A Randomized Double Blind Placebo Controlled Clinical Study to Assess Blood-Derived Autologous Angiogenic Cell Precursor Therapy in Patients With Critical Limb Ischemia (ACP-CLI)

The primary objective of this study is to determine the efficacy and safety of intramuscular injection of ACP-01, comprised of blood-derived autologous ACPs, in subjects with critical limb ischemia who are receiving standard of care therapy and have no endovascular or surgical revascularization options.

开始日期2014-08-01

申办/合作机构

Hemostemix, Inc.

100 项与 ACP-01 相关的临床结果

登录后查看更多信息

100 项与 ACP-01 相关的转化医学

登录后查看更多信息

100 项与 ACP-01 相关的专利（医药）

登录后查看更多信息

项与 ACP-01 相关的文献（医药）

2024-12-01·International Journal of Biological Macromolecules

Separation, purification, structure characterization, and immune activity of a polysaccharide from Alocasia cucullata obtained by freeze-thaw treatment

Article

作者: Qin, Xiangxiang ; Hou, Jiaojiao ; Zhu, Hua ; Gong, Zan ; Zhong, Shian ; Nie, Jing ; Tan, Xiao ; Gong, Huxuan

In this study, ACP-1, a water-soluble polysaccharide was isolated from the roots of Alocasia cucullata (AC) using freeze-thaw treatment (FTT). Structural characterization revealed ACP-1 (2.10×10⁵ Da) to be a homogeneous heteropolysaccharide primarily consisting of glucose, galactose, and arabinose, and a trace of fucose, rhamnose, and glucuronic acid. Methylation analysis and nuclear magnetic resonance spectroscopy revealed that the backbone of ACP-1 consisted of →[3)-β-D-Galp-(1]₄→3,6)-β-D-Glcp-(1→3,6)-β-D-Glcp-(1→, with a branch at C-3. In vitro experiments demonstrated that ACP-1 significantly enhanced the proliferation and phagocytosis of RAW264.7 cells, upregulated the expression of co-stimulatory molecules (CD80 and CD86), and activated RAW264.7 cells via the nuclear factor kappa-B signal transduction pathway, resulting in nitric monoxide release and the secretion of the cytokines tumor necrosis factor-α, interleukin (IL)-1β, and IL-6. Overall, ACP-1 shows potential as a novel immunostimulant.

2013-10-01·Cytotherapy3区 · 医学

Peripheral blood-derived autologous stem cell therapy for the treatment of patients with late-stage peripheral artery disease—results of the short- and long-term follow-up

3区 · 医学

Article

作者: Judit Daróczy ; Gábor Viktor Szabó ; Michael Belkin ; György Acsády ; Zsuzsa Kövesd ; Judit Cserepes

BACKGROUND AIMSRegeneration of the occluded peripheral arteries by autologous stem cell therapy is an emerging treatment modality for no-option patients with peripheral artery disease (PAD). The purpose of this study was to assess safety and efficacy of in vitro-expanded, peripheral blood-derived, autologous stem cells (VesCell) in no-option patients with PAD.METHODSA phase II, open-label, randomized clinical study was performed on 20 patients to investigate the safety and efficacy of VesCell therapy at 1 and 3 months of follow-up. The long-term (2 years) efficacy of the therapy was also evaluated.RESULTSNo side effects of VesCell therapy were found. During the 3 month follow-up in the control group, one death occurred and six major amputations were performed; in the treated group, there were no deaths or major amputations. The difference of limb loss is significant between the two groups. At 2-year follow-up in the control group, two deaths and six major amputations occurred; in the treated group, there were three major amputations. At 3-month follow-up, the change in hemodynamic parameters showed a significant increase in the treated group over the control group; in the treated group, further improvement was detected at 2 years. As the result of the VesCell treatment, change in pain score, wound healing and walking ability test showed an improvement compared with the control group; at 2 years, incremental improvement was observed.CONCLUSIONSPeripheral blood-derived, in vitro-expanded autologous angiogenic precursor therapy appears to be a safe, promising and effective adjuvant therapy for PAD patients.

2006-10-01·Clinical and Experimental Medicine3区 · 医学

Aneuploidy of chromosome 8 detected by fluorescence in situ hybridisation in ACP01 cell line gastric adenocarcinoma

3区 · 医学

Article

作者: L. Gonçalves Quintana ; M. Ferreira Leal ; S. Satomi Takeno ; R. Rodríguez Burbano ; A. Costa Guimarães ; P. Pimentel Assumpção ; M. de Arruda Cardoso Smith ; E. Suchi Chen ; E. Moura Lima ; A. Salim Khayat

Gastric cancer is the third most frequent type of neoplasia and the second most important cause of death in the world. ACP01 is the first gastric adenocarcinoma cell line developed in Brazil. To evaluate chromosomal aberrations implicated in gastric carcinogenesis, we analysed three different passages (6th, 12th and 35th) of ACP01 cell line by fluorescence in situ hybridisation using chromosome 8 alpha-satellite probe. Most of the chromosome 8 alterations found involved a numerical increase of this chromosome. Chromosome 8 trisomy was detected in all cases, varying from 37% (6th passage) to 67% (35th passage), and chromosome 8 tetrasomy (also observed in all passages) varied from 2.5% (6th passage) to 30% (35th passage). The presence of five signals for chromosome 8 was observed in all passages with the highest frequency found in the 12th passage (20%). Our results confirm that trisomy of chromosome 8 is a common biological phenomenon in adenocarcinoma of stomach and can be used as a gastric mucosa malignancy marker. Although gastric tumours are frequent neoplasias, papers on their cytogenetics are scarce in the literature. It is, therefore, necessary to conduct new studies aiming to identify peculiar genetic characteristics of a tumour, which might help in diagnosis and prognosis of this disease, besides allowing more accurate therapeutic conduct to be established.

