share_log

Werewolf Therapeutics Presents First Preclinical Data Highlighting IL-10 INDUKINE Molecules as a Potential Therapy for Inflammatory Bowel Disease (IBD) at AAI Annual Meeting

Werewolf Therapeutics Presents First Preclinical Data Highlighting IL-10 INDUKINE Molecules as a Potential Therapy for Inflammatory Bowel Disease (IBD) at AAI Annual Meeting

Werewolf Therapeutics 在 AAI 年會上公佈了首批臨床前數據,重點介紹了 IL-10 INDUKINE 分子作爲炎症性腸病 (IBD) 的潛在療法
GlobeNewswire ·  04/23 20:00

First Data Demonstrating Application of PREDATOR Platform in Immune-Mediated Diseases

首批數據表明PREDATOR平台在免疫介導疾病中的應用

WATERTOWN, Mass., April 23, 2024 (GLOBE NEWSWIRE) -- Werewolf Therapeutics, Inc. (the "Company" or "Werewolf") (Nasdaq: HOWL) today announced a poster presenting preclinical data characterizing conditionally-activated IL-10 INDUKINE molecules for the treatment of colitis in animal models, a novel approach leveraging its PREDATOR protein engineering platform, at IMMUNOLOGYTM 2024, the annual meeting of the American Association of Immunologists (AAI) taking place May 3-7 in Chicago, Illinois.

馬薩諸塞州沃特敦,2024年4月23日(GLOBE NEWSWIRE)——Werewolf Therapeutics, Inc.(“公司” 或 “狼人”)(納斯達克股票代碼:HOWL)今天在免疫學發佈了一張海報,展示了動物模型中用於治療結腸炎的條件激活 IL-10 INDUKINE 分子的特徵數據,這是一種利用其 PREDATOR 蛋白工程平台的新方法TM 2024年,美國免疫學家協會(AAI)年會將於5月3日至7日在伊利諾伊州芝加哥舉行。

"Werewolf is excited to share these preliminary data supporting our unique conditionally active cytokine immunotherapy approach for the potential treatment of IBD, as we extend applications of our platform from cancer to the immunology and inflammation (I&I) landscape," said Daniel J. Hicklin, Ph.D., President and Chief Executive Officer of Werewolf. "Despite progress in the treatment of IBD, certain patient subsets either fail to respond or lose responsiveness to existing therapies, underscoring a clear need for additional treatment options."

Werewolf總裁兼首席執行官丹尼爾·希克林博士表示:“隨着我們將平台的應用從癌症擴展到免疫學和炎症(I&I)領域,Werewolf很高興分享這些初步數據,以支持我們獨特的條件活性細胞因子免疫療法用於IBD的潛在治療。”“儘管IBD的治療取得了進展,但某些患者亞群要麼對現有療法沒有反應,要麼失去了反應,這突顯了對更多治療選擇的明顯需求。”

According to the Centers for Disease Control and Prevention, IBD is a term that encompasses two conditions, Crohn's disease and ulcerative colitis (UC), that are characterized by chronic inflammation of the gastrointestinal (GI) tract. Prolonged inflammation results in damage to the GI tract. While the exact cause of IBD is unknown, autoimmune and immune-mediated factors have been shown to contribute to the severity of the disease. A groundbreaking study led by the Crohn's & Colitis Foundation finds that IBD is diagnosed in more than 0.7% of Americans, with 721 cases per 100,000 people, or nearly 1 in 100.

根據美國疾病控制與預防中心的數據,IBD這個術語包括兩種疾病,即克羅恩氏病和潰瘍性結腸炎(UC),其特徵是胃腸道(GI)的慢性炎症。長期的炎症會導致胃腸道受損。儘管IBD的確切原因尚不清楚,但已證明自身免疫和免疫介導因素會導致該疾病的嚴重程度。克羅恩病和結腸炎基金會領導的一項開創性研究發現,超過0.7%的美國人診斷出IBD,每10萬人中有721例病例,接近每100人中有1例。

Results highlighting Werewolf's findings are summarized in a poster titled, "Development of Conditionally Active IL-10 INDUKINETM Molecules for the Treatment of Inflammatory Bowel Disease" (Board #B906).

