预约演示

更新于：2025-05-07

TMEM219

更新于：2025-05-07

基本信息

别名

IGFBP-3R、Insulin-like growth factor-binding protein 3 receptor、TMEM219

+ [1]

简介

Cell death receptor specific for IGFBP3, may mediate caspase-8-dependent apoptosis upon ligand binding.

关联

项与 TMEM219 相关的药物

Ebrasodebart

靶点

TMEM219

作用机制

TMEM219抑制剂

在研机构

Enthera Srl

原研机构

Enthera Srl

在研适应症

炎症性肠病 [+1]

非在研适应症-

最高研发阶段临床1期

首次获批国家/地区-

首次获批日期1800-01-20

项与 TMEM219 相关的临床试验

CTIS2023-507340-36-00

/ Not yet recruiting临床1期

- Ent001-CL-102

开始日期2024-04-22

申办/合作机构-

NL-OMON51546

/ RecruitingN/A

A phase 1, randomised, double-blind, placebo-controlled, single ascending dose study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics and immunogenicity of Ent001 in healthy subjects - Ent001 IV First in Human SAD Study in adult healthy subjects

开始日期2023-01-09

申办/合作机构-

100 项与 TMEM219 相关的临床结果

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100 项与 TMEM219 相关的转化医学

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0 项与 TMEM219 相关的专利（医药）

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项与 TMEM219 相关的文献（医药）

2025-06-01·European Journal of Medical Genetics

A rare triplication of 16p11.2: Unravelling the genomic complexity and review of the literature

Article

作者: van Haelst, Mieke M ; Haagmans, Martin A ; van der Smagt, Jasper J ; Henneman, Peter ; Roquas, Laura ; Kleinendorst, Lotte ; Koop, Klaas ; van der Laan, Liselot

16p11.2 triplication is a rare chromosomal disorder associated with developmental delay, behavioral abnormalities, and various dysmorphic features. Here, we present a case study of a four-year-old girl with 16p11.2 triplication, whose healthy father has a smaller 16p11.2 duplication that partially overlaps with that of the daughter. She has a global developmental delay, autism spectrum disorder, anxiety, and sensory processing issues, alongside dysmorphic features. Genetic analysis revealed triplication within the 16p11.2 duplication region. We used different technical approaches to pinpoint the exact genetic architecture of the triplication and to gain further functional insights. Using array-CGH and Fluorescence In Situ Hybridization (FISH), we detected the location of the triplication. We later sought to confirm this with Oxford Nanopore Technologies (ONT); however, detecting duplications and triplications proved to be challenging. Finally, RNA sequencing showed overexpression of genes within the triplication region, including INO80E, PAGR1, SPN, KIF22, HIRIP3, TAOK2, and TMEM219, some of which had been associated with neurodevelopmental disorders and/or increased body mass index by GWAS (1). Our findings contribute to the understanding of the phenotypic spectrum and molecular mechanisms of 16p11.2 triplication. Moreover, the challenges in detecting triplications using current sequencing methods highlight the need for improved diagnostic techniques.

2023-06-01·BioEssays : news and reviews in molecular, cellular and developmental biology

Targeting a novel apoptotic pathway in human disease.

Article

作者: Assi, Emma ; Petrazzuolo, Adriana ; Lunati, Maria Elena ; Fiorina, Paolo ; D'Addio, Francesca ; Bruckmann, Chiara ; Marin, Virna ; Pastore, Ida ; Montefusco, Laura