项与 ACP-01 相关的新闻（医药）

2024-11-07

·ioncology

2024 ASH大会摘要公布！70+篇中国学者研究入选口头报告，创历史新高！

编者按第66届美国血液学会（ASH）将于2024年12月7～10日在美国圣迭戈（San Diego）盛大召开。作为全球血液学领域规模最大、涵盖最全面的国际学术盛会之一，每年吸引着成千上万名来自世界各地的专家学者，分享最前沿的血液学进展和突破性临床数据。日前，大会官网公布了入选摘要，引人瞩目的是，70+篇由中国学者主导的研究入选口头报告（Oral），创历史新高！这些研究成果不仅是血液学领域探索的最前沿标志，更彰显了中国在血液学研究版图上的坚实步伐与卓越贡献。本刊特此精心整理，带您领略中国血液学专家的非凡风采与卓越成就。恶性血液肿瘤篇 PART.01 01 摘要号：38 标题：The TFG-ROS1 Fusion Is an Oncogenic Driver of Human Myeloid Leukemia 中文标题：TFG-ROS1融合是人类髓系白血病的一个致癌驱动因素汇报人：Jie Sun（浙江大学医学院附属第一医院骨髓移植中心）汇报时间：Saturday, December 7, 2024: 9:45 AM汇报地点：Room 6A （San Diego Convention Center） 02 摘要号：89 标题：Targeted-Delivery Strategy of Engineered EV Functionalized By Anti-CD3/CD19 Bi-Specific T-Cell Engager in Treating B-Cell Malignancies 中文标题：抗CD3/CD19双特异性T细胞衔接器功能化EV治疗B细胞恶性肿瘤的靶向递送策略汇报人：Xiuiu Yang（华中科技大学同济医学院同济医院血液科）汇报时间：Saturday, December 7, 2024: 10:30 AM汇报地点：Ballroom 20AB （San Diego Convention Center） 03 摘要号：91 标题：Rituximab, Lenalidomide, and Zanubrutinib （ZR2） with Sequential CAR-T Cell As First-Line Therapy for High-Risk Large B Cell Lymphoma 中文标题：利妥昔单抗联合来那度胺和泽布替尼（ZR2）序贯CAR-T细胞疗法作为高危大B细胞淋巴瘤的一线治疗汇报人：Mingming Zhang（浙江大学医学院附属第一医院骨髓移植中心）汇报时间：Saturday, December 7, 2024: 9:30 AM 汇报地点：Marriott Grand Ballroom 11-13（Marriott Marquis San Diego Marina） 04 摘要号：92 标题：IL-10 Expressing CD19 CAR-T Cells Induce Complete Remission and Improve Long-Term Protection in Relapsed or Refractory B-Cell Hematological Malignancies 中文标题：表达IL-10的CD19 CAR-T细胞诱导复发或难治性B细胞血液恶性肿瘤完全缓解并改善长期保护作用汇报人：Jingjing Ren（深圳市莱芒生物科技有限公司）汇报时间：Saturday, December 7, 2024: 9:45 AM汇报地点：Marriott Grand Ballroom 11-13 （Marriott Marquis San Diego Marina） 05 摘要号：156 标题：Potent in Vitro and In Vivo Efficacy of Hdz-C123A, a GSPT1 Degrader-Antibody Conjugate Targeting CD123 in Acute Myeloid Leukemia 中文标题：靶向CD123的GSPT1降解抗体偶联物Hdz-C123A在急性髓系白血病中的体外和体内疗效汇报人：Yu Guo（杭州和正医药有限公司）汇报时间：Saturday, December 7, 2024: 1:15 PM汇报地点：Room 33 （San Diego Convention Center） 06 摘要号：222 标题：Prospective Study of Avapritinib in Patients with Relapsed/Refractory or MRD-Positive Core-Binding Factor Acute Myeloid Leukemia with KIT Mutations中文标题：阿伐替尼治疗伴KIT突变的复发/难治性或MRD阳性核心结合因子急性髓系白血病患者的前瞻性研究汇报人：Xueqing Dou（苏州大学附属第一医院）汇报时间：Saturday, December 7, 2024: 3:15 PM汇报地点：Seaport Ballroom EFGH （Manchester Grand Hyatt San Diego） 07 摘要号：270 标题：Safety and Efficacy of VA Combined with Modified BuCy Conditioning Regimen Followed By Allo-HSCT for High-Risk or Refractory/Relapsed Acute Lymphoblastic Leukemia : A Prospective, Single-Center, Single-Arm Clinical Trial 中文标题：VA联合改良BuCy预处理方案后行异基因造血干细胞移植治疗高危或难治/复发急性淋巴细胞白血病的安全性和有效性：一项前瞻性、单中心、单臂临床试验汇报人：Xiaoqian Chen（苏州大学附属第一医院）汇报时间：Saturday, December 7, 2024: 3:15 PM 汇报地点：Room 6CF（San Diego Convention Center） 08 摘要号：312 标题：Efficacy and Safety of Adding Blinatumomab to First-Line Treatment for Chinese Children with B-Cell Acute Lymphoblastic Leukemia 中文标题：中国儿童B细胞急性淋巴细胞白血病一线治疗中加用布林妥莫单抗的疗效和安全性汇报人：Ruidong Zhang（首都医科大学附属北京儿童医院血液学中心）汇报时间：Saturday, December 7, 2024: 5:15 PM汇报地点：Marriott Grand Ballroom 5-6 （Marriott Marquis San Diego Marina 09 摘要号：328 标题：Integrative Multi-Omics Analyses Identify a High-Risk Subgroup of Patients with Poor Prognosis in t（8;21） Acute Myeloid Leukemia 中文标题：综合多组学分析鉴定出t（8;21）急性髓系白血病中预后不良的高危亚组汇报人：Yu Liu [中国医学科学院血液病医院（中国医学科学院血液学研究所）]汇报时间：Saturday, December 7, 2024: 4:45 PM汇报地点：Seaport Ballroom ABCD （Manchester Grand Hyatt San Diego） 10 摘要号：345 标题：Mitochondrial Transcriptional-Translational Conflict Contributes to Defective Erythropoiesis and Disease Progression in Splicing Factor Mutant Myelodysplastic Syndromes 中文标题：线粒体转录翻译冲突导致剪接因子突变型骨髓增生异常综合征的红细胞生成缺陷和疾病进展汇报人：Qiaoli Li [中国医学科学院血液病医院（中国医学科学院血液学研究所）]汇报时间：Saturday, December 7, 2024: 4:30 PM汇报地点：Ballroom 20CD （San Diego Convention Center） 11 摘要号：372 标题：Modified Dual CLL1-CD15 and CLL1-CD16 Icar-T Cells for Mitigating Granulocytopenia Toxicities in the Treatment of Acute Myeloid Leukemia 中文标题：改良型双靶点CLL1-CD15和CLL1-CD16 Icar-T细胞用于减轻急性髓系白血病治疗中的粒细胞减少毒性汇报人：Rui Zhang（天津市第一中心医院）汇报时间：Saturday, December 7, 2024: 5:15 PM 汇报地点：Grand Hall C（Manchester Grand Hyatt San Diego） 12 摘要号：452 标题：Spatial Architecture of Immune Microenvironment Orchestrating Anti-Lymphoma Immunity and the Response to Immunochemotherapy in EBV+ Diffused Large B Cell Lymphoma Revealed By Imaging Mass Cytometry and Spatial 中文标题：通过成像质谱流式细胞术和空间转录组揭示EBV+弥漫性大B细胞淋巴瘤中调控抗淋巴瘤免疫和免疫化疗反应的免疫微环境空间结构汇报人：Zhijuan Lin（厦门大学附属第一医院血液科）汇报时间：Sunday, December 8, 2024: 9:45 AM汇报地点：Marriott Grand Ballroom 5-6 （Marriott Marquis San Diego Marina） 13 摘要号：477 标题：Safety and Efficacy of Tgrx-678, a Potent BCR::ABL1 allosteric Inhibitor, in Patients with Tyrosine Kinase Inhibitor Resistant and/or Intolerant Chronic Myeloid Leukemia: Updated Results of Phase 1 Study Tgrx-678 -1001 中文标题：强效BCR::ABL1变构抑制剂Tgrx-678在治疗酪氨酸激酶抑制剂耐药和/或不耐受慢性髓系白血病患者中的安全性和有效性：I期研究Tgrx-678-1001的更新结果汇报人：江倩（北京大学人民医院）汇报时间：Sunday, December 8, 2024: 10:00 AM汇报地点：Harbor Ballroom DEFG （Manchester Grand Hyatt San Diego） 14 摘要号：480 