一張名爲 “條件活性 IL-10 INDUKINE 的開發” 的海報總結了突出狼人發現的結果TM 用於治療炎症性腸病的分子”(委員會 #B906)。

Key takeaways are that Werewolf's IL-10 INDUKINE molecules:

關鍵要點是狼人的 IL-10 INDUKINE 分子:

  • Contain human IL-10, a blocking domain, and a half-life extension domain tethered together by proprietary protease-sensitive linkers that are cleaved by UC and Crohn's human colon samples;
  • Are peripherally inactive and conditionally active in the inflamed colon, where the IL-10 is released locally due to cleavage of the linkers in the dysregulated protease milieu; and
  • Prevent weight loss and intestinal histological damage and inhibit inflammatory cytokine production within the colon in mouse models of colitis.
  • 包含人類 IL-10、阻斷結構域和半衰期擴展結構域,該結構域由專有的蛋白酶敏感鏈接物連接在一起,這些鏈接劑由 UC 和 Crohn 的人體結腸樣本分解;
  • 在發炎的結腸中處於外周無活性和條件性活躍狀態,由於蛋白酶失調環境中連接物的裂解,IL-10 會在結腸局部釋放;以及
  • 在小鼠結腸炎模型中,防止體重減輕和腸道組織學損傷,抑制結腸內炎症細胞因子的產生。

The poster can be viewed in person on Monday, May 6, 2024, on board number B906, with Werewolf delegates present from 2:15-3:30pm to answer questions. The poster will also be available on our website at

該海報可於 2024 年 5 月 6 日星期一在 B906 號船上親自觀看,狼人代表將於下午 2:15-3:30 到場回答問題。該海報也將在我們的網站上公佈,網址爲

About Werewolf Therapeutics

關於狼人療法

Werewolf Therapeutics, Inc., is an innovative biopharmaceutical company pioneering the development of therapeutics engineered to stimulate the body's immune system for the treatment of cancer and other immune-mediated conditions. We are leveraging our proprietary PREDATOR platform to design conditionally activated molecules that stimulate both adaptive and innate immunity with the goal of addressing the limitations of conventional proinflammatory immune therapies. Our INDUKINE molecules are intended to remain inactive in peripheral tissue yet activate selectively in the tumor microenvironment. Our most advanced clinical stage product candidates, WTX-124 and WTX-330, are systemically delivered, conditionally activated Interleukin-2 (IL-2) and Interleukin-12 (IL-12) INDUKINE molecules, respectively, for the treatment of solid tumors. We expect to advance WTX-124 in multiple tumor types as a single agent and in combination with an immune checkpoint inhibitor and WTX-330 in multiple tumor types or Non-Hodgkin Lymphoma as a single agent. To learn more visit .

Werewolf Therapeutics, Inc. 是一家創新的生物製藥公司,率先開發旨在刺激人體免疫系統的療法,用於治療癌症和其他免疫介導疾病。我們正在利用我們專有的PREDATOR平台來設計刺激適應性和先天免疫的條件激活分子,目標是解決傳統促炎免疫療法的侷限性。我們的INDUKINE分子旨在在外周組織中保持非活性,但在腫瘤微環境中有選擇地激活。我們最先進的臨床階段候選產品 WTX-124 和 WTX-330 分別是系統輸送、條件激活的白介素-2(IL-2)和白介素-12(IL-12)INDUKINE分子,用於治療實體瘤。我們預計將作爲單一藥物推進多種腫瘤類型的 WTX-124,與免疫檢查點抑制劑聯合使用,在多種腫瘤類型中推進 WTX-330 或作爲單一藥物治療非霍奇金淋巴瘤。要了解更多信息,請訪問 。