Apoptotic pathways have always been regarded as a key-player in preserving tissue and organ homeostasis. Excessive activation or resistance to activation of cell death signaling may indeed be responsible for several mechanisms of disease, including malignancy and chronic degenerative diseases. Therefore, targeting apoptotic factors gained more and more attention in the scientific community and novel strategies emerged aimed at selectively blocking or stimulating cell death signaling. This is also the case for the TMEM219 death receptor, which is activated by a circulating ligand, the Insulin-like growth factor binding protein 3 (IGFBP3) and induces a caspase-8-dependent apoptosis of the target cells. Interestingly, stimulation of the IGFBP3/TMEM219 axis exerts an anti-proliferative effect, while blockade of the TMEM219 deleterious signal protects TMEM219-expressing cells of the endocrine pancreas, lung, and intestine from damage and death. Here, we summarize the most updated reports on the role of the IGFBP3/TMEM219 apoptotic axis in disease conditions, including intestinal disorders and diabetes, and we describe the advancements in designing and testing novel TMEM219-based targeting approaches in emerging potential clinical applications.

2022-01-01·Advanced Biomedical Research

Expression of Recombinant Insulin-Like Growth Factor-Binding Protein-3 Receptor in Mammalian Cell Line and Prokaryotic (Escherichia coli) Expression Systems

Article

作者: Naseri, Nima ; Mirian, Mina ; Mofid, Mohammad Reza

Background:Insulin-like growth factor binding protein-3 receptor (IGFBP-3R) (Transmembrane protein 219 [TMEM219]) binds explicitly to IGFBP-3 and exerts its apoptotic and autophagy signalling pathway. Constructing a Henrietta Lacks (HeLa) h6-TMEM219 cell characterize the therapeutic potent of TMEM219 that could interrupt the IGFBP-3/TMEM219 pathway, in cancer treatment and destructive cell illnesses such as diabetes and Alzheimer's.Materials and Methods:First, to develop stable overexpressed HeLa h6-TMEM219 cells, and Escherichia coli BL21 (DE3) with high IGFBP-3R expression, the purchased pcDNA3.1-h6-TMEM219 plasmid was transformed and integrated using CaCl2 and chemical transfection reagents, respectively. The pcDNA3.1-h6-TMEM219 transfection and protein expression was evaluated by the polymerase chain reaction (PCR), western blotting, and flow cytometry. Following the induction of h6-TMEM219 expression, a protein was purified using Ni-NTA chromatography and evaluated by the sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE).Results:The 606 base pairs sequence in PCR outcomes confirmed successful pcDNA3.1-h6-TMEM219 transformation in E. Coli BL21 and integration into the HeLa genome. The analysis of protein samples from induced E. Coli BL21 and purified protein demonstrate a band of approximately 22 kDa on SDS-PAGE. Moreover, besides western blot analysis, flow cytometry findings illustrate approximately 84% of transfected HeLa cells (HeLa h6-TMEM219) overexpressed h6-TMEM219 on their surface.Conclusion:We designed a new experiment in the h6-TMEM219 expression procedure in both eukaryotic and prokaryotic hosts. All of our results confirm appropriate transformation and transfection and importantly, approve h6-TMEM 219 membrane expression. Finally, the HeLa h6-TMEM219 cells and the newly purified h6-TMEM219 leverage new studies for molecular diagnostic studies and characterize the therapeutic agents against IGFBP-3/TMEM219 signalling pathway in devastating illnesses in vitro and in vivo.

项与 TMEM219 相关的新闻（医药）

2024-02-20

·entherapharmaceuticals.com

Enthera Pharmaceuticals Will Present Preclinical Data on Ent001, an Anti-TMEM219 Antibody in Development For The Treatment Of Ulcerative Colitis at The European Crohn’s And Colitis Organization 2024 Annual Meeting