标题：Olverembatinib As Second-Line （2L） Therapy in Patients （pts） with Chronic Phase-Chronic Myeloid Leukemia （CP-CML）中文标题：奥瑞巴替尼作为慢性期慢性髓系白血病（CP-CML）患者二线（2L）治疗药物汇报人：Weiming Li（华中科技大学同济医学院附属协和医院血液科）汇报时间：Sunday, December 8, 2024: 10:45 AM汇报地点：Harbor Ballroom DEFG （Manchester Grand Hyatt San Diego） 15 摘要号：484 标题：Rovadicitinib in Patients with Myelofibrosis Who Were Refractory or Relapsed or Intolerant to Ruxolitinib: A Single Arm, Multicenter, Open-Label, Phase Ib Study 中文标题：Rovadicitinib治疗难治、复发性或对Ruxolitinib不耐受的骨髓纤维化患者：一项单臂、多中心、开放标签、Ib期研究汇报人：常春康（上海交通大学医学院上海第六人民医院血液科）汇报时间：Sunday, December 8, 2024: 10:15 AM汇报地点：Grand Hall C （Manchester Grand Hyatt San Diego） 16 摘要号：486 标题：First-in-Human Phase I/IIa Safety and Efficacy of Flonoltinib Maleate, a New Generation of JAK2/FLT3 Inhibitor in Myelofibrosis 中文标题：新一代JAK2/FLT3抑制剂马来酸氟诺替尼治疗骨髓纤维化的首个人体I/IIa期安全性和有效性研究汇报人：Lijuan Chen（四川大学华西医院血液科）汇报时间：Sunday, December 8, 2024: 10:45 AM汇报地点：Grand Hall C （Manchester Grand Hyatt San Diego） 17 摘要号：576 标题：Clinical Implications of CSF-Ctdna Positivity in Newly Diagnosed Diffuse Large B Cell Lymphoma in a Large Cohort 中文标题：大型队列中新诊断的弥漫性大B细胞淋巴瘤患者脑脊液循环肿瘤DNA（CSF-ctDNA）阳性的临床意义汇报人：梁金花 [南京医科大学第一附属医院（江苏省人民医院）血液科]汇报时间：Sunday, December 8, 2024: 1:15 PM汇报地点：Marriott Grand Ballroom 5-6 （Marriott Marquis San Diego Marina） 18 摘要号：599 标题：Myeloablative Allogeneic Hematopoietic Stem Cell Transplantation Improved Prognosis for Advanced NK/T Cell Lymphoma 中文标题：清髓性异基因造血干细胞移植可改善晚期NK/T细胞淋巴瘤患者的预后汇报人：李智慧（北京高博博仁医院移植科）汇报时间：Sunday, December 8, 2024: 1:00 PM汇报地点：Room 11 （San Diego Convention Center） 19 摘要号：663 标题：Decitabine Plus All-Trans Retinoic Acid Versus Decitabine Monotherapy for Myelodysplastic Syndromes with Excess Blasts: A Multicentre, Randomized Controlled TrialClinically Relevant Abstract 中文标题：地西他滨联合全反式维甲酸对比地西他滨单药治疗伴有过多原始细胞的骨髓增生异常综合征：一项多中心随机对照试验汇报人：佟红艳（浙江大学医学院附属第一医院血液科）汇报时间：Sunday, December 8, 2024: 5:00 PM汇报地点：Harbor Ballroom DEFG （Manchester Grand Hyatt San Diego） 20 摘要号：681 标题：Safety and Efficacy of Bicistronic CD19/CD22 CAR T Cell Therapy in Childhood B Cell Acute Lymphoblastic Leukemia 中文标题：双顺反子CD19/CD22 CAR T细胞疗法在儿童B细胞急性淋巴细胞白血病中的安全性和有效性汇报人：Hua Zhang [SPH生物治疗（上海）有限公司]汇报时间：Sunday, December 8, 2024: 5:00 PM汇报地点：Marriott Grand Ballroom 2-4 （Marriott Marquis San Diego Marina） 21 摘要号：696 标题：Haploidentical Peripheral Blood Stem Cell Combined with Bone Marrow or Unrelated Cord Blood As Grafts for Acute Leukemia/Myelodysplastic Syndrome: An Open-Label, Multicenter, Randomized, Phase 3 Trial 中文标题：单倍体相合外周血干细胞联合骨髓或无关脐带血作为急性白血病/骨髓增生异常综合征移植供体的开放标签、多中心、随机、III期试验汇报人：Sijian Yu（南方医科大学南方医院）汇报时间：Sunday, December 8, 2024: 5:45 PM汇报地点：Room 6A （San Diego Convention Center） 22 摘要号：832 标题：TENT5C As a Target of Chromatin Remodeler SMARCA2 Participates BTK Inhibitor Resistance in Mantle Cell Lymphoma By Regulating ATP Metabolism 中文标题：TENT5C作为染色质重塑剂SMARCA2的靶点，通过调节ATP代谢参与套细胞淋巴瘤对BTK抑制剂的耐药汇报人：Yuting Yan [中国医学科学院血液病医院（中国医学科学院血液学研究所）]汇报时间：Monday, December 9, 2024: 3:30 PM汇报地点：Ballroom 20CD （San Diego Convention Center） 23 摘要号：833 标题：ST6GALNAC4 Promotes Diffuse Large B-Cell Lymphoma Progression Via Mediating Sialylation of Bmpr-1B at Thr24m 中文标题：ST6GALNAC4通过介导BMPR-1B第24位苏氨酸的唾液酸化促进弥漫性大B细胞淋巴瘤进展汇报人：Yu Zhang（山东第一医科大学附属山东省医院血液科）汇报时间：Monday, December 9, 2024: 3:45 PM汇报地点：Ballroom 20CD （San Diego Convention Center） 24 摘要号：836 标题：Venetoclax Combined with Hag Regimen in Newly Diagnosed ETP-ALL: A Prospective, Multicenter, Phase 2 Trial 中文标题：维奈托克联合HAG方案治疗新诊断的早期前体T细胞急性淋巴细胞白血病：一项前瞻性、多中心、II期试验汇报人：Shanshan Suo（浙江大学医学院附属第一医院血液科）汇报时间：Monday, December 9, 2024: 3:00 PM汇报地点：Marriott Grand Ballroom 2-4 （Marriott Marquis San Diego Marina） 25 摘要号：839 标题：Tucidinostat Plus Pediatric-Inspired Chemotherapy As First-Line Therapy for Newly Diagnosed ETP-ALL/Lbl: An Open-Label, Single-Arm, Phase 2 Trial 中文标题：Tucidinostat联合儿童启发化疗作为新诊断的早期前体T细胞急性淋巴细胞白血病/淋巴母细胞淋巴瘤的一线治疗：一项开放标签、单臂、II期试验汇报人：Jieping Lin（南方医科大学南方医院血液科）汇报时间：Monday, December 9, 2024: 3:45 PM汇报地点：Marriott Grand Ballroom 2-4 （Marriott Marquis San Diego Marina） 26 摘要号：843 标题：The Mutated of KRAS gene Determine the Fate of KMT2A-Rearranged AML Patients 中文标题：KRAS基因突变决定KMT2A重排急性髓系白血病患者的命运汇报人：吴一波（浙江大学医学院附属第一医院骨髓移植中心）汇报时间：Monday, December 9, 2024: 3:15 PM汇报地点：Grand Hall C （Manchester Grand Hyatt San Diego） 27 摘要号：874 标题：CD38 Overexpressed Monocytes Play a Critical Role in the Fibrogenesis in Myeloproliferative Neoplasms and Can be Used As a Therapeutic Target to Ameliorate Fibrosis 中文标题：CD38高表达的单核细胞在骨髓增殖性肿瘤纤维化中起关键作用，并可作为改善纤维化的治疗靶点汇报人：Bing Li [中国医学科学院血液病医院（中国医学科学院血液学研究所）]汇报时间：Monday, December 9, 2024: 3:30 PM汇报地点：Seaport Ballroom EFGH （Manchester Grand Hyatt San Diego 28 摘要号：904 标题：CD33 Antibody-Modified Nanoparticles Encapsulated IL-15 Induce ISG15 to Promote MHC I Expression in Leukemia Cells Via Innate Immunity Pathway Inducing Graft-Versus-Leukemia without Aggravating Graft-Versus-Host Disease 中文标题：包裹IL-15的CD33抗体修饰的纳米粒子通过先天免疫途径诱导ISG15促进白血病细胞中MHC I的表达，诱导移植物抗白血病，而不会加重移植物抗宿主病汇报人：Ruowen