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Cedar Clinical Research Selected as Clinical Research Site for Cybin's Phase 3 Study of CYB003

Cedar Clinical Research Selected as Clinical Research Site for Cybin's Phase 3 Study of CYB003

Cedar 臨床研究被選爲 Cybin 的 CYB003 三期研究的臨床研究地點
PR Newswire ·  04/17 19:00

VANCOUVER, BC, April 17, 2024 /PRNewswire/ - Numinus Wellness Inc. ("Numinus" or the "Company") (TSX: NUMI) (OTCQX: NUMIF), a mental health care company advancing traditional and innovative behavioral health treatments with a focus on safe, evidence-based novel therapies, is proud to announce that its research site, Cedar Clinical Research ("CCR"), has been chosen as one of multiple sites for Cybin's Phase 3 pivotal, multinational clinical trial of CYB003 for the adjunctive treatment of Major Depressive Disorder ("MDD").

不列顛哥倫比亞省溫哥華,2024 年 4 月 17 日 /PRNewswire/-Numinus Wellness Inc. (”Numinus“或者”公司“)(多倫多證券交易所股票代碼:NUMI)(OTCQX:NUMIF)是一家推進傳統和創新行爲健康治療的心理保健公司,專注於安全、循證的新療法。該公司自豪地宣佈,其研究機構Cedar Clinical Research(“CCR”)已被選爲Cybin用於輔助治療重度抑鬱症的 CYB003 三期關鍵跨國臨床試驗的多個研究中心之一(“” MDD”)。

In its recently completed Phase 2 trial in participants with moderate to severe major depressive disorder, Cybin reported that at four months after dosing, 75% of patients receiving two 16mg doses of CYB003 achieved remission from depression symptoms. With the Phase 2 trial data, the U.S. Food and Drug Administration ("FDA") granted CYB003 breakthrough therapy designation, potentially shortening the drug development timeline.

在最近完成的針對中度至重度重度抑鬱症參與者的2期試驗中,Cybin報告說,在給藥四個月後,接受兩劑16mg劑量CYB003 的患者中有75%緩解了抑鬱症狀。根據二期試驗數據,美國食品藥品監督管理局(“FDA”)授予了 CYB003 突破性療法稱號,這有可能縮短藥物研發時間。

The Phase 3 trial for CYB003 is planned to commence enrollment mid-2024 and focus on its safety and efficacy. CCR's Murray, Utah, location will be one of the 15 U.S. sites. Dr. Paul Thielking, Chief Science Officer of Numinus, will be the Principal Investigator.

CYB003 的 3 期試驗計劃於 2024 年中期開始入組,重點關注其安全性和有效性。CCR位於猶他州默裏的地點將成爲美國15個基地之一。Numinus首席科學官保羅·蒂爾金博士將擔任首席研究員。

"The Phase 2 results from the CYB003 trials were impressive and demonstrated the potential for treating a serious condition that affects over 20 million Americans," said Dr. Thielking. "We look forward to working with Cybin on the Phase 3 trials to add to the knowledge of CYB003's efficacy and address an important unmet need in patient care."

蒂爾金博士說:“CYB003 試驗的第二階段結果令人印象深刻,表明有可能治療一種影響2000多萬美國人的嚴重疾病。”“我們期待與Cybin合作進行3期試驗,以增加對 CYB003 療效的了解,並解決患者護理中尚未滿足的重要需求。”

"With many drug candidates advancing to later stages of clinical trials, 2024 is turning out to be a critical year for psychedelic-assisted therapy," added Payton Nyquvest, Numinus Founder and CEO. "We are proud of our role in working with drug developers to facilitate the important research that will help move these candidates to FDA approval and, ultimately, patient care."

Numinus創始人兼首席執行官Payton Nyquvest補充說:“隨着許多候選藥物進入臨床試驗的後期階段,2024年是迷幻輔助療法的關鍵一年。”“我們爲我們在與藥物開發商合作促進重要研究方面所發揮的作用感到自豪,這將有助於這些候選藥物獲得美國食品藥品管理局的批准,並最終促進患者護理。”

To learn more about enrolling in the CYB003 Phase 3 Trial, please visit this link.