Enthera Pharmaceuticals (“Enthera”), a clinical-stage biotech company developing first-in-class antibody therapeutics targeting the Insulin Growth Factor Binding Protein (IGFBP) family for selected inflammatory diseases, confirms its attendance at the European Crohn´s and Colitis Organization – ECCO’24 (ecco-ibd.eu) Conference, scheduled to take place in Stockholm from February 21st to 24th. Enthera will be presenting new preclinical data demonstrating mucosal healing of the GI tract following treatment with our first-in-class anti-TMEM219 monoclonal antibody, Ent001. Enthera will be participating in the guided poster session on Friday, the 23rd of February, where our poster (P171) entitled “Rescuing Intestinal Stem Cells via TMEM219 inhibition promotes mucosal healing in Crohn’s disease” will be showcased. “We are pleased to share the compelling preclinical data with Ent001 in the DSS colitis model that demonstrates significant mucosal healing with both prophylactic and therapeutic dosing regimens. Ent001 offers a potenfial new treatment option for inflammatory bowel disease and is currently being studied in a multiple ascending dose study in ulcerative colitis” said Lisa M. Olson, CEO. About Enthera Pharmaceuticals Enthera Srl is a clinical-stage biotech company developing first-in-class antibody therapeutics to transform the treatment paradigm in inflammatory bowel diseases (IBD) and type 1 diabetes (T1D) by re-establishing stem cell capabilities. Enthera’s pioneering approach capitalizes on the key discovery of the IGFBP3/TMEM219 pathway, which is involved in stem cell and beta cell apoptosis in the gut and pancreas, respectively. Enthera’s lead program, Ent001, which is currently in Phase 1 clinical development, has the potential to restore the original intestinal mucosal structure in IBD and the endogenous pancreatic stem cell compartment in T1D, resulting in the restoration of organ function. Enthera is a private company headquartered in Milan, Italy and founded in 2016 by Prof. Paolo Fiorina and Dr. Francesca D’Addio with BiovelocITA, Italy’s first biotech accelerator. Enthera’s discovery engine and assets are protected by a broad portfolio of patents. The company is backed by Sofinnova Partners, AbbVie Ventures, JDRF T1D Fund, Roche Venture Fund, and several private investors. For further information: www.entherapharmaceuticals.com Enthera Pharmaceuticals Lisa M. Olson Ph.D., CEO info@entherapharmaceuticals.com