Wei（华中科技大学同济医学院附属协和医院血液研究所）汇报时间：Monday, December 9, 2024: 3:30 PM汇报地点：Room 6B （San Diego Convention Center） 29 摘要号：921 标题：A Novel Generation of Anti-CD7 Universal CAR-T Therapy for Patients with Relapsed or Refractory CD7 Positive T-ALL/Lbl: A Phase I Clinical Trial 中文标题：新一代抗CD7通用CAR-T疗法治疗复发或难治性CD7阳性T细胞急性淋巴细胞白血病/淋巴母细胞淋巴瘤患者的I期临床试验汇报人：胡永仙（浙江大学医学中心良渚实验室）汇报时间：Monday, December 9, 2024: 3:15 PM汇报地点：Hall B （San Diego Convention Center） 30 摘要号：923 标题：A Prospective Investigator-Initiated Phase 1/2 Study of BCMA/CD19 Dual-Targeting CAR T Therapy in Patients with Relapsed/Refractory Multiple Myeloma Including Those with Extramedullary Disease 中文标题：一项前瞻性研究者发起的BCMA/CD19双靶点CAR T细胞疗法治疗复发/难治性多发性骨髓瘤（包括髓外病变患者）的I/II期研究汇报人：Hua Jiang（同济大学医学院上海第四人民医院）汇报时间：Monday, December 9, 2024: 3:45 PM汇报地点：Hall B （San Diego Convention Center） 31 摘要号：956 标题：A Highly Selective and Orally Bioavailable CK1α Molecular Glue Degrader Targets B-Cell Lymphoma Cells 中文标题：一种高选择性和口服生物可利用的CK1α分子胶降解剂靶向B细胞淋巴瘤细胞汇报人：Ran Kong（山东大学山东省医院血液科）汇报时间：Monday, December 9, 2024: 4:45 PM汇报地点：Ballroom 20CD （San Diego Convention Center） 32 摘要号：958 标题：KPT-330 Combined with Radiation Therapy: Effective Central Nervous System Lymphoma Treatment with Reduced Neurotoxicity 中文标题：KPT-330联合放疗有效治疗中枢神经系统淋巴瘤并降低神经毒性汇报人：Bingzong Li（苏州大学附属第二医院）汇报时间：Monday, December 9, 2024: 5:15 PM汇报地点：Ballroom 20CD （San Diego Convention Center） 33 摘要号：960 标题：CD93+ Myeloid Cells Suppress T-Cell-Mediated Anti-Tumor Immunity 中文标题：CD93+髓系细胞抑制T细胞介导的抗肿瘤免疫汇报人：Hui Yu（北京大学肿瘤医院）汇报时间：Monday, December 9, 2024: 5:45 PM汇报地点：Ballroom 20CD （San Diego Convention Center） 34 摘要号：964 标题：CD7 CAR T-Cell Therapy in Relapsed or Refractory T-Cell Acute Lymphoblastic Leukemia: A Retrospective Study 中文标题：CD7 CAR-T细胞疗法治疗复发或难治性T细胞急性淋巴细胞白血病的回顾性研究汇报人：潘静（北京高博医院）汇报时间：Monday, December 9, 2024: 5:15 PM汇报地点：Marriott Grand Ballroom 5-6 （Marriott Marquis San Diego Marina） 35 摘要号：971 标题：Venetoclax and Decitabine Compared with Standard Intensive Chemotherapy As Induction Therapy in Newly Diagnosed Acute Myeloid Leukemia: Updated Results of a Multicenter, Randomized, Phase 2b Trial 中文标题：维奈托克联合地西他滨与标准强化化疗作为新诊断急性髓系白血病诱导治疗的比较：一项多中心、随机、IIb期试验的更新结果汇报人：Jing Lu（苏州大学附属第一医院）汇报时间：Monday, December 9, 2024: 5:30 PM汇报地点：Grand Hall B （Manchester Grand Hyatt San Diego） 36 摘要号：972 标题：High-Dose Cytarabine with Idarubicin Versus High-Dose Cytarabine within First Consolidation for Acute Myeloid Leukemia in First Complete Remission: An Open-Label, Multicenter, Randomized, Phase 3 Trial 中文标题：首次完全缓解期急性髓系白血病患者首次巩固治疗中高剂量阿糖胞苷联合伊达比星对比高剂量阿糖胞苷：一项开放标签、多中心、随机、III期试验汇报人：Zinan Feng（南方医科大学南方医院血液科）汇报时间：Monday, December 9, 2024: 5:45 PM汇报地点：Grand Hall B （Manchester Grand Hyatt San Diego） 37 摘要号：977 标题：Faecalibacterium Prausnitzii Confers a Protective Effect Against the Development of NKTCL 中文标题：Prausnitzii粪杆菌对NKTCL的发展具有保护作用汇报人：Zhuangzhuang Shi（郑州大学第一附属医院）汇报时间：Monday, December 9, 2024: 5:30 PM汇报地点：Marriott Grand Ballroom 11-13 （Marriott Marquis San Diego Marina） 38 摘要号：986 标题：Final Analysis of a Phase 1 Study of Zanubrutinib Plus Lenalidomide in Patients With Relapsed/Refractory Diffuse Large B-cell Lymphoma 中文标题：泽布替尼联合来那度胺治疗复发/难治性弥漫大 B 细胞淋巴瘤患者的I期临床研究最终分析汇报人：宋拯（天津医科大学肿瘤医院）汇报时间：Monday, December 9, 2024: 4:45 PM汇报地点：Pacific Ballroom Salons 18-19 （Marriott Marquis San Diego Marina） 39 摘要号：1002 标题：The Efficacy and Safety of Selinexor in Combination with Ruxolitinib in Ruxolitinib-Treated Myelofibrosis Patients: The Interim Analysis of a Prospective, Open-Label, Multicenter, Parallel-Cohort, Phase 2 Study 中文标题：塞利尼索联合芦可替尼治疗经芦可替尼治疗的骨髓纤维化患者的疗效和安全性：一项前瞻性、开放标签、多中心、平行队列、II期研究的期中分析汇报人：段明辉 [中国医学科学院北京协和医院（北京协和医院）]汇报时间：Monday, December 9, 2024: 5:45 PM汇报地点：Harbor Ballroom DEFG （Manchester Grand Hyatt San Diego） 40 摘要号：1028 标题：A Single-Center, Single-Arm, Phase I Clinical Trial of Anti-BCMA/GPRC5D Bispecific CAR T-Cells in Patients with Refractory and Relapsed Multiple Myeloma with Extramedullary Disease 中文标题：一项单中心、单臂、I期临床试验：抗BCMA/GPRC5D双特异性CAR-T细胞治疗伴有髓外病变的复发/难治性多发性骨髓瘤患者汇报人：Ling Qiu（中国人民解放军西部战区总医院血液科）汇报时间：Monday, December 9, 2024: 4:45 PM汇报地点：Pacific Ballroom Salons 24-26 （Marriott Marquis San Diego Marina） 41 摘要号：1049 标题：Mini-Dosed Blinatumomab Maintenance Therapy Following Allogeneic Hematopoietic Stem Cell Transplantation in Acute B-Cell Lymphoblastic Leukemia 中文标题：异基因造血干细胞移植后微小剂量Blinatumomab维持治疗急性B细胞淋巴细胞白血病汇报人：Jie Ji（四川大学华西医院）汇报时间：Monday, December 9, 2024: 5:30 PM汇报地点：Room 6A （San Diego Convention Center） 42 摘要号：1050 标题：Updated Results from a Phase II Clinical Trial Safety and Efficacy of Azacitidine and Chidamide Maintenance after Allogeneic Hematopoietic Stem Cell Transplantation for Patients with High-Risk Acute Myeloid Leukemia 中文标题：高危急性髓系白血病患者异基因造血干细胞移植后地西他滨和西达本胺维持治疗的II期临床试验安全性和有效性的更新结果汇报人：Rui Huang（南方医科大学珠江医院）汇报时间：Monday, December 9, 2024: 5:45 PM汇报地点：Room 6A （San Diego Convention Center）非恶性血液疾病篇 PART.02 01 摘要号：12 标题：Rbm38 Regulates Heme Biosynthesis Via Fine-Tuning the RNA