A Phase II Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of SHR1459 Tablets in the Treatment of Primary Membranous Nephropathy (PMN)

The purpose of this study is to evaluate the efficacy and safety of SHR1459 tablets in patients with primary membranous nephropathy.

开始日期2021-12-15

申办/合作机构

瑞石生物医药有限公司

100 项与 Edralbrutinib 相关的临床结果

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100 项与 Edralbrutinib 相关的转化医学

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100 项与 Edralbrutinib 相关的专利（医药）

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项与 Edralbrutinib 相关的文献（医药）

2024-12-17·ACS Omega

Structure-Based QSAR Modeling of RET Kinase Inhibitors from 49 Different 5,6-Fused Bicyclic Heteroaromatic Cores to Patent-Driven Validation

Article

作者: Jin, Sumin ; Kumar, Surendra ; Kim, Mi-hyun

RET receptor tyrosine kinase is crucial for nerve and tissue development but can be an important oncogenic driver. This study focuses on exploring the design principles of potent RET inhibitors through molecular docking and 3D-QSAR modeling of 5,6-fused bicyclic heteroaromatic derivatives. First of all, RET inhibitors of 49 different bicyclic substructures were collected from five different data sources and selected through molecular docking simulations. QSAR models were built from the 3399 conformers of 952 RET inhibitors using the partial least-squares method and statistically evaluated. The optimal QSAR model exhibited high predictive performance, with R ² (of training data) and Q ² (of test data) values of 0.801 and 0.794, respectively, effectively predicting known inhibitors. The optimal model was doubly verified by patent-filed RET inhibitors as the out-of-set data to demonstrate acceptable residual analysis results. Moreover, feature importance analysis of the QSAR model outlined the impact of substituent characteristics on the inhibitory activity within the 5,6-fused bicyclic heteroaromatic core structures. Furthermore, the relationship between structure and inhibitory activity was successfully applied to the RET screening of known clinical and nonclinical kinase inhibitors to afford accurate off-target prediction.

2021-12-01·Clinical cancer research : an official journal of the American Association for Cancer Research1区 · 医学

Antitumor Activity of the Novel BTK Inhibitor TG-1701 Is Associated with Disruption of Ikaros Signaling in Patients with B-cell Non–Hodgkin Lymphoma

1区 · 医学

Article

作者: Fernández-Serrano, Miranda ; Profitós Pelejà, Núria ; Blecua, Pedro ; Musulen, Eva ; Menéndez, Pablo ; Esteller, Manel ; Ribeiro, Marcelo Lima ; De La Torre, Carolina ; Armengol, Marc ; Bosch, Francesc ; Vinyoles, Meritxell ; Sedó Mor, Alícia ; Santos, Juliana Carvalho ; Normant, Emmanuel ; Roué, Gaël ; Bech-Serra, Joan J. ; Reyes-Garau, Diana ; Miskin, Hari

Abstract:

Purpose::

Despite the remarkable activity of BTK inhibitors (BTKi) in relapsed B-cell non–Hodgkin lymphoma (B-NHL), no clinically-relevant biomarker has been associated to these agents so far. The relevance of phosphoproteomic profiling for the early identification of BTKi responders remains underexplored.

Experimental Design::

A set of six clinical samples from an ongoing phase I trial dosing patients with chronic lymphocytic leukemia (CLL) with TG-1701, a novel irreversible and highly specific BTKi, were characterized by phosphoproteomic and RNA sequencing (RNA-seq) analysis. The activity of TG-1701 was evaluated in a panel of 11 B-NHL cell lines and mouse xenografts, including two NF-κB- and BTKC481S-driven BTKi-resistant models. Biomarker validation and signal transduction analysis were conducted through real-time PCR, Western blot analysis, immunostaining, and gene knockout (KO) experiments.

Results::

A nonsupervised, phosphoproteomic-based clustering did match the early clinical outcomes of patients with CLL and separated a group of “early-responders” from a group of “late-responders.” This clustering was based on a selected list of 96 phosphosites with Ikaros-pSer442/445 as a potential biomarker for TG-1701 efficacy. TG-1701 treatment was further shown to blunt Ikaros gene signature, including YES1 and MYC, in early-responder patients as well as in BTKi-sensitive B-NHL cell lines and xenografts. In contrast, Ikaros nuclear activity and signaling remained unaffected by the drug in vitro and in vivo in late-responder patients and in BTKC481S, BTKKO, and noncanonical NF-κB models.

Conclusions::

These data validate phosphoproteomic as a valuable tool for the early detection of response to BTK inhibition in the clinic, and for the determination of drug mechanism of action.