临床1期抗体药物偶联物

2023-03-12

·药明康德

治疗脱发的RNAi疗法、有望功能性治愈糖尿病的细胞疗法步入临床... | 一周盘点

▎药明康德内容团队编辑本期看点1. 肿瘤免疫治疗新药Galinpepimut-S联用纳武利尤单抗用于治疗WT1+复发性卵巢癌患者的早期临床数据亮眼，超过90%的患者可产生明确的特异性T细胞反应，患者的一年无进展生存率（PFS）达70%。2. 靶向BCMA的自体CAR-T细胞疗法NXC-201用于治疗多发性骨髓瘤和AL淀粉样变性，总缓解率高达90%和100%。3. 用于治疗雄激素性脱发的RNAi疗法OLX104C进入临床，有望克服全身暴露带来的性功能下降、抑郁等副作用，以及女性患者难以使用的局限性。4. 一款干细胞分化产生的胰岛细胞疗法VX-264进入临床，该疗法具有在不需要使用免疫抑制剂的情况下，功能性治愈1型糖尿病的潜力。药明康德内容团队整理Galinpepimut-S：公布1/2期临床试验数据SELLAS Life Sciences Group公司公布了其靶向WT1蛋白的潜在“first-in-class”肿瘤免疫治疗新药Galinpepimut-S（GPS）联用PD-1抑制剂纳武利尤单抗用于治疗WT1+复发性卵巢癌患者的1期临床数据。该药由4条多肽链构成，抗原表位多达25个，适用于全球范围内绝大多数人类白细胞组织相容性抗原（HLA）类型，能够激发自身免疫系统对WT1抗原强烈的免疫反应。研究结果显示，GPS产生的免疫反应比预期得更广，91%的患者在治疗后产生了明确的WT1特异性T细胞反应。在挽救性化疗后接受两次或两次以上GPS联用纳武利尤单抗治疗作为维持免疫治疗的患者中，接受治疗一年时的PFS为70%。而在没有任何维持治疗的情况下，患者群体的历史一年PFS为55%。此外，数据表明，表达WT1的卵巢癌患者可以获得对GPS免疫治疗的持久反应，从而延缓可测量的疾病复发。这与单独的挽救性化疗形成鲜明对比，后者通常会产生短暂的反应然后迅速复发，并需要接受后续治疗，这意味着患者的结局更差、累积毒性的负担增加。NXC-201：公布1b/2a期临床试验的新数据Nexcella公司公布了其靶向BCMA的自体CAR-T细胞疗法NXC-201的1b/2a期临床试验的新数据。该研究旨在评估NXC-201用于治疗复发/难治性多发性骨髓瘤和AL淀粉样变性的安全性和有效性。截至2022年10月23日的数据，NXC-201在复发/难治性多发性骨髓瘤患者中表现出潜在有意义的疗效和持久的反应。在42例接受2期临床推荐剂量（RP2D）NXC-201的多发性骨髓瘤患者中，观察到的总缓解率（ORR）为90%，完全缓解（CR）率为59%。在5例接受NXC-201治疗的复发/难治性AL淀粉样变性患者中，产生了100%的ORR和100%的器官缓解率。此外，NXC-201的耐受性良好，42例可评估的患者中未观察到免疫效应细胞相关神经毒性综合征（ICANS），观察到的细胞因子释放综合征（CRS）均可控。OLX104C：IND申请获得澳大利亚人类研究伦理委员会许可OLX104C是Olix pharmaceuticals公司基于其不对称siRNA（cp-asiRNA）平台开发的以雄激素受体（AR）为靶点的RNAi疗法，用于治疗雄激素性脱发。雄激素性脱发是男性荷尔蒙睾酮被5α-还原酶（5-alpha reductase）转化为二氢睾酮（DHT）后，DHT与AR的结合引起的，这会影响毛囊，导致头皮前部和头顶部位的毛发逐渐变短变细，最终引起脱发。该疗法通过局部注射到头皮，只会在脱发部位维持高浓度，进入血液后会迅速分解，因此有望克服全身暴露带来的性功能下降、抑郁等副作用，以及女性患者难以使用的局限性。VX-264：IND申请获得FDA许可VX-264是Vertex Pharmaceuticals公司开发的一款干细胞分化产生的胰岛细胞疗法，旨在治疗1型糖尿病。1型糖尿病患者由于免疫系统破坏了胰腺中产生胰岛素的胰岛细胞，从而导致胰岛素产生减少和高血糖。VX-264是一种细胞疗法和医疗器械的组合，将VX-880封装在Vertex开发的医疗器械中。这一装置可以通过手术植入到患者体内，在保护细胞不受免疫排斥的同时，释放细胞生成的胰岛素。2021年，Vertex公司曾公布过其基于干细胞分化的同种异体胰岛细胞疗法VX-880在首位接受治疗的患者中的疗效。在接受单剂VX-880治疗后第90天时，患者恢复胰岛素生产，并且将每天的胰岛素使用量减少了91%。Vertex计划在未来几个月里在1型糖尿病患者中启动1/2期临床试验。EB103：IND申请获得FDA许可EB103是Estrella Biopharma公司利用ARTEMIS技术开发的靶向CD19的T细胞疗法。与传统的CAR-T细胞不同，利用ARTEMIS技术设计的T细胞疗法具有类似TCR-T细胞疗法的天然细胞内调控机制和CAR-T细胞疗法的精准性，有望大幅降低甚至消除与T细胞过度激活相关的CRS及其它与细胞因子相关的副作用。同时通过T细胞表面的共刺激分子协助，可产生足够的T细胞激活信号，促进T细胞活化，强化抗肿瘤效果。由于CD19是一种在几乎所有B细胞白血病和淋巴瘤表面表达的蛋白质，这为Estrella公司启动EB103的1/2期临床试验铺平了道路，有望用于治疗复发或难治性B细胞非霍奇金淋巴瘤（NHL）患者、人类免疫缺陷病毒（HIV）相关淋巴瘤以及原发性和继发性中枢神经系统（CNS）淋巴瘤。AP-PA02：公布1b/2a期临床试验数据Armata Pharmaceuticals公司公布了其新型吸入性多噬菌体疗法AP-PA02的积极早期临床结果。该疗法可以通过雾化有效地输送到肺部，用于治疗囊性纤维化患者的慢性肺铜绿假单胞菌感染。