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Immix Biopharma Doses Additional Patients in Ongoing Phase 1b/2a IMX-110 Monotherapy Clinical Trial

Immix Biopharma Doses Additional Patients in Ongoing Phase 1b/2a IMX-110 Monotherapy Clinical Trial

Immix Biopharma 正在进行的 1b/2a 期 IMX-110 单一疗法临床试验中为更多患者剂量
GlobeNewswire ·  2023/01/13 08:05
  • In January 2023, the 17th new patient was dosed with IMX-110 to date
  • Positive safety data enabled continued dosing of previously enrolled patients
  • Patients undergo CT scans every 8 weeks after dosing to assess tumor response to IMX-110; clinical data expected to be released on a rolling basis beginning in Q1 2023
  • 2023年1月,17个这是到目前为止,新患者服用了IMX-110
  • 积极的安全性数据使先前登记的患者能够继续服药
  • 患者在服药后每8周接受一次CT扫描,以评估肿瘤对IMX-110的反应;临床数据预计将从2023年第一季度开始滚动发布

LOS ANGELES, Jan. 13, 2023 (GLOBE NEWSWIRE) -- Immix Biopharma, Inc. (Nasdaq: IMMX) ("ImmixBio", "Company", "We" or "Us"), a biopharmaceutical company pioneering Tissue-Specific Therapeutics (TSTx)TM targeting oncology and immuno-dysregulated diseases, today announced dosing of an additional patient in its ongoing Phase 1b/2a IMX-110 monotherapy clinical trial.  Positive safety data enabled continued dosing of previously enrolled patients. In January 2023, the seventeenth patient was dosed with IMX-110 to-date. IMX-110 clinical trial data is expected to be released on a rolling basis beginning in Q1 2023; once dosing begins, patients undergo CT scans every 8 weeks to assess tumor response to IMX-110.  "We are delighted with continued robust IMX-110 clinical trial enrollment," said Ilya Rachman, MD PhD, CEO of ImmixBio. "We continue to accumulate valuable clinical data for first-in-class IMX-110 therapy. In Q1 2023 we plan to share clinical data from our IMX-110 monotherapy and IMX-110 combination trial with Beigene/Novartis' anti-PD-1 Tislelizumab."

洛杉矶,2023年1月13日(环球网)--ImMix Biophma,Inc.(纳斯达克代码:IMMX),一家开创组织特异性治疗(TSTx)先河的生物制药公司TM针对肿瘤学和免疫失调疾病的IMX-110公司今天宣布,正在进行的1b/2a期IMX-110单一疗法临床试验中增加了一名患者的剂量。积极的安全性数据使以前登记的患者能够继续服药。2023年1月,第17名患者接受了迄今为止的IMX-110剂量治疗。IMX-110临床试验数据预计将从2023年第一季度开始滚动发布;一旦开始给药,患者每8周进行一次CT扫描,以评估肿瘤对IMX-110的反应。ImMixBio公司首席执行官伊利亚·拉赫曼博士说:“IMX-110临床试验登记人数持续强劲,我们对此感到高兴。我们继续为一流的IMX-110疗法积累有价值的临床数据。我们计划在2023年第一季度分享我们的IMX-110单一疗法和IMX-110与百济神州/诺华公司的抗PD-1 Tislelizumab联合试验的临床数据。

About IMX-110

关于IMX-110

The U.S. Food and Drug Administration ("FDA") approved orphan drug designation ("ODD") for IMX-110 in soft tissue sarcoma. The FDA also approved Rare Pediatric Disease Designation ("RPDD") for IMX-110 for the treatment of rhabdomyosarcoma, a life-threatening form of cancer in children.  RPDD qualifies Immix Biopharma to receive fast track review, and a priority review voucher ("PRV") at the time of marketing approval of IMX-110. PRV holders can benefit from an expedited six-month review of a new drug application for any disease by the FDA.  IMX-110 is currently being evaluated in a phase 1b/2a clinical trial in patients with advanced solid tumors. Learn more at

美国食品和药物管理局(FDA)批准了IMX-110治疗软组织肉瘤的孤儿药物名称(“ODD”)。FDA还批准了IMX-110用于治疗横纹肌肉瘤的罕见儿科疾病指定(RPDD),横纹肌肉瘤是一种威胁儿童生命的癌症。RPDD使ImMix Biophma有资格接受快速通道审查,并在IMX-110上市批准时获得优先审查凭证(PRV)。PRV持有者可以受益于FDA对任何疾病的新药申请进行为期六个月的快速审查。IMX-110目前正在晚期实体肿瘤患者的1b/2a期临床试验中进行评估。了解更多信息

About Immix Biopharma, Inc.