项与 Edralbrutinib 相关的新闻（医药）

2025-01-07

·CPHI制药在线

潜力蓝海赛道，跑出国产创新药黑马

关注并星标CPHI制药在线近段时间，国内药企云顶新耀传来好消息，其创新药EVER001胶囊在治疗原发性膜性肾病（pMN）的Ib/2a期临床试验中，取得阶段性积极结果。此次EVER001的积极进展具有重要意义，那么其背后有什么特殊背景？什么是膜性肾病？膜性肾病（MN）是成人肾病综合征常见的病理类型，可分为特发性原发性（约占80%病例）和继发性（约占20%病例）两大形式。研究证实，MN是一种针对正常肾小球上皮细胞膜上的抗原成分而产生的自身抗体介导的肾小球损害。其临床特征为水肿、低白蛋白血症和高脂血症等肾病综合征相关症状，同时会增加血栓、感染、心血管疾病等风险。长期未经治疗的患者将有近60%发生肾功能减退，且30-40%将在10年内最终进展为终末期肾病。 MN在我国的患病率正逐年上升，其占比从2001年~2006年的5.5%增长至2013年~2018年的22.5%，已成为仅次于免疫球蛋白A（IgA）肾病的原发性肾小球肾炎。目前，我国约有200万pMN患者，疾病负担远远高于其他国家（美国约有8万-10万患者，欧洲约有8万患者，日本约有4万患者）。对于pMN的治疗，目前主要以缓解蛋白尿等症状的保守治疗为主。对于疾病进展风险高的患者，常采取免疫抑制剂以及联合治疗，包括传统的环磷酰胺、泼尼松及其他皮质激素，以及新型的免疫抑制剂如钙调磷酸酶抑制剂（环孢素和他克莫司）以及CD20单抗（利妥昔单抗等）。但目前这些常用的免疫抑制剂，都处于超适应症应用状态，其安全性和疗效并不尽如人意。究其原因，这与膜性肾病全球暂无获批药物有关。也正因此，目前pMN已是导致透析的第一大原因，占比高达37%，甚至超过糖尿病肾病和高血压肾病透析的总和（约30%）。因此，在膜性肾病赛道，亟需研发能提高治疗缓解率、降低高复发率的治疗药物。 EVER001是赛道黑马吗？云顶新耀的EVER001是一款新一代共价可逆布鲁顿酪氨酸激酶（BTK）抑制剂。BTK是B细胞受体信号通路的重要组成部分，可调节B淋巴细胞的存活、激活、增殖和分化。 I期临床研究证明，EVER001具有高选择性、强效靶点结合能力和良好的安全性特征。在针对以蛋白尿为特征的肾小球疾病患者的Ib/IIa期临床试验中，在已完成36周治疗的低剂量组患者中，81.8%（9/11）的患者实现临床缓解，高剂量组中已完成24周治疗的患者已有85.7%（6/7）实现临床缓解。低剂量组的24小时蛋白尿几何平均值在36周相较于基线下降78.3%，而高剂量组在24周即出现73.8%的下降。在数据截止日，抗-PLA2R（磷脂酶A2受体）自身抗体水平达到接近100%的下降（抗-PLA2R抗体水平和临床疗效紧密相关，其降低预示着临床缓解，尤其是免疫学完全缓解）。与目前指南推荐的利妥昔单抗联合疗法，以及在国内开展的一些研究中，12个月的缓解率在60%左右，部分甚至低至40%相比，EVER001疗效突出。而且EVER001未出现BTK抑制剂典型的不良反应。这对需要长期用药的肾病患者来说，着实难得。而且与通过输液治疗pMN的利妥昔单抗相比，EVER001作为口服小分子化合物，使用更方便。