此次公布的数据显示，AP-PA02的耐受性良好，治疗伴发不良反应（TEAE）的特征与安慰剂相似。该候选疗法的全身暴露量小，单次剂量递增与多次剂量递增研究中对诱导痰液进行了检测，发现其暴露量成比例增加，表明其药代动力学是可预测的。研究人员在几个时间点测量了受试者痰液中铜绿假单胞菌的细菌水平，并与给药前的基线水平进行了比较。结果表明，给药10天后，接受AP-PA02治疗的受试者与安慰剂组患者相比，在治疗结束时细菌载量的减少有所改善。MT-8421：IND申请获得FDA许可MT-8421是Molecular Templates公司利用其专有的药物平台开发的靶向CTLA-4的工程化毒素体（Engineered Toxin Bodies，ETBs），用于治疗先前接受过检查点抑制剂的复发/难治性实体肿瘤患者。MT-8421以一种与当前的单克隆抗体完全不同的方式靶向CTLA-4，旨在通过直接的细胞杀伤机制消除肿瘤微环境（TME）中表达CTLA-4的调节性T细胞（免疫抑制性调节性T细胞），该机制独立于抗体所依赖的效应细胞的存在，同时不影响外围的调节性T细胞。临床前数据显示，在表达人CTLA-4并携带同系皮下肿瘤的转基因小鼠模型中，MT-8421治疗消耗了TME中的免疫抑制性调节性T细胞，同时不影响外围的调节性T细胞。该公司预计将在2023年年中启动MT-8421的首次人体1期研究。RLYB212：公布1b期临床试验的新数据Rallybio Corporation公司公布了RLYB212的1b期临床试验的新结果。RLYB212是一种用于预防胎儿和新生儿同种免疫性血小板减少症（FNAIT）的抗人类血小板抗原1a（HPA-1a）单克隆抗体。FNAIT是一种由于准妈妈和她的胎儿的HPA-1特定血小板抗原免疫不相容导致的罕见疾病，母亲体内产生的抗HPA-1a抗体可以穿过胎盘并破坏胎儿的血小板，可能导致包括流产、死产、新生儿死亡或存活婴儿的严重终生神经功能障碍在内的多种严重后果。目前尚无批准用于预防或治疗FNAIT的疗法。此次公布的新数据表明，在严重胎儿母体出血的模型中，单次皮下给药一周后，两种剂量的RLYB212相比于安慰剂都能够更迅速地消除输注的HPA-1a阳性血小板，平均血小板消除半衰期减少了90%以上，且呈剂量相关性。此外，RLYB212的耐受性良好，无严重不良事件（SAE）。HMBD-001：启动1/2a期临床试验HMBD-001是Hummingbird Bioscience公司开发的靶向HER3的IgG1抗体，用于治疗对获批疗法耐药的实体肿瘤患者。该候选疗法有可能通过靶向位于HER3与HER2或EGFR形成异二聚体的连接处的关键表位，完全阻断配体依赖性和非依赖性HER3激活和致癌信号。在临床前模型中，该公司观察到HMBD-001与现有的HER3抗体相比具有更好的亲和力和更有效的肿瘤生长抑制作用。Ent001：启动1期临床试验Ent001是Enthera Pharmaceuticals公司开发的一种靶向IGFBP3/TMEM219通路的单克隆抗体，该通路在炎症性肠病和1型糖尿病中起关键作用。高水平的IGFBP3与TMEM219受体结合，将导致结肠干细胞和胰腺中产生胰岛素的β细胞凋亡。Ent001旨在与TMEM219结合以阻止细胞死亡和这些疾病状态背后的炎症的发生。该候选疗法的随机、双盲、安慰剂对照的单次递增剂量1期试验将在荷兰开展，以评估Ent001在30名健康成年受试者中的安全性、药代动力学（PK）、药效学（PD）以及免疫原性。FRTX-02：公布1期临床试验数据Fresh Tracks Therapeutics公布了其强效、高选择性、潜在“first-in-class”的口服DYRK1A抑制剂FRTX-02的1期临床试验数据。该试验旨在评估FRTX-02在健康受试者和特应性皮炎患者中的安全性、耐受性、药代动力学和药效学。研究结果显示，FRTX-02在潜在治疗剂量范围内通常是安全的，且耐受性良好，符合研究的主要目标；潜在治疗剂量范围内的血浆浓度与非临床疾病模型中建立的有效暴露水平一致，支持每日一次口服给药；在探索性离体LPS刺激的全血药效学测定中观察到疾病相关细胞因子的减少。该结果支持FRTX-02作为特应性皮炎和/或其他自身免疫性疾病的潜在“first-in-class“治疗。大家都在看药明康德为全球生物医药行业提供一体化、端到端的新药研发和生产服务，服务范围涵盖化学药研发和生产、生物学研究、临床前测试和临床试验研发、细胞及基因疗法研发、测试和生产等领域。如您有相关业务需求，欢迎点击下方图片填写具体信息。▲如您有任何业务需求，请长按扫描上方二维码，或点击文末“阅读原文/Read more”，即可访问业务对接平台，填写业务需求信息▲欲了解更多前沿技术在生物医药产业中的应用，请长按扫描上方二维码，即可访问“药明直播间”，观看相关话题的直播讨论与精彩回放参考资料（可上下滑动查看）[1] Armata Pharmaceuticals Announces Positive Topline Data from Phase 1b/2a SWARM-P.a. Clinical Trial of Inhaled AP-PA02 in Patients with Cystic Fibrosis. Retrieved March 10, 2023, from https://www.prnewswire.com/news-releases/armata-pharmaceuticals-announces-positive-topline-data-from-phase-1b2a-swarm-pa-clinical-trial-of-inhaled-ap-pa02-in-patients-with-cystic-fibrosis-301762961.html[2] Rallybio