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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 年会上公布了首批临床前数据,重点介绍了 IL-10 INDUKINE 分子作为炎症性肠病 (IBD) 的潜在疗法
GlobeNewswire ·  04/23 08:00

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

首批数据表明PREDATOR平台在免疫介导疾病中的应用

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.

马萨诸塞州沃特敦,2024年4月23日(GLOBE NEWSWIRE)——Werewolf Therapeutics, Inc.(“公司” 或 “狼人”)(纳斯达克股票代码:HOWL)今天在免疫学发布了一张海报,展示了动物模型中用于治疗结肠炎的条件激活 IL-10 INDUKINE 分子的特征数据,这是一种利用其 PREDATOR 蛋白工程平台的新方法TM 2024年,美国免疫学家协会(AAI)年会将于5月3日至7日在伊利诺伊州芝加哥举行。

"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总裁兼首席执行官丹尼尔·希克林博士表示:“随着我们将平台的应用从癌症扩展到免疫学和炎症(I&I)领域,Werewolf很高兴分享这些初步数据,以支持我们独特的条件活性细胞因子免疫疗法用于IBD的潜在治疗。”“尽管IBD的治疗取得了进展,但某些患者亚群要么对现有疗法没有反应,要么失去了反应,这突显了对更多治疗选择的明显需求。”

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.

根据美国疾病控制与预防中心的数据,IBD这个术语包括两种疾病,即克罗恩氏病和溃疡性结肠炎(UC),其特征是胃肠道(GI)的慢性炎症。长期的炎症会导致胃肠道受损。尽管IBD的确切原因尚不清楚,但已证明自身免疫和免疫介导因素会导致该疾病的严重程度。克罗恩病和结肠炎基金会领导的一项开创性研究发现,超过0.7%的美国人诊断出IBD,每10万人中有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).

一张名为 “条件活性 IL-10 INDUKINE 的开发” 的海报总结了突出狼人发现的结果TM 用于治疗炎症性肠病的分子”(委员会 #B906)。

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

关键要点是狼人的 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.
  • 包含人类 IL-10、阻断结构域和半衰期扩展结构域,该结构域由专有的蛋白酶敏感链接物连接在一起,这些链接剂由 UC 和 Crohn 的人体结肠样本分解;
  • 在发炎的结肠中处于外周无活性和条件性活跃状态,由于蛋白酶失调环境中连接物的裂解,IL-10 会在结肠局部释放;以及
  • 在小鼠结肠炎模型中,防止体重减轻和肠道组织学损伤,抑制结肠内炎症细胞因子的产生。

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

该海报可于 2024 年 5 月 6 日星期一在 B906 号船上亲自观看,狼人代表将于下午 2:15-3:30 到场回答问题。该海报也将在我们的网站上公布,网址为

About Werewolf Therapeutics

关于狼人疗法

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. 是一家创新的生物制药公司,率先开发旨在刺激人体免疫系统的疗法,用于治疗癌症和其他免疫介导疾病。我们正在利用我们专有的PREDATOR平台来设计刺激适应性和先天免疫的条件激活分子,目标是解决传统促炎免疫疗法的局限性。我们的INDUKINE分子旨在在外周组织中保持非活性,但在肿瘤微环境中有选择地激活。我们最先进的临床阶段候选产品 WTX-124 和 WTX-330 分别是系统输送、条件激活的白介素-2(IL-2)和白介素-12(IL-12)INDUKINE分子,用于治疗实体瘤。我们预计将作为单一药物推进多种肿瘤类型的 WTX-124,与免疫检查点抑制剂联合使用,在多种肿瘤类型中推进 WTX-330 或作为单一药物治疗非霍奇金淋巴瘤。要了解更多信息,请访问 。

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.

关于前瞻性陈述的警示说明
本新闻稿包含涉及重大风险和不确定性的前瞻性陈述。根据1995年《私人证券诉讼改革法》,本新闻稿中包含的所有陈述,包括有关狼人未来运营、前景、计划以及候选产品在临床前和临床研究中的潜在活动和功效的陈述,均构成前瞻性陈述。“目标”、“预测”、“相信”、“考虑”、“继续”、“可以”、“设计”、“估计”、“期望”、“目标”、“打算”、“可能”、“目标”、“目标”、“持续”、“计划”、“潜力”、“预测”、“项目”、“承诺”、“应该”、“目标”、“目标”、“持续”、“计划”、“潜力”、“预测”、“项目”、“承诺”、“应该”、“目标”、“目标”、“正在进行中”、“计划”、“潜力”、“预测”、“项目”、“承诺”、“应该”、“目标”、“目标”、“正在进行中”、“计划”” “将” 或 “将”,或这些术语的否定词或其他类似术语旨在识别前瞻性陈述,尽管并非所有前瞻性陈述都包含这些识别词。公司可能无法实际实现这些前瞻性陈述中披露的计划、意图或预期,您不应过分依赖这些前瞻性陈述。由于各种重要因素,实际结果或事件可能与这些前瞻性陈述中披露的计划、意图和预期存在重大差异,包括:候选产品开发固有的不确定性,包括研究活动的开展、临床前研究和临床试验的启动和完成;临床前研究结果的可用性和时间的不确定性;临床前研究的结果是否可以预测以后的临床前研究结果;以及临床试验;以及公司于2024年3月7日向美国证券交易委员会(“SEC”)提交的10-K表格的 “风险因素” 部分以及公司随后可能向美国证券交易委员会提交的文件中确定的风险和不确定性。此外,本新闻稿中包含的前瞻性陈述代表了公司截至本演讲之日的观点。该公司预计,随后的事件和事态发展将导致其观点发生变化。但是,尽管公司可能会选择在未来的某个时候更新这些前瞻性陈述,但它明确表示不承担任何更新这些前瞻性陈述的义务。不应将这些前瞻性陈述视为本新闻稿发布之日后任何日期的公司观点。

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

投资者联系人:
乔什·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

媒体联系人:
阿曼达塞尔斯
VERGE 科学通讯
301.332.5574
asellers@vergescientific.com

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

公司联系人:
艾伦·卢布曼
首席商务官
狼人疗法
elubman@werewolftx.com


声明:本内容仅用作提供资讯及教育之目的,不构成对任何特定投资或投资策略的推荐或认可。 更多信息
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