基于以上，EVER001或为pMN赛道黑马，将为全球pMN领域存在的巨大未被满足的临床需求提供解决方案。 MN药物研发现状由于MN患者基数庞大，且现有治疗药物有限，因此，不少药企开始瞄准这一赛道，针对的靶点主要有CD38、BAFF（B 细胞激活因子）、补体CFB/D等。 CD38是一种跨膜糖蛋白，其在多发性骨髓瘤等非实体瘤中的高表达使其成为治疗这些疾病的有效靶点。同时，CD38单抗在自身免疫性疾病治疗中也显示出潜力。 Humanlmmunology Biosciences（以下简称HI-Bio）的Felzartamab是一种靶向CD38的全人源IgG1单克隆抗体，它通过抗体依赖性细胞毒性（ADCC）和抗体依赖性细胞吞噬作用（ADCP）消耗CD38+浆细胞，降低了致病性自身抗体的水平，进而对pMN、IgAN肾病、狼疮性肾炎(LN)等自身免疫性肾脏疾病的治疗产生积极影响。具体来说，Felzartamab可以抑制CD38+浆细胞分泌抗PLA2R自身抗体，减少免疫复合物在足细胞和肾小球基底膜之间的上皮下间隙的沉积，进而对pMN的治疗产生积极影响。 2024年6月6日，渤健和HI-Bio达成协议。根据协议条款，渤健将向HI-Bio支付11.5亿美元预付款(约83亿人民币)，以及6.5亿美元里程碑付款，Felzartamab被渤健收入囊中。 BAFF是一种B细胞稳态调节因子，贝利木单抗（Belimumab）通过靶向 BAFF，可能成为 MN 治疗中的一个新选择。贝利木单抗是一种靶向可溶性BAFF的 IgG-λ单克隆抗体，通过降低PLA2R抗体和诱导缓解在PLA2R阳性MN患者中显示出潜力。值得注意的是，由于膜性肾病发病机制的复杂性，BTK抑制剂较少在该赛道涉足，国内众多在研BTK抑制剂中，仅有恒瑞医药的SHR-1459申报了膜性肾病适应症。截至目前，MN尚无获批的治疗药物，目前使用的治疗手段不仅副作用显著，而且仅有超过30%的患者无效。因此，此次云顶新耀的EVER001取得较为明显的优势，或许能成为MN赛道上一匹国产黑马。主要参考资料： 1. MEENA P, RAMACHANDRAN R, BOSE B, et al. Changing treatment paradigms for membranous nephropathies[J]. Nephrology Dialysis Transplantation, 2024: gfae141. 2. Seifert L, et al. The classical pathway triggers pathogenic complement activation in membranous nephropathy. Nat Commun. 2023 Jan 28;14(1):473. doi: 10.1038/s41467-023-36068-0. PMID: 36709213; PMCID: PMC9884226. 3. 云顶新耀新闻稿 END 【智药研习社近期直播】来源：CPHI制药在线声明：本文仅代表作者观点，并不代表制药在线立场。本网站内容仅出于传递更多信息之目的。如需转载，请务必注明文章来源和作者。投稿邮箱：Kelly.Xiao@imsinoexpo.com ▼更多制药资讯，请关注CPHI制药在线▼ 点击阅读原文，进入智药研习社~

