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Annovis Announces Unblinding of the Buntanetap Phase III Data in Parkinson's Disease

Annovis Announces Unblinding of the Buntanetap Phase III Data in Parkinson's Disease

Annovis宣佈對帕金森氏病的Buntanetap III期數據進行解盲
Annovis Bio ·  05/09 00:00

Thu, 09 May 2024

2024 年 5 月 9 日星期四

MALVERN, Pa., May 09, 2024 (GLOBE NEWSWIRE) -- Annovis Bio, Inc. (NYSE: ANVS) ("Annovis" or the "Company"), a clinical-stage drug platform company developing novel therapies for neurodegenerative diseases, today announced successful completion of data cleaning for its Phase III study of buntanetap in patients with early Parkinson's disease (PD). Topline efficacy data is expected in June.

賓夕法尼亞州馬爾文,2024年5月9日(GLOBE NEWSWIRE)——開發神經退行性疾病新療法的臨床階段藥物平台公司Annovis Bio, Inc.(紐約證券交易所代碼:ANVS)(“Annovis” 或 “公司”)今天宣佈,成功完成了對早期帕金森氏病(PD)患者buntanetap的III期研究的數據清理。主要療效數據預計將於6月公佈。

The Phase III study was completed in 4Q 2023 with an original plan for data announcement in 1Q 2024, however the Company faced a delay in the process of data cleaning beyond the original prognosis. Maria Maccecchini, Ph.D., Founder, President, and CEO of Annovis, explains in detail the reason behind this delay:

第三階段研究於2023年第四季度完成,最初計劃在2024年第一季度公佈數據,但是該公司在數據清理過程中面臨延遲,超出了最初的預期。Annovis創始人、總裁兼首席執行官瑪麗亞·馬切基尼博士詳細解釋了延遲的原因:

"When we reached the point of unblinding the data for the PD Phase III study, we discovered an unexpected issue: too many plasma samples showed no presence of buntanetap. We were expecting 33% blank samples from the placebo group, but we saw over 50% blank samples. We were afraid that we had mixed up bottles and that patients weren't given what they were supposed to. If that had happened, the study would have been worthless. We promptly started searching for a possible explanation at every step of the way. We checked the content of the bottles – correct. We checked the distribution of the bottles – correct. We checked the labeling of the plasma samples – correct. We checked the distribution of the plasma samples – correct. So, we were left with the pharmacokinetic (PK) measurements. PK is measured by LC-MS/MS with a very expensive set of equipment under GLP, GCP, GMP, and is regulated by very strict FDA rules. It turns out that the group, which was evaluating the PK, modified the method, unfortunately affecting the measurements. We repeated the PK of the same samples and obtained an expected 33% of blank samples accounting for placebo.

“當我們達到解密PD III期研究數據的地步時,我們發現了一個意想不到的問題:太多的血漿樣本顯示不存在buntanetap。我們原本預計安慰劑組中有33%的空白樣本,但我們看到的空白樣本超過50%。我們擔心自己把瓶子弄混了,而且病人得不到他們應該得到的東西。如果發生這種情況,這項研究將毫無價值。我們立即開始在每一步尋找可能的解釋。我們檢查了瓶子裏的東西,沒錯。我們檢查了瓶子的分佈情況——正確。我們檢查了血漿樣本的標籤——正確。我們檢查了血漿樣本的分佈——正確。因此,我們只剩下藥代動力學(PK)測量結果。PK 由 LC-MS/MS 測量,使用一套非常昂貴的設備,符合 GLP、GCP、GMP,並受非常嚴格的美國食品和藥物管理局法規的監管。事實證明,正在評估PK的該小組修改了方法,不幸的是影響了測量。我們重複了相同樣本的PK,預計佔安慰劑的空白樣本的33%。

The whole process took us 2 months, which caused the delay in data announcement. However, due to our effort and immediate actions, we are now confident and ready to evaluate the data for the public and the FDA and report topline results in June.