要了解有關報名參加 CYB003 第 3 階段試驗的更多信息,請訪問此鏈接。

About Numinus
關於 Numinus

Numinus Wellness Inc. (TSX: NUMI) helps people to heal and be well through the development and delivery of innovative mental health care and access to safe, evidence-based psychedelic-assisted therapies. The Numinus model – including psychedelic research and clinic care – is at the forefront of a transformation aimed at healing rather than managing symptoms for depression, anxiety, trauma, pain and substance use. At Numinus, we are leading the integration of psychedelic-assisted therapies into mainstream clinical practice and building the foundation for a healthier society.

Numinus Wellness Inc.(多倫多證券交易所股票代碼:NUMI)通過開發和提供創新的心理保健以及獲得安全、循證的迷幻輔助療法,幫助人們康復和健康。包括迷幻研究和臨床護理在內的Numinus模型處於轉型的最前沿,該轉型旨在治癒而不是控制抑鬱、焦慮、創傷、疼痛和藥物濫用症狀。在Numinus,我們正在領導將迷幻輔助療法納入主流臨床實踐,併爲更健康的社會奠定基礎。

Learn more at and follow us on LinkedIn, Facebook, and Instagram.

要了解更多信息,請訪問 然後關注我們 領英Facebook,以及 Instagram

Forward-looking statements
前瞻性陳述

Statements and other information contained in this press release about anticipated future events constitute forward-looking statements. Forward-looking statements are often, but not always, identified by the use of words such as "seek", "anticipate", "believe", "plan", "estimate", "expect" and "intend" and statements that an event "may", "will", "should", "could" or "might" occur or other similar expressions. Forward-looking statements are subject to risks and uncertainties and other factors that could cause actual results to differ materially from those contained in the forward-looking statements, including challenges and uncertainties inherent in product and/or treatment development and in the psychedelics industry generally, availably of suitable subjects, the uncertainties of clinical success, the possibility of adverse events, and the timeline for the availability of the treatment under investigation; the laws, challenges and risks involved in the production of a psychedelics drug; and the uncertainty of the level of demand, uptake and/or insurance coverage for treatment other risks that are set forth in and other risks that are set forth in our annual information form dated November 29, 2023 and available on SEDAR at . Forward-looking statements are based on estimates and opinions of management at the date the statements are made. Numinus does not undertake any obligation to update forward-looking statements even if circumstances or management's estimates or opinions should change except as required by applicable laws. Investors should not place undue reliance on forward-looking statements.

本新聞稿中包含的有關未來預期事件的陳述和其他信息構成前瞻性陳述。前瞻性陳述通常使用 “尋找”、“預測”、“相信”、“計劃”、“估計”、“期望” 和 “打算” 等詞語以及關於某一事件 “可能”、“將”、“應該”、“可能” 或 “可能” 發生的陳述或其他類似的表述來識別。前瞻性陳述受風險和不確定性以及其他因素的影響,這些因素可能導致實際結果與前瞻性陳述中包含的結果存在重大差異,包括產品和/或治療開發以及迷幻藥行業普遍存在的挑戰和不確定性、合適受試者的可用性、臨床成功的不確定性、不良事件的可能性以及所研究治療的上市時間表;生產所涉及的法律、挑戰和風險迷幻藥物;以及治療需求、吸收和/或保險承保水平的不確定性、列出的其他風險和其他風險,這些風險載於我們2023年11月29日的年度信息表中,可在SEDAR上查閱 。前瞻性陳述基於陳述發表之日管理層的估計和意見。除非適用法律要求,否則即使情況或管理層的估計或意見發生變化,Numinus也沒有義務更新前瞻性陳述。投資者不應過分依賴前瞻性陳述。

SOURCE Numinus Wellness Inc.

來源 Numinus 健康公司

譯文內容由第三人軟體翻譯。


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