临床结果临床1期临床2期免疫疗法

2024-12-08

·氨基观察

云顶新耀“隐藏金矿”浮现

氨基观察-创新药组原创出品作者 | 蔡九永远不要低估中国创新药企的“韧性”。从2022年低谷至今不到3年时间，云顶新耀股价上涨接近7倍，领涨港股市场。随着依嘉、耐赋康进入放量加速期，基本面持续向上，让市场不断重估云顶新耀的价值。股价上涨的同时，云顶新耀仍在加速创造阿尔法。日前，公司又一座“金矿”浮出水面。 12月4日，云顶新耀公布的数据显示，其BTK抑制剂EVER001胶囊，在治疗原发性膜性肾病的1b/2a期临床试验中显示出积极效果，有潜力成为肾病市场的颠覆者。这也给云顶新耀埋下了价值、估值共同提升的“戴维斯双击”伏笔。价值不难理解。云顶新耀拥有EVER001肾病适应症的全球权益，对应出海预期，价值不容小觑。尤其自去年以来，肾病新药受到追捧，诺华35亿美元收购Chinook、Vertex49亿美元收购Alpine、渤健18亿美元收购HI-Bio，为EVER001的BD价值提供了很好的参考。而估值提升的逻辑，在于云顶新耀战略的推进，从过去的license in到如今的license out，再到接下来的自研管线价值兑现也已经清晰可见。公司不再是市场认为的单纯引进的药企，自然过去的估值逻辑也不再适用。也正因此，在EVER001数据公布后，云顶新耀受到了更多市场机构的认可。日前，中信证券对云顶新耀进行了首次覆盖，认为云顶新耀引进+自研共筑差异化管线的逻辑越来越清晰，后续进展值得期待，对应“买入”评级，2025年目标价为55港元，合理市值为177.68亿港元。不过，当前市场对于云顶新耀的上述预期并未一致形成。但这也意味着，其后续获得更大价值弹性空间的概率，随之放大。 / 01 / 蓝海硬逻辑 EVER001的高价值，与其所处的市场有关。潜在治疗群体规模庞大、临床负担重、有效疗效稀缺，决定了肾病领域是一个超级蓝海市场。以原发性膜性肾病市场为例。作为成人肾病最常见的病理类型，中国原发性膜性肾病患者数近200万例，美国、欧洲、日本等国家总患者病例超20万。原发性膜性肾病会引发肾衰竭。2023年8月份在临床肾病杂志上发表的《Future landscape for the management of membranous nephropathy》显示，如果不治疗，14%的持续性肾病综合征患者在5年时可能发生肾衰竭，35%在10年时发生，41%在15年时发生肾衰竭。遗憾的是，全球没有特效药物获批，临床上主要是以利妥昔超适应症使用为主的治疗手段，局限性明显：大约30%患者没有效果，而有效果的群体中，一半的病人仍患有肾病综合征，1/3的患者仍会进展为终末期肾病。也正因此，目前原发性膜性肾病已是导致透析的第一大原因，占比高达37%，甚至超过糖尿病肾病和高血压肾病透析的总和（约30%）。所以，一款得到临床验证的原发性膜性肾病治疗药物，销售额预期不会太低。而EVER001，不仅能治疗原发性膜性肾病，总共可以治疗4种原发性肾小球肾病，以及继发性狼疮性肾炎。上述适应症潜在群体规模约1000万人，且除了IgA肾病有云顶新耀的耐赋康上市，其他适应症均未有治疗手段获批。因此，EVER001备受市场瞩目。而机制、分子的多重优势，更是赋予其更高的价值期待。作为BTK抑制剂，EVER001作用于疾病发病机制的上游，减少B细胞的活化、增殖和分化，从而减少B细胞产生的自身抗体。除了B细胞，BTK抑制剂还能对多种细胞类型产生免疫调节作用。而目前在肾病领域探索较多的B细胞靶向抗体，包括利妥昔单抗、CD38抗体或BAFF/APRIL抗体等，均只能影响B细胞的特定亚群。同时，EVER001是为数不多的口服小分子药物，进一步提高了“上限”。一方面，为其提供了额外安全性优势，允许在必要时停止治疗，并能使B细胞功能在停药后快速恢复；另一方面，为联合疗法探索提供更多可能。肾病在研疗法较多，不同机制药物或能互补，EVER001安全性良好，且口服带来依从性优势明显，因此未来联用潜力不小。而相比于同类BTK抑制剂，EVER001在分子设计方面具有独特优势。 BTK抑制剂分为三类：共价不可逆、非共价可逆、共价可逆。目前，全球原发性膜性肾病进展较快的BTK抑制剂中，只有EVER001属于共价可逆的设计思路，具备更出色的选择性、更强效靶点结合能力、更少的多脱靶毒性等综合优势。也正因此，EVER001或能带来更大的临床价值，最终体现更高的商业价值。 / 02 / BD预期升温在1b/2a期临床研究中，EVER001秀出了肌肉。根据剂量不同，该研究分为队列1（100mg QD、100mg BID）、队列2（200mg BID）。结果显示，在队列1中，抗-PLA2R抗体水平在第24周时已观察到超过90%的下降；在队列2中，第12周时已观察到90%的下降。抗PLA2R抗体水平和临床疗效紧密相关，其降低预示临床缓解，尤其是免疫学完全缓解。这在患者蛋白尿的下降层面得到了体现。第12周时，两组的蛋白尿基本都下降了30%左右。在快速起效的同时，EVER001展现了极佳的效果。队列2在第24周时，免疫学完全缓解率达到100%，队列1在第36周也达到90%。