Cautionary Note Regarding Forward-Looking Statements
This press release contains forward-looking statements that involve substantial risk and uncertainties. All statements, other than statements of historical facts, contained in this press release, including statements regarding Werewolf's future operations, prospects, plans, and the potential activity and efficacy of product candidates in preclinical and clinical studies constitute forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995. The words "aim," "anticipate," "believe," "contemplate," "continue," "could," "design," "designed to," "estimate," "expect," "goal," "intend," "may," "might," "objective," "ongoing," "plan," "potential," "predict," "project," "promise," "should," "target," "will," or "would," or the negative of these terms, or other comparable terminology are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. The Company may not actually achieve the plans, intentions or expectations disclosed in these forward-looking statements, and you should not place undue reliance on these forward-looking statements. Actual results or events could differ materially from the plans, intentions and expectations disclosed in these forward-looking statements as a result of various important factors, including: uncertainties inherent in the development of product candidates, including the conduct of research activities, the initiation and completion of preclinical studies and clinical trials; uncertainties as to the availability and timing of results from preclinical studies; whether results from preclinical studies will be predictive of the results of later preclinical studies and clinical trials; as well as the risks and uncertainties identified in the "Risk Factors" section of the Company's Form 10-K filed with the Securities and Exchange Commission ("SEC") on March 7, 2024, and in subsequent filings the Company may make with the SEC. In addition, the forward-looking statements included in this press release represent the Company's views as of the date of this presentation. The Company anticipates that subsequent events and developments will cause its views to change. However, while the Company may elect to update these forward-looking statements at some point in the future, it specifically disclaims any obligation to do so. These forward-looking statements should not be relied upon as representing the Company's views as of any date subsequent to the date of this press release.

關於前瞻性陳述的警示說明
本新聞稿包含涉及重大風險和不確定性的前瞻性陳述。根據1995年《私人證券訴訟改革法》,本新聞稿中包含的所有陳述,包括有關狼人未來運營、前景、計劃以及候選產品在臨床前和臨床研究中的潛在活動和功效的陳述,均構成前瞻性陳述。“目標”、“預測”、“相信”、“考慮”、“繼續”、“可以”、“設計”、“估計”、“期望”、“目標”、“打算”、“可能”、“目標”、“目標”、“持續”、“計劃”、“潛力”、“預測”、“項目”、“承諾”、“應該”、“目標”、“目標”、“持續”、“計劃”、“潛力”、“預測”、“項目”、“承諾”、“應該”、“目標”、“目標”、“正在進行中”、“計劃”、“潛力”、“預測”、“項目”、“承諾”、“應該”、“目標”、“目標”、“正在進行中”、“計劃”” “將” 或 “將”,或這些術語的否定詞或其他類似術語旨在識別前瞻性陳述,儘管並非所有前瞻性陳述都包含這些識別詞。公司可能無法實際實現這些前瞻性陳述中披露的計劃、意圖或預期,您不應過分依賴這些前瞻性陳述。由於各種重要因素,實際結果或事件可能與這些前瞻性陳述中披露的計劃、意圖和預期存在重大差異,包括:候選產品開發固有的不確定性,包括研究活動的開展、臨床前研究和臨床試驗的啓動和完成;臨床前研究結果的可用性和時間的不確定性;臨床前研究的結果是否可以預測以後的臨床前研究結果;以及臨床試驗;以及公司於2024年3月7日向美國證券交易委員會(“SEC”)提交的10-K表格的 “風險因素” 部分以及公司隨後可能向美國證券交易委員會提交的文件中確定的風險和不確定性。此外,本新聞稿中包含的前瞻性陳述代表了公司截至本演講之日的觀點。該公司預計,隨後的事件和事態發展將導致其觀點發生變化。但是,儘管公司可能會選擇在未來的某個時候更新這些前瞻性陳述,但它明確表示不承擔任何更新這些前瞻性陳述的義務。不應將這些前瞻性陳述視爲本新聞稿發佈之日後任何日期的公司觀點。

Investor Contact:
Josh Rappaport
Stern IR
212.362.1200
Josh.Rappaport@sternir.com

投資者聯繫人:
喬什·拉帕波特
Stern IR
212.362.1200
Josh.Rappaport@sternir.com

Media Contact:
Amanda Sellers
VERGE Scientific Communications
301.332.5574
asellers@vergescientific.com

媒體聯繫人:
阿曼達塞爾斯
VERGE 科學通訊
301.332.5574
asellers@vergescientific.com

Company Contact:
Ellen Lubman
Chief Business Officer
Werewolf Therapeutics
elubman@werewolftx.com

公司聯繫人:
艾倫·盧布曼
首席商務官
狼人療法
elubman@werewolftx.com


譯文內容由第三人軟體翻譯。


以上內容僅用作資訊或教育之目的,不構成與富途相關的任何投資建議。富途竭力但無法保證上述全部內容的真實性、準確性和原創性。
    搶先評論