Announces Proof-of-Concept Achieved for RLYB212, a Novel Monoclonal anti-HPA-1a Antibody to Prevent Fetal and Neonatal Alloimmune Thrombocytopenia. Retrieved March 10, 2023, from https://www.businesswire.com/news/home/20230302005706/en[3] Hummingbird Bioscience Exercises Its Option to License the Clinical Trial Results from Cancer Research UK to Support Further Development of HMBD-001. Retrieved March 10, 2023, from https://www.prnewswire.com/news-releases/hummingbird-bioscience-exercises-its-option-to-license-the-clinical-trial-results-from-cancer-research-uk-to-support-further-development-of-hmbd-001-301763185.html[4] Nexcella to Discuss Recent Positive NXC-201 Clinical Data In AL Amyloidosis and Multiple Myeloma at the 35th Annual Roth Conference on March 14. Retrieved March 10, 2023, from https://www.nexcella.com/2023/03/06/nexcella-to-discuss-recent-positive-nxc-201-clinical-data-in-al-amyloidosis-and-multiple-myeloma-at-the-35th-annual-roth-conference-on-march-14/[5] Fresh Tracks Therapeutics Announces Positive Topline Results from Single and Multiple Ascending Dose Parts of Phase 1 Study of Oral DYRK1A Inhibitor FRTX-02. Retrieved March 10, 2023, from https://ir.frtx.com/news/detail/95/fresh-tracks-therapeutics-announces-positive-topline[6] SELLAS Announces Publication of Positive GPS Clinical Data in Ovarian Cancer in Peer Reviewed Journal. Retrieved March 10, 2023, from https://www.sellaslifesciences.com/investors/news/News-Details/2023/SELLAS-Announces-Publication-of-Positive-GPS-Clinical-Data-in-Ovarian-Cancer-in-Peer-Reviewed-Journal/default.aspx[7] Indaptus Therapeutics Doses First Subject in its Ongoing Phase 1 Open Label Clinical Trial of Decoy20 in Patients with Advanced Solid Tumors. Retrieved March 10, 2023, from https://indaptusrx.com/investors/news-releases/[8] Enthera Pharmaceuticals Initiates Phase 1 Clinical Trial with Lead Candidate Ent001. Retrieved March 10, 2023, from https://www.businesswire.com/news/home/20230307005122/en/[9] Estrella Biopharma Announces FDA Clearance of IND Application for Phase I/II Clinical Trial (Starlight-1) of EB103, a CD19-Targeted ARTEMIS® T Cell Therapy, to Patients with B-Cell Lymphomas. Retrieved March 10, 2023, from https://www.prnewswire.com/news-releases/estrella-biopharma-announces-fda-clearance-of-ind-application-for-phase-iii-clinical-trial-starlight-1-of-eb103-a-cd19-targeted-artemis-t-cell-therapy-to-patients-with-b-cell-lymphomas-301766225.html[10] QSAM