蛋白尿下降方面，队列1在第36周时下降78.3%，队列2在第24周时下降73.8%。队列1在36周时蛋白尿缓解率达81.8%；队列2在24周时蛋白尿缓解率则达85.7%。作为对比，现在指南推荐的利妥昔单抗联合疗法，在国内开展的一些研究显示，12个月的缓解率在60%左右，部分甚至低至40%。同时，EVER001的疗效还能维持较长的时间。数据显示，不管是队列1和队列2在停药随访期（最长至52周）内，免疫效应均保持稳定。在数据截止日期，两组抗-PLA2R抗体水平下降比例都在100%。效果突出，EVER001的安全性也非常良好。其大多数不良反应为1级或2级，且未观察到传统BTK抑制剂典型的不良反应，也没有严重的肝毒性。不同于肿瘤药物，肾病作为一种需要长期用药的疾病，对安全性的要求更严苛。很显然，良好的安全性，是EVER001的一个加分项。从最新临床数据看，EVER001不仅能显著优于利妥昔等现有药物，还优于潜在的BTK抑制剂竞对，有望更大程度满足原发性膜性肾病市场的临床需求，从而获得巨大的成功。这也预示，EVER001的BD预期要开始升温了。在肾病市场探索的前沿疗法并不少，上文提及的HI-Bio、Chinook、Alpine更是凭借核心管线，收获大药企青睐，创造了多个巨额收购案。这不仅体现了市场对肾病创新疗法价值的高度认可，也将成为EVER001估值的一个重要参考。 / 03 / 估值逻辑重塑 EVER001更是让市场看到，云顶新耀估值重塑的可能。基于稳扎稳打的思路，云顶新耀定下了license in、license out再到自主研发走向全球的循序渐进的战略目标。但license in模式的过于成功，让市场认为云顶新耀只有“引进”逻辑，而忽视了其他的价值。 EVER001最新数据的公布，则展示出公司正加速走向战略的第三阶段，并且有能力兑现所有预期。不只是引进，云顶新耀拥有EVER001在全球范围内开发用于治疗肾病领域的权益。潜台词是，其做到了EVER001在原发性膜性肾病领域从0到1的开发。这并不容易。因为该病患者对治疗的反应存在很大的异质性，加上长期管理和预后难度较大，研发难度极高。也正因此，肾病是BTK抑制剂较少涉足的领域。Insight数据库显示，2021年9月份云顶新耀踏入该领域之时，国内22款BTK抑制剂中仅恒瑞医药的SHR-1459申报了膜性肾病。可以说，EVER001在原发性膜性肾病领域的研发，是云顶新耀完全基于自己的理解和探索、实践，最终实现“破冰”，这验证了其全面的R&D能力，不存在研发短板。因此，云顶新耀有能力继续拓展新分子和开发新适应症，保证其在肾病，以及更多领域的布局持续深入，带来更多高价值的“全球权益”产品。而公司过往突出的前瞻布局能力，更是保证了这一点。过去很长一段时间，由于机制复杂、临床周期较长，肾病一直都是冷门领域。传统的肾脏病临床研究将死亡、终末期肾病等“硬”终点作为主要评估指标，面临长时间随访等综合痛点，一定程度上造成了肾病高质量的临床试验相对较少。但2021年以来，先是KDIGO指南建议将蛋白尿下降指标作为药物缓解IgA肾病进展的合理替代终点，又是耐赋康成为FDA首个基于蛋白尿下降的替代临床终点批准首款IgA肾病药物，预示了肾病的研发门槛大幅降低。也正因此，近年来肾病市场才会呈现火热的趋势。而云顶新耀则做到了提早布局、完成卡位，证明了管理层的过人之处。这背后，得益于公司打造了成功的作战体系。在特定疾病领域，云顶新耀通常会通过自有的顶尖科研团队组合全球资源，构筑从研发、临床甚至后续全球商业化运作的能力。正因此，在肾病领域，云顶新耀的理解绝对是行业领先的，这保证了公司能够不断挖掘肾病领域的潜力分子，并制定合适的临床策略，确保研发成果的转化，实现全球价值最大化。在电话会议上，公司表示，未来将会基于获益维度考虑，推进EVER001相应的国际化工作。可以说，EVER001的突围，看似偶然，实则必然。未来，云顶新耀在研发、出海层面会给市场带来更多惊喜。这个过程，也将伴随着公司估值逻辑的切换。 / 04 / 总结春天的希望总是在寒冬中埋下，伟大的变革通常源于至暗时刻。过去几年，中国创新药行业的发展超出所有人预料。环境的突然变化，打了很多药企一个措手不及，云顶新耀也一度未达市场预期，股价跌至冰点。但也恰恰是在过去几年应对极端挑战时的思考和播种，推动了公司的脱胎换骨。 2022年9月，随着罗永庆加入，云顶新耀开启一系列战略改革。一方面，捋顺了“聚焦蓝海+双轮驱动”的高效战略打法，完成肾病、抗感染和自免等领域的布局，同时强化自研和mRNA技术平台布局。另一方面，推动公司文化重塑，凝聚人心、提升战斗力。得益于此，云顶新耀快速迎来了新生，2023年至今3款商业化产品上市，如今“双轮驱动”的模式也即将进入收获期。可以说，虽然在2022年之前交了一笔学费，但公司却获得了穿越周期的能力，也成功重新赢回了市场的认可。今年以来，其股价涨幅超120% 能够在动荡中不断重塑自我，预示着云顶新耀未来的路会越走越宽。这不仅是云顶新耀的故事，也是中国创新药产业的根本逻辑。 PS：欢迎扫描下方二维码，添加氨基君微信号交流。