Alternative Splicing, Stability and Translation of Porphyrin Metabolic Enzyme Gene Ferrochelatase （Fech）中文标题：Rbm38通过精细调节卟啉代谢酶基因铁螯合酶（Fech）的RNA可变剪接、稳定性和翻译来调控血红素生物合成汇报人：Yang Mei（湖南大学附属湘潭中心医院）汇报时间：Saturday, December 7, 2024: 10:45 AM汇报地点：Room 29 （San Diego Convention Center） 02 摘要号：30 标题：Clec16a-Mediated Mitophagy Modulates Zebrafish Definitive Hematopoiesis 中文标题：Clec16a介导的线粒体自噬调节斑马鱼确定性造血汇报人：Shuyang Cai（上海中医药大学上海市中医医院）汇报时间：Saturday, December 7, 2024: 10:45 AM汇报地点：Room 6DE （San Diego Convention Center） 03 摘要号：97 标题：JAK/Rock Inhibitor Rovadicitinib for Glucocorticoid-Refractory or -Dependent Chronic Graft-Versus-Host Disease updated Results of Multicenter, Phase 1b/2a Trial 中文标题：JAK/ROCK抑制剂Rovadicitinib治疗糖皮质激素难治性或依赖性慢性移植物抗宿主病：多中心Ⅰb/Ⅱa期试验的最新结果汇报人：赵妍敏（浙江大学医学院附属第一医院骨髓移植中心）汇报时间：Saturday, December 7, 2024: 9:30 AM汇报地点：Ballroom 20CD （San Diego Convention Center） 04 摘要号：99 标题：A Phase II Study to Evaluate the Efficacy and Safety of Pimicotinib （ABSK021） in Chronic Graft Versus Host Disease （cGvHD） after 1 or More Lines of Systemic Treatment 中文标题：一项评估匹米替尼（ABSK021）在经1种或多种全身治疗后的慢性移植物抗宿主病（cGvHD）中疗效和安全性的II期研究汇报人：吴德沛（苏州大学附属第一医院）汇报时间：Saturday, December 7, 2024: 10:00 AM汇报地点：Ballroom 20CD （San Diego Convention Center） 05 摘要号：101 标题：Multiomic Analyses Uncover Immune Signatures of Steroid-Refractory Graft-Versus-Host Disease 中文标题：多组学分析揭示类固醇难治性移植物抗宿主病的免疫特征汇报人：Zengkai Pan（上海交通大学医学院附属瑞金医院）汇报时间：Saturday, December 7, 2024: 10:30 AM汇报地点：Ballroom 20CD （San Diego Convention Center） 06 摘要号：125 标题：Imbalanced Expression of TACI Isoforms Regulated By TNFRSF13B Variants Promotes the Progression of Epstein-Barr Virus-Associated Lymphoproliferative Diseases 中文标题：由TNFRSF13B变异调控的TACI异构体表达失衡促进EB病毒相关淋巴增殖性疾病的进展汇报人：Xinyue Deng（华中科技大学同济医学院附属同济医院）汇报时间：Saturday, December 7, 2024: 1:00 PM汇报地点：Room 11 （San Diego Convention Center） 07 摘要号：150 标题：Efficient Generation of CAR-T By the First Coacervate-Based Gene Delivery System 中文标题：基于首个共聚体基因递送系统高效生成CAR-T细胞汇报人：Peipei Zhu（西湖大学）汇报时间：Saturday, December 7, 2024: 1:15 PM汇报地点：Room 25 （San Diego Convention Center） 08 摘要号：164 标题：Reconstruction of Megaloblastic Anemia in a Novel Erythroblastic Island Humanized Mouse Model with Mature Circulating Human Red Blood Cells 中文标题：在具有成熟循环人红细胞的新型红系造血岛人源化小鼠模型中重建巨幼细胞性贫血汇报人：Shuang Liu（南京大学医学院模型动物研究中心）汇报时间：Saturday, December 7, 2024: 2:15 PM汇报地点：Room 33 （San Diego Convention Center） 09 摘要号：192 标题：Exploring the Mechanism of Chromatin Spatial Structure Changes and Transcriptional Regulation in Age-Related Clonal Hematopoiesis Caused By DNMT3A Mutations Using Chromatin Capture Technology 中文标题：利用染色质捕获技术探索由DNMT3A突变引起的与年龄相关的克隆性造血中染色质空间结构变化及转录调控机制汇报人：Yujun Dai（中山大学肿瘤防治中心）汇报时间：Saturday, December 7, 2024: 3:15 PM 汇报地点：Grand Hall D (Manchester Grand Hyatt San Diego) 10 摘要号：263 标题：Targeting the Hypoxic Microenvironment in Cutaneous Chronic Graft-Versus-Host Disease through PI3K Inhibition 中文标题：通过PI3K抑制靶向皮肤慢性移植物抗宿主病的缺氧微环境汇报人：Yuxi Xu（陆军军医大学新桥医院血液病医学中心）汇报时间：Saturday, December 7, 2024: 3:00 PM汇报地点：Room 6B （San Diego Convention Center） 11 摘要号：266 标题：Elevated Dosing of Recombinant Human Thrombopoietin Accelerates Platelet Engraftment in Allogeneic Hematopoietic Stem Cell Transplantation: A Prospective, Dosage-Optimization, Controlled Clinical Study 中文标题：增加重组人血小板生成素剂量可加速异基因造血干细胞移植后血小板植入：一项前瞻性、剂量优化、对照临床研究汇报人：Dan Feng [中国医学科学院血液病医院（中国医学科学院血液学研究所）]汇报时间：Saturday, December 7, 2024: 2:15 PM汇报地点：Room 6CF （San Diego Convention Center） 12 摘要号：268 标题：Epstein-Barr Virus Reactivation and Post-Transplant Lymphoproliferative Disorders after Allo-HSCT in the Era of Letermovir for Cytomegalovirus Prophylaxis 中文标题：在利特莫韦预防巨细胞病毒感染时代异基因造血干细胞移植后EB病毒再激活和移植后淋巴增殖性疾病汇报人：Jingtao Huang（上海血液学研究所）汇报时间：Saturday, December 7, 2024: 2:45 PM汇报地点：Room 6CF （San Diego Convention Center） 13 摘要号：300 标题：Effects of Low-Molecular-Weight Heparin on Pregnancy Outcomes in Protein S Deficiency: A Prospective, Randomized Controlled Phase II Clinical 中文标题：低分子肝素对蛋白S缺乏症患者妊娠结局的影响：一项前瞻性、随机对照II期临床研究汇报人：Mengtong Zang（北京大学人民医院）汇报时间：Saturday, December 7, 2024: 5:15 PM汇报地点：Room 29 （San Diego Convention Center） 14 摘要号：304 标题：Hetrombopag Added to Immunosuppressive Therapy in First-Line Treatment of Severe Aplastic Anemia: A Randomized, Double-Blind, Placebo-Controlled Phase 3 Trial 中文标题：一线治疗重型再生障碍性贫血时，在免疫抑制疗法中添加海曲泊帕：一项随机、双盲、安慰剂对照的III期试验汇报人：张凤奎 [中国医学科学院血液病医院（中国医学科学院血液学研究所）] 汇报时间：Saturday, December 7, 2024: 4:45 PM 汇报地点：Room 11 （San Diego Convention Center） 15 摘要号：378 标题：A Multi-Center Clinical Trial of Allogeneic Hematopoietic Stem Cell Transplants in Transfusion Dependent Thalassemia 中文标题：输血依赖性地中海贫血患者异基因造血干细胞移植的多中心临床试验汇报人：Rongrong Liu（广西医科大学附属第一医院血液科）汇报时间：Saturday, December 7, 2024: 5:15 PM汇报地点：Room 6DE （San Diego Convention Center） 16 摘要号：420 标题：A Single-Cell Transcriptomic Atlas of Cytokine Storm in CAR-T Therapy, COVID-19, and SLE 中文标题：CAR-T疗法、COVID-19和系统性红斑狼疮中细胞因子风暴的单细胞转录组图谱汇报人：Xia Li（浙江大学医学院附属第一医院骨髓移植中心）汇报时间：Sunday, December 8, 2024: 10:45 AM汇报地点：Grand Hall