Biosciences Receives Clearance from FDA to Expand Enrollment Criteria in its Phase 1 Study of CycloSam® Targeting Metastatic Bone Cancer. Retrieved March 10, 2023, from https://www.globenewswire.com/news-release/2023/03/08/2622983/0/en/QSAM-Biosciences-Receives-Clearance-from-FDA-to-Expand-Enrollment-Criteria-in-its-Phase-1-Study-of-CycloSam-Targeting-Metastatic-Bone-Cancer.html[11] Molecure announces first patient dosed in Phase I trial with novel, first-in-class dual arginase inhibitor OATD-02 for the treatment of cancer. Retrieved March 10, 2023, from https://molecure.com/molecure-announces-first-patient-dosed-in-phase-i-trial-with-novel-first-in-class-dual-arginase-inhibitor-oatd-02-for-the-treatment-of-cancer/[12] 올릭스, ‘AR asiRNA’ ‘탈모 1상 “호주 IND 승인”. Retrieved March 10, 2023, from http://biospectator.com/view/news_view.php?varAtcId=18457[13] Vertex Announces FDA Clearance of Investigational New Drug Application for VX-264, a Novel Encapsulated Cell Therapy for the Treatment of Type 1 Diabetes. Retrieved March 9, 2023, from https://www.businesswire.com/news/home/20230308005894/en/Vertex-Announces-FDA-Clearance-of-Investigational-New-Drug-Application-for-VX-264-a-Novel-Encapsulated-Cell-Therapy-for-the-Treatment-of-Type-1-Diabetes[14] Molecular Templates Announces IND Acceptance by FDA for MT-8421 ETB Program Targeting CTLA-4. Retrieved March 9, 2023, from https://www.globenewswire.com/news-release/2023/03/09/2624321/0/en/Molecular-Templates-Announces-IND-Acceptance-by-FDA-for-MT-8421-ETB-Program-Targeting-CTLA-4.html[15] Ribon Therapeutics Doses First Patient in Phase 1 Clinical Study with RBN-3143 in Patients with Moderate-to-Severe Atopic Dermatitis. Retrieved March 9, 2023, from https://www.businesswire.com/news/home/20230309005186/en/[16] BerGenBio Announces First Patient Dosed in Phase 1b/2a Trial Evaluating Bemcentinib in 1st Line Non-Small Cell Lung Cancer with STK11 Mutations. Retrieved March 9, 2023, from https://www.prnewswire.com/news-releases/bergenbio-announces-first-patient-dosed-in-phase-1b2a-trial-evaluating-bemcentinib-in-1st-line-non-small-cell-lung-cancer-with-stk11-mutations-301767793.html免责声明：药明康德内容团队专注介绍全球生物医药健康研究进展。本文仅作信息交流之目的，文中观点不代表药明康德立场，亦不代表药明康德支持或反对文中观点。本文也不是治疗方案推荐。如需获得治疗方案指导，请前往正规医院就诊。版权说明：本文来自药明康德内容团队，欢迎个人转发至朋友圈，谢绝媒体或机构未经授权以任何形式转载至其他平台。转载授权请在「药明康德」微信公众号回复“转载”，获取转载须知。分享，点赞，在看，聚焦全球生物医药健康创新