并购临床研究引进/卖出临床2期

2024-09-19

·PRNewswire

Mantle Cell Lymphoma Clinical Trial Pipeline Insights Featuring 20+ Companies | DelveInsight

Mantle cell lymphoma is a rare and aggressive type of non-Hodgkin lymphoma originating from B-cells in the "mantle zone" of the lymph nodes. The development of novel targeted therapies and immunotherapies, such as Bruton's tyrosine kinase (BTK) inhibitors, is improving treatment outcomes and driving market growth for Mantle cell lymphoma. LAS VEGAS, Sept. 19, 2024 /PRNewswire/ -- DelveInsight's ' Mantle Cell Lymphoma Pipeline Insight 2024 ' report provides comprehensive global coverage of pipeline mantle cell lymphoma therapies in various stages of clinical development, major pharmaceutical companies are working to advance the pipeline space and future growth potential of the mantle cell lymphoma pipeline domain. Key Takeaways from the Mantle Cell Lymphoma Pipeline Report DelveInsight's mantle cell lymphoma pipeline report depicts a robust space with 20+ active players working to develop 22+ pipeline therapies for mantle cell lymphoma treatment. Key mantle cell lymphoma companies such as AbbVie, Adicet Bio, InnoCare Pharma Inc., Guangzhou Lupeng Pharmaceutical Company LTD., BeiGene, Nurix, LegoChem Biosciences, Xynomic Pharmaceuticals, Merck & Co, Incyte Corporation, TG Therapeutics, Janssen/Pharmacyclics, Eternity Bioscience, Traws Pharm, Advenchen Laboratories, and others are evaluating new mantle cell lymphoma drugs to improve the treatment landscape. Promising mantle cell lymphoma pipeline therapies such as Venetoclax, ADI-001, Orelabrutinib, LP-168, BGB-11417, NX 2127, LCB 71, NX 5948, Abexinostat, Pembrolizumab, Parsaclisib, Umbralisib, Ibrutinib, Edralbrutinib, Narazaciclib, Lucitanib, and others are under different phases of mantle cell lymphoma clinical trials. In May 2024, AstraZeneca had announced positive interim results from the Phase III ECHO clinical trial, which evaluated Bruton's tyrosine kinase (BTK) inhibitor Calquence (acalabrutinib) in combination with standard chemoimmunotherapy for treating mantle cell lymphoma (MCL). In March 2024, BeiGene, Ltd. announced the presentation of emerging oncology pipeline data at the American Association for Cancer Research (AACR) Annual Meeting. Additional highlights include preclinical characterization data for an investigational BTK degrader, BGB-16673, currently in clinical development for B-cell malignancies, including mantle cell lymphoma In October 2023, Ascentage Pharma announced that it has entered into a clinical collaboration with AstraZeneca Investment. The two companies will jointly conduct a registrational Phase III study of the Bcl-2 inhibitor, APG-2575 (lisaftoclax), in combination with AstraZeneca's Bruton's tyrosine kinase (BTK) inhibitor, CALQUENCE® (acalabrutinib), in treatment-naive patients with first-line chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL). In January 2023, the FDA granted an orphan drug designation to LP-284, a novel small-molecule, next-generation acylfulvene, for the treatment of mantle cell lymphoma (MCL), a rare and aggressive form of B-cell non-Hodgkin lymphoma (NHL), according to an announcement from Lantern Pharma. Request a sample and discover the recent advances in mantle cell lymphoma treatment drugs @ Mantle Cell Lymphoma Pipeline Report The mantle cell lymphoma pipeline report provides detailed profiles of pipeline assets, a comparative analysis of clinical and non-clinical stage mantle cell lymphoma drugs, inactive and dormant assets, a comprehensive assessment of driving and restraining factors, and an assessment of opportunities and risks in the mantle cell lymphoma clinical trial landscape. Mantle Cell Lymphoma Overview Mantle cell lymphoma (MCL) is a rare subtype of B-cell non-Hodgkin lymphomas (NHLs) characterized by the (11,14) translocation, leading to overexpression of the cyclin D1 (CCND1) gene. Its various morphological variants can make diagnosis challenging, though some cases are straightforward. Many individuals with MCL are asymptomatic in the early stages, but may later seek medical attention due to persistent, typically painless swelling of lymph nodes, especially in the neck and throat region (e.g., Waldeyer's ring). MCL is marked by a reciprocal chromosomal translocation t(11;14)(q13;q32), which places the cyclin D1 gene next to the immunoglobulin heavy chain gene, causing continuous cyclin D1 expression. This overexpression contributes to tumor cell proliferation through cell cycle dysregulation, chromosomal instability, and epigenetic changes. Rarely, MCL cases without this translocation may involve CCND2 or CCND3 translocations. Hypothetical molecular subtypes, based on the cell of origin, correlate with clinical phenotypes: classical or aggressive MCL arises from naive B cells lacking or having limited iGVH mutations and expressing SOX11, a neural transcription factor inhibiting terminal B cell differentiation. The indolent variant originates from antigen-experienced B cells with IGVH somatic hypermutations, typically SOX11-negative and genetically stable. Diagnosis of MCL involves detailed patient history, thorough clinical