D （Manchester Grand Hyatt San Diego） 17 摘要号：425 标题：β2-Adrenergic Receptor Agonist Terbutaline Regulates Macrophage Polarization Via HMGB1 in Immune Thrombocytopenia 中文标题：β2-肾上腺素受体激动剂特布他林通过HMGB1调节免疫性血小板减少症中的巨噬细胞极化汇报人：Qiuyu Guo（北京大学人民医院）汇报时间：Sunday, December 8, 2024: 10:30 AM汇报地点：Room 28 A-D （San Diego Convention Center） 18 摘要号：426 标题：Differentiation Route Generates Functional Biased Platelets and Responses Distinctly to Varying Physiological Demands 中文标题：分化途径产生功能偏倚的血小板，并对不同的生理需求产生不同的反应汇报人：Jingkun Liu（中国国家生物信息中心）汇报时间：Sunday, December 8, 2024: 10:45 AM汇报地点：Room 28 A-D （San Diego Convention Center） 19 摘要号：437 标题：ERAD Activity Distinguishes the Functional Heterogeneity of Hematopoietic Stem Cells 中文标题：ERAD活性区分造血干细胞的功能异质性汇报人：QinLu Peng（湖南省动物模型与分子医学重点实验室）汇报时间：Sunday, December 8, 2024: 10:30 AM汇报地点：Room 7 （San Diego Convention Center） 20 摘要号：438 标题：SNORD113-114 Cluster Maintains Hematopoietic Stem Cell Self-Renewal Via Orchestrating the Translation Machinery 中文标题：SNORD113-114基因簇通过协调翻译机制维持造血干细胞自我更新汇报人：Hui Wang（浙江大学医学院附属第一医院骨髓移植中心）汇报时间：Sunday, December 8, 2024: 10:45 AM汇报地点：Room 7 （San Diego Convention Center） 21 摘要号：538 标题：Polycomb Repressive Complex 2 Regulates Differentiation-Stage-Specific Autophagy Gene Expression and Safeguards Normal Erythropoiesis 中文标题：多梳抑制复合体2调控分化阶段特异性的自噬基因表达并保障正常红细胞生成汇报人：Jiazhuo Li（华南理工大学医学院附属第二医院）汇报时间：Sunday, December 8, 2024: 12:45 PM汇报地点：Room 6DE （San Diego Convention Center） 22 摘要号：539 标题：A Novel Role of LKB1 in Erythroblast Enucleation 中文标题：LKB1在红系细胞脱核中的新作用汇报人：Yuanlin Xu [河南省肿瘤医院（郑州大学附属肿瘤医院）] 汇报时间：Sunday, December 8, 2024: 1:00 PM汇报地点：Room 6DE （San Diego Convention Center） 23 摘要号：562 标题：Procr+ Endothelial Progenitor Cells Modulate Adult Hematopoiesis and Microenvironment Homeostasis Via Notch Signaling 中文标题：Procr+内皮祖细胞通过Notch信号通路调节成人造血和微环境稳态汇报人：Chang Xu [中国医学科学院血液病医院（中国医学科学院血液学研究所）]汇报时间：Sunday, December 8, 2024: 12:45 PM汇报地点：Room 7 （San Diego Convention Center） 24 摘要号：682 标题：CD19 CAR T-Cell Therapy in Refractory Autoimmune Hemolytic Anemia 中文标题：CD19 CAR T细胞疗法治疗难治性自身免疫性溶血性贫血汇报人：Ruonan Li[中国医学科学院血液病医院（中国医学科学院血液学研究所）]汇报时间：Sunday, December 8, 2024: 5:15 PM汇报地点：Marriott Grand Ballroom 2-4 （Marriott Marquis San Diego Marina） 25 摘要号：683 标题：Sequential Infusion of Anti-CD19 and Anti-BCMA Chimeric Antigen Receptor T-Cells: A Promising Treatment Strategy for Refractory Immune-Mediated Platelet Transfusion Refractoriness 中文标题：序贯输注抗CD19和抗BCMA嵌合抗原受体T细胞：一种治疗难治性免疫介导的血小板输注无效的有前景的治疗策略汇报人：Yunju Ma（苏州大学附属第一医院）汇报时间：Sunday, December 8, 2024: 5:30 PM汇报地点：Marriott Grand Ballroom 2-4 （Marriott Marquis San Diego Marina） 26 摘要号：690 标题：Parvovirus B19 Originates from Infected Hematopoietic Stem Cells Following Hematopoietic Stem Cell Transplantation 中文标题：细小病毒B19起源于造血干细胞移植后受感染的造血干细胞汇报人：Xuying Pei（北京大学人民医院）汇报时间：Sunday, December 8, 2024: 5:45 PM汇报地点：Room 6B （San Diego Convention Center） 27 摘要号：711 标题：Preliminary Efficacy and Safety Results of TQB3473, a Novel Syk Inhibitor, in Adult Patients with Immune Thrombocytopenia （ITP）中文标题：新型Syk抑制剂TQB3473治疗成人免疫性血小板减少症（ITP）的初步疗效和安全性结果汇报人：周虎 [河南省肿瘤医院（郑州大学附属肿瘤医院）]汇报时间：Monday, December 9, 2024: 11:00 AM汇报地点：Room 29 （San Diego Convention Center） 28 摘要号：712 标题：Updated Outcome from Biomarker MSC-C5b-9-Guided All-Trans Retinoic Acid Treatment for Resistant/Recurrent ITP: A Multicenter, Randomized, Open-Label, Phase 3 Clinical Trial 中文标题：生物标志物MSC-C5b-9指导的全反式维甲酸治疗难治/复发免疫性血小板减少症（ITP）的最新疗效：一项多中心、随机、开放标签、III期临床试验汇报人：Menglin Li（北京大学人民医院）汇报时间：Monday, December 9, 2024: 11:15 AM汇报地点：Room 29 （San Diego Convention Center） 29 摘要号：806 标题：Rovadicitinib in Patients with Hemophagocytic Lymphohistiocytosis: A Single Arm, Open-Label, Phase I Study 中文标题：Rovadicitinib治疗噬血细胞性淋巴组织细胞增生症患者的单臂、开放标签、I期研究汇报人：王昭（北京友谊医院）汇报时间：Monday, December 9, 2024: 3:00 PM 汇报地点：Room 6DE （San Diego Convention Center） 30 摘要号：810 标题：Pharmacological and Mechanism Study of a New RIPK1 Inhibitor Via Necroptosis to Treat Hemophagocytic Lymphohistiocytosis 中文标题：一种新型RIPK1抑制剂通过坏死性凋亡治疗噬血细胞性淋巴组织细胞增生症的药理学及机制研究汇报人：Jinbing Zhu（四川大学华西医院）汇报时间：Monday, December 9, 2024: 4:00 PM汇报地点：Room 6DE （San Diego Convention Center） 31 摘要号：893 标题：Venetoclax Plus Dexamethasone As First-Line Treatment for t（11; 14） Light-Chain Amyloidosis: Preliminary Result of a Phase II Prospective, Multicenter, Single-Arm Study 中文标题：维奈托克联合地塞米松作为t（11;14）轻链淀粉样变性的一线治疗：一项II期前瞻性、多中心、单臂研究的初步结果汇报人：Kaini Shen [中国医学科学院北京协和医院（北京协和医院）]汇报时间：Monday, December 9, 2024: 3:45 PM汇报地点：Seaport Ballroom EFGH （Manchester Grand Hyatt San Diego） 32 摘要号：1044 标题：A Multicenter Randomized Controlled Trial of Low-Dose Ruxolitinib for Gvhd Prophylaxis in Haploidentical Hematopoietic Stem Cell Transplantation 中文标题：低剂量芦可替尼在同种异基因造血干细胞移植中预防移植物抗宿主病的多中心随机对照试验汇报人：Hengwei Wu（浙江大学医学院附属第一医院骨髓移植中心）汇报时间：Monday, December 9, 2024: 5:45 PM汇报地点：Room 6B （San Diego Convention Center）（来源：《肿瘤瞭望–血液时讯》编辑部）声明凡署名原创的文章版权属《肿瘤瞭望》所有，欢迎分享、转载。本文仅供医疗卫生专业人士了解最新医药资讯参考使用，不代表本平台观点。该等信息不能以任何方式取代专业的医疗指导，也不应被视为诊疗建议，如果该信息被用于资讯以外的目的，本站及作者不承担相关责任。