整個過程花了我們兩個月,這導致了數據公佈的延遲。但是,由於我們的努力和立即採取的行動,我們現在有信心並準備爲公衆和美國食品藥品管理局評估數據,並在6月報告主要結果。

Thank you very much for your understanding and patience."

非常感謝你的理解和耐心。”

About Annovis Bio, Inc.

關於 Annovis Bio, Inc.

Headquartered in Malvern, Pennsylvania, Annovis Bio, Inc. is a clinical-stage, drug platform company addressing neurodegeneration, such as Alzheimer's Disease (AD), Parkinson's Disease (PD), and other chronic neurodegenerative diseases. It is believed to be the only company developing a drug for both AD and PD designed to inhibit more than one neurotoxic protein to restore axonal and synaptic activity. By improving brain function, the company's goal is to treat memory loss and dementia associated with AD as well as body and brain dysfunction associated with PD. For more information on Annovis Bio, please visit the Company's website www.annovisbio.com and follow us on LinkedIn and X (formerly known as Twitter).

Annovis Bio, Inc. 總部位於賓夕法尼亞州馬爾文,是一家臨床階段的藥物平台公司,致力於治療神經變性,例如阿爾茨海默氏病(AD)、帕金森氏病(PD)和其他慢性神經退行性疾病。據信它是唯一一家同時開發AD和PD藥物的公司,該藥物旨在抑制一種以上的神經毒性蛋白質,以恢復軸突和突觸活性。通過改善大腦功能,該公司的目標是治療與AD相關的記憶力減退和癡呆以及與PD相關的身體和大腦功能障礙。有關Annovis Bio的更多信息,請訪問該公司的網站 www.annovisbio.co 然後關注我們 領英X(原名推特)

Forward-Looking Statements

前瞻性陳述

This press release contains "forward-looking" statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. All statements other than statements of historical fact are statements that could be deemed forward-looking statements. The Company advises caution in reliance on forward-looking statements. Forward-looking statements include, without limitation, the Company's plans related to clinical trials. These statements involve known and unknown risks, uncertainties and other factors that may cause actual results to differ materially from those implied by forward-looking statements, including regarding patient enrollment, the effectiveness of Buntanetap and the timing, effectiveness, and anticipated results of the Company's clinical trials evaluating the efficacy, safety and tolerability of buntanetap. See also additional risk factors set forth in the Company's periodic filings with the SEC, including, but not limited to, those risks and uncertainties listed in the section entitled "Risk Factors," in the Company's Annual Report on Form 10-K and Quarterly Reports on Form 10-Q filed with the SEC. All forward-looking statements in this press release are based on information available to the Company as of the date of this filing. The Company expressly disclaims any obligation to update or alter its forward-looking statements, whether as a result of new information, future events or otherwise, except as required by applicable law.

本新聞稿包含經修訂的1933年《證券法》第27A條和經修訂的1934年《證券交易法》第21E條所指的 “前瞻性” 陳述。除歷史事實陳述以外的所有陳述均可被視爲前瞻性陳述。該公司建議謹慎對待前瞻性陳述。前瞻性陳述包括但不限於公司與臨床試驗相關的計劃。這些陳述涉及已知和未知的風險、不確定性和其他因素,這些因素可能導致實際結果與前瞻性陳述所暗示的結果存在重大差異,包括患者入組、Buntanetap的有效性以及公司評估buntanetap療效、安全性和耐受性的臨床試驗的時機、有效性和預期結果。另請參閱公司向美國證券交易委員會提交的定期文件中列出的其他風險因素,包括但不限於公司向美國證券交易委員會提交的10-K表年度報告和10-Q表季度報告中 “風險因素” 部分中列出的風險和不確定性。本新聞稿中的所有前瞻性陳述均基於公司截至本申報之日獲得的信息。除非適用法律要求,否則公司明確表示不承擔任何更新或修改其前瞻性陳述的義務,無論是由於新信息、未來事件還是其他原因。

Investor Contact:

投資者聯繫人:

Maria Maccecchini, Ph.D.

瑪麗亞·馬切基尼博士

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Source: Annovis Bio Inc.

資料來源:Annovis Bio Inc.

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