evaluation, and specialized tests, including biopsy of an affected lymph node or bone marrow. These tests confirm the NHL type and subtype, assess disease extent, and determine appropriate treatments. Treatment for MCL is multifaceted and tailored to each patient, often including chemotherapy, immunotherapy drugs like rituximab, targeted therapies such as ibrutinib, and stem cell transplants, particularly for aggressive disease or younger patients. Radiation therapy may target specific lymphoma areas. Participation in clinical trials can offer new treatment options. Treatment plans are developed collaboratively by healthcare professionals and patients, considering disease stage, overall health, and personal preferences. Regular monitoring and follow-up care are essential to track treatment response and manage side effects effectively. Find out more about mantle cell lymphoma treatment drugs @ Drugs for Mantle Cell Lymphoma Treatment A snapshot of the Mantle Cell Lymphoma Pipeline Drugs mentioned in the report: Learn more about the emerging mantle cell lymphoma pipeline therapies @ Mantle Cell Lymphoma Clinical Trials Mantle Cell Lymphoma Therapeutics Assessment The mantle cell lymphoma pipeline report proffers an integral view of the mantle cell lymphoma emerging novel therapies segmented by stage, product type, molecule type, mechanism of action, and route of administration. Scope of the Mantle Cell Lymphoma Pipeline Report Coverage: Global Therapeutic Assessment By Product Type: Mono, Combination, Mono/Combination Therapeutic Assessment By Clinical Stages: Discovery, Pre-clinical, Phase I, Phase II, Phase III Therapeutics Assessment By Route of Administration: Oral, Parenteral, Intravenous, Subcutaneous, Topical Therapeutics Assessment By Molecule Type: Recombinant fusion proteins, Small molecule, Monoclonal antibody, Peptide, Polymer, Gene therapy Therapeutics Assessment By Mechanism of Action: Apoptosis stimulants, Proto-oncogene protein c-bcl-2 inhibitors, Proteasome inhibitors, Immunologic cytotoxicity, T lymphocyte replacements, Agammaglobulinemia tyrosine kinase inhibitors Key Mantle Cell Lymphoma Companies: AbbVie, Adicet Bio, InnoCare Pharma Inc., Guangzhou Lupeng Pharmaceutical Company LTD., BeiGene, Nurix, LegoChem Biosciences, Xynomic Pharmaceuticals, Merck & Co, Incyte Corporation, TG Therapeutics, Janssen/Pharmacyclics, Eternity Bioscience, Traws Pharm, Advenchen Laboratories, and others Key Mantle Cell Lymphoma Pipeline Therapies: Venetoclax, ADI-001, Orelabrutinib, LP-168, BGB-11417, NX 2127, LCB 71, NX 5948, Abexinostat, Pembrolizumab, Parsaclisib, Umbralisib, Ibrutinib, Edralbrutinib, Narazaciclib, Lucitanib, and others Dive deep into rich insights for new drugs for mantle cell lymphoma treatment, visit @ Mantle Cell Lymphoma Drugs Table of Contents For further information on the mantle cell lymphoma pipeline therapeutics, reach out @ Mantle Cell Lymphoma Treatment Drugs Related Reports B-Cell Lymphoma Epidemiology B-Cell Lymphoma Epidemiology Forecast – 2032 report delivers an in-depth understanding of the disease, historical and forecasted epidemiology as well as the B-cell lymphoma epidemiology trends. B-Cell Lymphoma Market B-Cell Lymphoma Market Insights, Epidemiology, and Market Forecast – 2032 report deliver an in-depth understanding of the disease, historical and forecasted epidemiology, as well as the market trends, market drivers, market barriers, and key B-cell lymphoma companies, including Vincerx Pharma, Ubix Therapeutics, Biomea Fusion Inc, Shanghai Hengrui Pharmaceutical, BeiGene, Hanmi Pharmaceutical, among others. Diffuse Large B-Cell Lymphoma Pipeline Diffuse Large B-Cell Lymphoma Pipeline Insight – 2024 report provides comprehensive insights about the pipeline landscape, pipeline drug profiles, including clinical and non-clinical stage products, and the key DLBCL companies, including Genmab, Roche, Acerta Pharma, Autolus, Xynomic Pharmaceuticals, Genentech, Celgene, AbbVie, Mabion, among others. Diffuse Large B-Cell Lymphoma Market Diffuse Large B-Cell Lymphoma Market Insights, Epidemiology, and Market Forecast – 2034 report deliver an in-depth understanding of the disease, historical and forecasted epidemiology, as well as the market trends, market drivers, market barriers, and key B-cell lymphoma companies, including AbbVie, Genmab, Merck, Roche, Xencor and Janssen, Denovo Biopharma, Calithera Biosciences, IMV, Biogen, Autolus Therapeutics, Allogene Therapeutics, Novartis, Miltenyi Biomedicine, Regeneron Pharmaceuticals, among others. About DelveInsight DelveInsight is a leading Business Consultant and Market Research firm focused exclusively on life sciences. It supports pharma companies by providing comprehensive end-to-end solutions to improve their performance. Get hassle-free access to all the healthcare and pharma market research reports through our subscription-based platform PharmDelve . Contact Us Shruti Thakur [email protected] +14699457679 Logo: SOURCE DelveInsight Business Research, LLP WANT YOUR COMPANY'S NEWS FEATURED ON PRNEWSWIRE.COM? 440k+ Newsrooms & Influencers 9k+ Digital Media Outlets 270k+ Journalists Opted In GET STARTED