免疫疗法细胞疗法临床1期临床2期临床结果

2023-03-07

·BioSpace

Enthera Pharmaceuticals Initiates Phase 1 Clinical Trial with Lead Candidate Ent001

Phase 1 study in healthy volunteers lays groundwork for Ent001 evaluation in patients with inflammatory bowel disease and type 1 diabetes MILAN--(BUSINESS WIRE)-- Enthera Pharmaceuticals (“Enthera”), a biotech company developing first-in-class biologics for selected autoimmune conditions, today announces the start of a Phase 1 first-in-human (FIH) clinical trial with its lead candidate Ent001. Ent001 is a monoclonal antibody (mAb) targeting the IGFBP3/TMEM219 pathway, which plays a critical role in both inflammatory bowel disease (IBD) and type 1 diabetes (T1D). Elevated levels of IGFBP3 bind to the TMEM219 receptor, causing apoptosis of both colonic stem cells in the gut and insulin-producing beta cells in the pancreas. Ent001 is designed to bind to TMEM219 and prevent cell death and the inflammation underlying these disease states. The trial in healthy volunteers will evaluate Ent001’s safety and tolerability and establish optimal dose levels for subsequent trials in patients with IBD and T1D, the target indications for the next stage of Ent001’s clinical development. “The initiation of this trial is a major development milestone for Ent001 and transitions Enthera into a clinical stage company. The data we gather from this study will be instrumental to optimize the development of our lead candidate and enable future development in IBD and T1D,” said Aled Paton Williams, CEO of Enthera. The Phase 1 trial will evaluate Ent001 in up to 30 healthy adult volunteers in a randomised, double-blind, placebo-controlled single ascending dose (SAD) study in the Netherlands. In addition to safety, the trial will assess Ent001’s pharmacokinetics, pharmacodynamics, and immunogenicity. “This trial builds on our robust preclinical data that revealed a strong safety pro demonstrated noteworthy results with Ent001’s unique mode of action in well-established animal disease models. We look forward to applying our unique understanding of the recently discovered IGFBP3/TMEM219 axis to establish Ent001’s potential as a first-in-class therapeutic with the ability to halt and reverse disease progression in IBD and T1D,” said Filippo Canducci, Chief Medical Officer of Enthera. About Enthera Pharmaceuticals Enthera Srl is a biotech company developing first-in-class biologics to transform the treatment paradigm for specific autoimmune conditions by preserving and re-establishing cell and organ function. The Company’s primary target indications are inflammatory bowel disease (IBD) and type 1 diabetes (T1D). Enthera’s pioneering approach capitalizes on the key discovery of the IGFBP3/TMEM219 pathway, which is involved in stem cell and beta cell apoptosis in the gut and pancreas, respectively. Enthera is a private company headquartered in Milan, Italy, and founded in 2016 by Prof. Paolo Fiorina and Dr. Francesca D’Addio at BiovelocITA, Italy’s first biotech accelerator. The Company is backed by Sofinnova Partners, AbbVie INC, JDRF T1D Fund, Roche Finance LTD and a number of private investors. Enthera’s discovery engine and assets are protected by a broad portfolio of patents. For further information: View source version on businesswire.com: Contacts Enthera Pharmaceuticals Aled Williams, CEO info@entherapharmaceuticals.com Trophic Communications Valeria Fisher or Veronika Máté +49 175 8041816 or +49 160 90816161 enthera@trophic.eu Source: Enthera View this news release online at:

临床1期