关于ImMix Biophma公司

Immix Biopharma, Inc. (ImmixBio™) (Nasdaq: IMMX) is a clinical-stage biopharmaceutical company pioneering a novel class of Tissue-Specific Therapeutics (TSTx)™ targeting oncology and immuno-dysregulated diseases. Our proprietary SMARxT Tissue-Specific™ Platform produces drug candidates that circulate in the bloodstream, exit through tumor blood vessels and simultaneously attack all 3 components of the tumor micro-environment (TME). We believe ImmixBio's TME Normalization™ technology severs the lifelines between the tumor and its metabolic and structural support. Learn more at

混合生物制药公司(纳斯达克代码:™)是一家临床阶段的生物制药公司,开创了一类针对肿瘤和免疫失调疾病的新型组织特异性治疗(™)药物。我们专有的SMARxT组织特异性™平台生产的候选药物在血液中循环,通过肿瘤血管退出,并同时攻击肿瘤微环境的所有三个组成部分。我们相信,ImMixBio的TME标准化™技术切断了肿瘤与其代谢和结构支持之间的生命线。了解更多信息

Forward Looking Statements

前瞻性陈述

This press release contains "forward-looking statements" Forward-looking statements reflect our current view about future events. When used in this press release, the words "anticipate," "believe," "estimate," "expect," "future," "intend," "plan," or the negative of these terms and similar expressions, as they relate to us or our management, identify forward-looking statements. Such statements, include, but are not limited to, statements contained in this press release relating to our business strategy, our future operating results and liquidity and capital resources outlook. Forward-looking statements are based on our current expectations and assumptions regarding our business, the economy and other future conditions. Because forward–looking statements relate to the future, they are subject to inherent uncertainties, risks and changes in circumstances that are difficult to predict. Our actual results may differ materially from those contemplated by the forward-looking statements. They are neither statements of historical fact nor guarantees of assurance of future performance. We caution you therefore against relying on any of these forward-looking statements. Important factors that could cause actual results to differ materially from those in the forward-looking statements include, without limitation, our ability to raise capital to fund continuing operations; our ability to protect our intellectual property rights; the impact of any infringement actions or other litigation brought against us; competition from other providers and products; our ability to develop and commercialize products and services; changes in government regulation; our ability to complete capital raising transactions; and other factors relating to our industry, our operations and results of operations. Actual results may differ significantly from those anticipated, believed, estimated, expected, intended or planned including: the uncertainties related to market conditions and other factors described more fully in the section entitled 'Risk Factors' in Immix Biopharma's Annual Report on Form 10-K for the year ended December 31, 2021, and other periodic reports filed with the Securities and Exchange Commission. Any forward-looking statements contained in this press release speak only as of the date hereof, and Immix Biopharma, Inc. specifically disclaims any obligation to update any forward-looking statement, whether as a result of new information, future events or otherwise. Factors or events that could cause our actual results to differ may emerge from time to time, and it is not possible for us to predict all of them. We cannot guarantee future results, levels of activity, performance or achievements.

本新闻稿包含“前瞻性陈述”,这些前瞻性陈述反映了我们对未来事件的当前看法。在本新闻稿中使用的“预期”、“相信”、“估计”、“预期”、“未来”、“打算”、“计划”或这些术语的否定或类似表述,当它们与我们或我们的管理层有关时,都是前瞻性陈述。这些陈述包括但不限于本新闻稿中包含的与我们的业务战略、我们未来的经营业绩以及流动性和资本资源前景有关的陈述。前瞻性陈述是基于我们目前对我们的业务、经济和其他未来状况的预期和假设。由于前瞻性陈述涉及未来,它们受到难以预测的内在不确定性、风险和环境变化的影响。我们的实际结果可能与前瞻性陈述中预期的大不相同。它们既不是对历史事实的陈述,也不是对未来业绩的保证。因此,我们提醒您不要依赖这些前瞻性陈述中的任何一项。可能导致实际结果与前瞻性陈述中的陈述大不相同的重要因素包括但不限于我们筹集资本为持续运营提供资金的能力;我们保护我们知识产权的能力;任何针对我们的侵权诉讼或其他诉讼的影响;来自其他供应商和产品的竞争;我们开发产品和服务并将其商业化的能力;政府法规的变化;我们完成融资交易的能力;以及与我们的行业、我们的运营和运营结果相关的其他因素。实际结果可能与预期的、相信的、估计的、预期的大不相同, 预期或计划包括:与市场状况相关的不确定性和在ImMix Biophma截至2021年12月31日的10-K表格年度报告以及提交给美国证券交易委员会的其他定期报告中更全面地描述的其他因素。本新闻稿中包含的任何前瞻性陈述仅代表截至本新闻稿发布之日的情况,ImMix Biophma,Inc.明确表示不承担任何因新信息、未来事件或其他原因而更新任何前瞻性陈述的义务。可能导致我们实际结果不同的因素或事件可能会不时出现,我们不可能预测所有这些因素或事件。我们不能保证未来的结果、活动水平、业绩或成就。

Contacts
Immix Biopharma, Inc.
Gabriel Morris
Chief Financial Officer
ir@immixbio.com
+1 (888) 958-1084

联系人
ImMix Biophma,Inc.
加布里埃尔·莫里斯
首席财务官
邮箱:ir@imMixBio.com
+1 (888) 958-1084


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