临床3期免疫疗法孤儿药

100 项与 Edralbrutinib 相关的药物交易

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适应症	最高研发状态	国家/地区	公司	日期
特发性膜性肾病	临床2期	中国	瑞石生物医药有限公司	2021-12-10
难治性B细胞淋巴瘤	临床2期	中国	江苏恒瑞医药股份有限公司	2021-10-01
弥漫性大B细胞淋巴瘤	临床2期	中国	江苏恒瑞医药股份有限公司	2021-07-09
水通道蛋白4抗体阳性视神经脊髓炎谱系疾病	临床2期	中国	瑞石生物医药有限公司	2020-12-24
复发性B细胞淋巴瘤	临床2期	中国	江苏恒瑞医药股份有限公司	-
膜性肾小球肾炎	临床2期	中国	江苏恒瑞医药股份有限公司	-
视神经脊髓炎	临床2期	中国	江苏恒瑞医药股份有限公司	-
B细胞淋巴瘤	临床1期	澳大利亚	TG Therapeutics, Inc.	2018-09-10
B细胞淋巴瘤	临床1期	波兰	TG Therapeutics, Inc.	2018-09-10
慢性淋巴细胞白血病	临床1期	澳大利亚	TG Therapeutics, Inc.	2018-09-10

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研究	分期	人群特征	评价人数	分组	结果	评价	发布日期


NCT03671590 (TG-1701, ICML2021)	临床1期	B细胞淋巴瘤	123	TG-1701 monotherapy	廠襯簾蓋獵衊鬱鏇鑰範(壓淵膚齋繭艱鏇鑰遞窪) = 構衊構糧遞繭淵餘鹽醖構構糧醖鹽鑰鑰構壓衊 (餘艱夢範醖鏇餘鏇觸獵 ) 更多	积极	2021-06-17
				TG-1701+U2 combination	鹹齋膚淵選醖範廠醖觸(鑰鏇顧窪淵顧選簾糧鏇) = 鏇壓艱鬱餘淵簾艱鹹網膚襯鹹選窪衊衊製艱鹹 (鏇醖鏇夢築鬱鏇範獵鹹 ) 更多
NCT03671590 (TG-1701, EHA2021)	临床1期	慢性淋巴细胞白血病 \| 淋巴瘤	123	TG-1701 monotherapy	選糧膚膚繭遞願廠襯壓(鏇願觸製齋衊範鹹艱鑰) = 糧鹽願網衊鑰襯憲鬱願窪淵廠網繭憲範鬱製壓 (鬱蓋願遞範憲衊窪範醖 ) 更多	-	2021-06-09
				TG-1701+U2 combination	簾觸範觸製築餘襯憲窪(觸廠範糧糧遞齋淵夢蓋) = 範鏇觸糧夢製鬱簾選廠獵齋鑰構艱壓壓願夢憲 (夢壓獵願齋鬱遞願鏇膚 )
NCT03671590 (ASCO2021)	临床1期	慢性淋巴细胞白血病	123	TG-1701 monotherapy	簾窪鏇網範範獵夢艱鬱(網網遞築鏇膚範築衊獵) = TEAEs leading to TG-1701 dose reduction occurred in 6.5% of pts. TEAEs leading to treatment discontinuation occurred in 1.6% of pts (AF, COVID-19) 範膚鏇鬱蓋築顧餘廠衊 (鏇願積糧製鹹遞範齋鏇 )	-	2021-05-28