical programs and the potential they may hold for patients.

請訪問Ocugen的 #3945 號展位,詳細了解該公司的臨床項目及其可能爲患者帶來的潛力。

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.

關於 Ocugen, Inc.
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,包括但不限於有關可用數據的定性評估、潛在收益、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,這些陳述受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,包括但不限於初步、中期和一線臨床試驗結果可能無法表示且可能與最終臨床數據不同的風險;在正在進行的臨床試驗中或通過對現有臨床試驗數據的進一步分析,可能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 of 可能無法預測後期臨床試驗的結果或成功與否;以及臨床試驗數據將受到不同的解釋和評估,包括監管機構的解釋和評估。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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