细胞疗法免疫疗法临床研究ASH会议

2024-06-03

·BioSpace

Hemostemix Announces Strategic Manufacturing Partnership with CytoImmune Therapeutics and $1,800,000 in Financing Commitments

Calgary, Alberta--(News - June 3, 2024) - Hemostemix Inc. (TSXV: HEM) (OTC Pink: HMTXF) (FSE: 2VF0) is pleased to announce it has signed a Letter of Intent ("LOI") with CytoImmune Therapuetics ("CytoImmune") to re-establish production of ACP-01 ("ACP") in CytoImmune's state-of-the-art clinical cell manufacturing facility. The Company is also pleased to announce that it has received commitments for $1,800,000 of Units in a non-brokered private placement as more fully described below. CytoImmune To view an enhanced version of this graphic, please visit: CytoImmune has approximately 40 employees with hundreds of years of cumulative experience in biologics and cell manufanufacturing along with a 38,000 square foot state-of-the-art cell manufacturing facility in Toa Baja, Puerto Rico. CytoImmune is entering a technology transfer and manufacturing agreement with Hemostemix for the commercial supply of ACP-01. In addition, CytoImmune will subscribe for $1,370,000 of Units of Hemostemix at $0.05 as described below. This commitment underscores CytoImmune's dedication to fostering partnerships that fuel the future of cell therapy and improve patients' lives. "Our company's industry-leading expertise in cell therapy development and clinical manufacturing will accelerate Hemostemix's success and expand Puerto Rico's legacy as "America's Medicine Cabinet," said Jose Vidal, CEO of CytoImmune Therapeutics, Inc. "Puerto Rico employs nearly 100,000 pharmaceutical executives and manufactures nearly 20% of the United States drug exports. Adding cell and gene therapies is driven by Puerto Rico's initiative to rejuvenate its biopharma sector with new technologies." Globally, 236 million suffer from Peripheral Arterial Disease. Approximately 10% of these patients degenerate into CLTI. The incidence of CLTI in the U.S.A. is 1.33%, with an annual 10-40% amputation rate, and an annual 15-20% mortality rate. Globally, CLTI has a 60% mortality rate in 5 years. Therefore, saving a limb is saving a life. In Hemostemix's phase II clinical trial of ACP-01, 83% of patients followed for up to 4.5 years by the University of Toronto and University of British Columbia experienced healing of ulcers, cessation of pain, no major amputation, and improved. Unblinded, these 83% were treated with ACP. "This is a pivotal agreement that re-establishes production of ACP for sale to patients suffering from no-option chronic limb threatening ischemia and heart disease, under physician order," stated Thomas Smeenk, CEO. "It enables Hemostemix to ramp up production with CytoImmune, and with its own staff, to reach sales volumes of up to $2 million per month in 2025," Smeenk said. Hemostemix has organized with the principal investigators of its phase II trial up to 226 patients/month of CLTI specialist capacity. Globally, this provides individuals who are suffering in significant pain and facing limb amputation a second-opinion-before-amputation. Likewise, Hemostemix has organized with invasive cardiologists who completed 200 regulatory approved ACP heart treatments, capacity to treat 100 heart patients per month. Non-Brokered Private Placement (the "Offering") The Company may raise up to $2,000,000, or more if oversubscribed, from the sale of Units. Each Unit at $0.05 shall consist of one common share in the capital of the Company ("Common Share") and one common share purchase warrant ("Warrant"), with each Warrant entitling the holder to acquire one Common Share at a price of $0.12 per Common Share for a period of 24 months from the closing of the Offering, subject to the accelerated expiry provision described below. If during any 10 consecutive trading days occurring after four months and one day has elapsed following the closing date of the Offering, the weighted average closing sales price of the Common Shares (or the closing bid, if no sales were reported on a trading day) as quoted on the TSX Venture Exchange ("Exchange") is greater than or equal to $0.15 per Common Share, the Company may provide notice in writing to the holders of the Warrants by issuance of a press release that the expiry date of the Warrants will be accelerated to the 30th day after the date on which the Company issues such press release. As announced on March 7th, 2024, the Company is continuing to work with Oak Hill Asset Management to raise low-dilution capital and to accelerate its business plan of offering no-option CLTI patients an outpatient procedure to save their limb from amputation under physician order. Proceeds from the Offering and other funding initiatives, will be used to initiate the processing of initial batches in 2024 and for general working capital purposes. Certain directors of the Company may participate in the private placement, which would constitute a "related party transaction" within the meaning of Multilateral Instrument 61-101 - Protection of Minority Security Holders in Special Transactions ("MI 61-101") and the policies of the TSXV. The Company is relying upon the exemptions from the formal valuation and minority shareholder approval requirements pursuant to sections 5.5(b) and 5.7(1)(a), respectively, of MI 61-101 on the basis that the Company is not listed on a specified stock exchange and, at the time the Offering was agreed to, neither the fair market value of the subject matter of, nor the fair market value of the consideration for, the transaction insofar as it involves an interested party (within the meaning of MI 61-101) in the Offering, exceeds 25% of the Company's market capitalization calculated in accordance with MI 61-101. All securities issued under the Private Placement will be subject to a four-month hold period from the closing date under applicable Canadian securities laws, in addition to such other restrictions as may apply. About CytoImmune Therapeutics CytoImmune Therapeutics is at the forefront of a novel natural killer cell therapy for lung cancer, currently in phase 1 clinical trials. In addition, we are now offering cell therapy development and clinical manufacturing services to both biotechnology companies and academia. Our state-of-the-art clinical cell manufacturing facility in Toa Baja, Puerto Rico, is custom built to support the development and commercialization of cutting-edge T cell or NK cell therapies. At CytoImmune, we are dedicated to fostering collaborations that drive the future of cell therapy and improve the lives of cancer patients. Discover how our expertise in cell therapy development and clinical manufacturing can accelerate your path to success. For additional information, please visit: Cytoimmune.com. About Hemostemix Hemostemix is an autologous stem cell therapy company, founded in 2003. A winner of the World Economic Forum Technology Pioneer Award, the Company has developed, patented, and is scaling a patient's blood-based stem cell therapeutics platform that includes angiogenic cell precursors, neuronal cell precursor and cardiomyocyte cell precursors. For more information, please visit Hemostemix.com. For further information, please contact: Thomas Smeenk, President, CEO & Co-Founder EM: tsmeenk@hemostemix.com PH: 905-580-4170 Neither the TSX Venture Exchange nor its Regulation Service Provider (as that term is defined under the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release. Forward-Looking Information: This news release contains "forward-looking information" within the meaning of applicable Canadian securities legislation. All statements, other than statements of historical fact, included herein are forward-looking information. In particular, this news release contains forward-looking information in relation to: financing of the Company and its lead product ACP-01, and the commercialization of ACP-01 via the sale of compassionate treatments under physician order. ‎There can be no assurance that such forward-looking information will prove to be accurate. Actual results and future events could differ materially from those anticipated in such forward-looking information. This forward-looking information reflects Hemostemix's current beliefs and is based on information currently available to Hemostemix and on assumptions Hemostemix believes are reasonable. These assumptions include, but are not limited to: the underlying value of Hemostemix and its Common Shares; the successful resolution of the litigation that Hemostemix is pursuing or defending (the "Litigation"); the results of ACP-01 research, trials, studies and analyses, including the analysis being equivalent to or better than previous research, trials or studies; the receipt of all required regulatory ‎approvals for research, trials or studies; the level of activity, market acceptance and market trends in the healthcare sector; the ‎economy generally; consumer ‎interest in Hemostemix's services and products; competition and ‎Hemostemix's competitive advantages; and Hemostemix obtaining satisfactory financing to ‎ fund Hemostemix's operations including any research, trials or studies, and any Litigation. Forward-looking information is Subject to known and unknown risks, uncertainties and other factors that may cause the actual results, level of activity, performance or achievements of Hemostemix to be materially different from those expressed or implied by such forward-looking information. Such risks and other factors may include, but are not limited to: the ability of Hemostemix to complete clinical trials, complete a satisfactory analyses and results of such analyses to gain regulatory approval of a phase II or phase III clinical trial of ACP-01; potential litigation Hemostemis mayface; general business, economic, competitive, political and social uncertainties; general capital market conditions and market prices for securities; delay or failure to receive board or regulatory approvals; the actual results of future operations including the actual results of future research, trials or studies; competition; changes in legislation ‎affecting Hemostemix; the timing and availability of external financing on acceptable terms; long-term capital requirements and future developments in Hemostemix's markets and the markets in which it expects to compete;‎ lack of qualified, skilled labour or loss of key individuals; and risks ‎related to the COVID-19 pandemic including various recommendations, orders and measures of governmental authorities to ‎try to limit the pandemic, including travel restrictions, border closures, non-essential business closures service disruptions, quarantines, self-isolations, shelters-in-place and social distancing, disruptions to markets, disruptions to economic activity and ‎financings, disruptions to supply chains and sales channels, and a deterioration of general economic conditions including a ‎possible national or global recession or depression; the potential impact that the COVID-19 pandemic may have on Hemostemix which may include a decreased demand for the services that Hemostemix offers; and a deterioration of financial markets that could limit Hemostemix's ability to obtain external financing. A description of additional risk factors that may cause actual results to differ materially from forward-looking information can be found in Hemostemix's disclosure documents on the SEDAR website at . Although Hemostemix has attempted to identify important factors that could cause actual results to differ materially from those contained in forward-looking information, there may be other factors that cause results not to be as anticipated, estimated or intended. Readers are cautioned that the foregoing list of factors is not exhaustive. Readers are further cautioned not to place undue reliance on forward-looking information as there can be no assurance that the plans, intentions or expectations upon which they are placed will occur. Forward-looking information contained in this news release is expressly qualified by this cautionary statement. The forward-looking information contained in this news release represents the expectations of Hemostemix as of the date of this news release and, accordingly, it is Subject to change after such date. However, Hemostemix expressly disclaims any intention or obligation to update or revise any forward-looking information, whether as a result of new information, future events or otherwise, except as expressly required by applicable securities law. To view the source version of this press release, please visit

细胞疗法临床2期临床1期

2024-03-08

·BioSpace

Hemostemix Announces Engagement of Oak Hill Asset Management Inc.

Calgary, Alberta--(News - March 7, 2024) - Hemostemix Inc. (TSXV: HEM) (OTCQB: HMTXF) (FSE: 2VF0) ("Hemostemix" or the "Company") is pleased to announce the non-exclusive engagement of Oak Hill Asset Management Inc. ("OHAM"), an Exempt Market Dealer to provide capital markets advice related to the Company's capital markets strategy. Services include advice on the structure of equity or debt capital financing and the identification of potential future investors. The Company intends to raise approximately C$6 million in low-dilution capital (the "Offering"). Proceeds will be used to re-establish production of ACP-01 for sale as an exempt compassionate treatment and to complete its phase III CLTI clinical trial. Pursuant to an engagement letter between the Company and OHAM, the Company has agreed to pay OHAM a cash fee of $12,000 plus $20,000 in common shares as a work fee. Additional fees would be paid on any financing raised by OHAM. Proceeds from the Offering will allow the Company to lease ready-to-occupy cGMP production capacity in Puerto Rico in 2024 and generate revenue by the end of 2025 through 30-40 exempt compassionate treatments per month, while scaling production and progressing its clinical trial. Sales of ACP for CLTI treatments will be through clinical trial sites (to patients who do not meet inclusion criteria), through limb salvage clinics and podiatrists. To-date, seven clinical trial sites have agreed to refer patients to Hemostemix for exempt compassionate treatments; and, have agreed to process up to 226 of Hemostemix's referrals to them per month. Puerto Rico's Act 60 legislation enables the company to obtain 50% cash back on eligible expenses including clinical trials. Additionally, ACT 60 provides the company with a 15-year 1% profit tax structure, and a 20% tax credit for offshore expenses. The structure and price of the Offering has yet to be determined and the Company will issue a follow-up news release once details are available. The Company is confident that it can be completed on a low-dilutive basis that appropriately values the significant, near-term revenue and cash flow streams. "The 498 treatments of ACP, including the seven clinical studies published in peer reviewed journals to-date, demonstrate ACP is safe and effective in the treatment of peripheral arterial disease and three forms of heart disease," stated Thomas Smeenk, CEO. "It is remarkable that the clinical trial sites will be able to refer and see up to 226 no-option referrals. Compared to no-option and amputation, an ACP injection under exemption to save the limb makes sense," Smeenk said. ABOUT HEMOSTEMIX Hemostemix is an autologous stem cell therapy company, founded in 2003. A winner of the World Economic Forum Technology Pioneer Award, the Company has developed, patented, and is scaling a patient's blood-based stem cell therapeutics platform that includes angiogenic cell precursors, neuronal cell precursor and cardiomyocyte cell precursors. For more information, please visit For further information, please contact: Thomas Smeenk, President, CEO & Co-Founder EM: tsmeenk@hemostemix.com PH: 905-580-4170 Neither the TSX Venture Exchange nor its Regulation Service Provider (as that term is defined under the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release. Forward-Looking Information: This news release contains "forward-looking information" within the meaning of applicable Canadian securities legislation. All statements, other than statements of historical fact, included herein are forward-looking information. In particular, this news release contains forward-looking information in relation to: the engagement of Oak Hill Financial, the sales of ACP-01 as an exempt compassionate treatment, the licensing of ACP-01, the Trademark Know Your Health! and related results, including the commercialization of ACP-01. ‎‎There can be no assurance that such forward-looking information will prove to be accurate. Actual results and future events could differ materially from those anticipated in such forward-looking information. This forward-looking information reflects Hemostemix's current beliefs and is based on information currently available to Hemostemix and on assumptions Hemostemix believes are reasonable. These assumptions include, but are not limited to: the underlying value of Hemostemix and its Common Shares; the successful resolution of the litigation that Hemostemix is pursuing or defending (the "Litigation"); the results of ACP-01 research, trials, studies and analyses, including the analysis being equivalent to or better than previous research, trials or studies; the receipt of all required regulatory ‎approvals for research, trials or studies; the level of activity, market acceptance and market trends in the healthcare sector; the ‎economy generally; consumer ‎interest in Hemostemix's services and products; competition and ‎Hemostemix's competitive advantages; and Hemostemix obtaining satisfactory financing to ‎ fund Hemostemix's operations including any research, trials or studies, and any Litigation. Forward-looking information is Subject to known and unknown risks, uncertainties and other factors that may cause the actual results, level of activity, performance or achievements of Hemostemix to be materially different from those expressed or implied by such forward-looking information. Such risks and other factors may include, but are not limited to: the ability of Hemostemix to complete clinical trials, complete a satisfactory analyses and results of such analyses to gain regulatory approval of a phase II or phase III clinical trial of ACP-01; potential litigation Hemostemis mayface; general business, economic, competitive, political and social uncertainties; general capital market conditions and market prices for securities; delay or failure to receive board or regulatory approvals; the actual results of future operations including the actual results of future research, trials or studies; competition; changes in legislation ‎affecting Hemostemix; the timing and availability of external financing on acceptable terms; long-term capital requirements and future developments in Hemostemix's markets and the markets in which it expects to compete;‎ lack of qualified, skilled labour or loss of key individuals; and risks ‎related to the COVID-19 pandemic including various recommendations, orders and measures of governmental authorities to ‎try to limit the pandemic, including travel restrictions, border closures, non-essential business closures service disruptions, quarantines, self-isolations, shelters-in-place and social distancing, disruptions to markets, disruptions to economic activity and ‎financings, disruptions to supply chains and sales channels, and a deterioration of general economic conditions including a ‎possible national or global recession or depression;the potential impact that the COVID-19 pandemic may have on Hemostemix which may include a decreased demand for the services that Hemostemix offers; and a deterioration of financial markets that could limit Hemostemix's ability to obtain external financing. A description of additional risk factors that may cause actual results to differ materially from forward-looking information can be found in Hemostemix's disclosure documents on the SEDAR website at . Although Hemostemix has attempted to identify important factors that could cause actual results to differ materially from those contained in forward-looking information, there may be other factors that cause results not to be as anticipated, estimated or intended. Readers are cautioned that the foregoing list of factors is not exhaustive. Readers are further cautioned not to place undue reliance on forward-looking information as there can be no assurance that the plans, intentions or expectations upon which they are placed will occur. Forward-looking information contained in this news release is expressly qualified by this cautionary statement. The forward-looking information contained in this news release represents the expectations of Hemostemix as of the date of this news release and, accordingly, it is Subject to change after such date. However, Hemostemix expressly disclaims any intention or obligation to update or revise any forward-looking information, whether as a result of new information, future events or otherwise, except as expressly required by applicable securities law. To view the source version of this press release, please visit

临床3期细胞疗法

100 项与 ACP-01 相关的药物交易

登录后查看更多信息

研发状态

10 条进展最快的记录,

后查看更多信息

适应症	最高研发状态	国家/地区	公司	日期
心绞痛	临床2期	以色列	Theravitae Co. Ltd.	-
心绞痛	临床2期	泰国	Theravitae Co. Ltd.	-
外周动脉疾病	临床2期	-	Hemostemix Asia, Inc.	-
外周动脉疾病	临床2期	-	Aspire Health Science LLC初创企业	-
外周动脉疾病	临床2期	匈牙利	Theravitae Co. Ltd.	-
血栓闭塞性血管炎	临床2期	-	Hemostemix Asia, Inc.	-
血栓闭塞性血管炎	临床2期	-	Aspire Health Science LLC初创企业	-
血栓闭塞性血管炎	临床2期	加拿大	Hemostemix, Inc.	-
慢性肢体威胁性缺血	临床前	美国	Hemostemix, Inc.	2014-08-01
围手术期缺血	临床前	匈牙利	Salus Ltd.	2008-05-01

登录后查看更多信息

临床结果

适应症

分期

评价

查看全部结果

研究	分期	人群特征	评价人数	分组	结果	评价	发布日期


NCT02551679 (CTgov)	临床2期	慢性肢体威胁性缺血	67	ACP-01 (ACP-01)	製膚憲艱鏇廠鏇艱膚艱(鹽襯積鏇艱襯網餘夢觸) = 積顧憲築蓋網廠簾範簾構夢製網壓蓋網餘艱積 (製顧衊淵鹹醖憲構選積, 願積餘憲襯淵顧觸膚窪 ~ 廠淵淵範積選鏇願獵齋) 更多	-	2023-11-18
				Placebo (Placebo)	製膚憲艱鏇廠鏇艱膚艱(鹽襯積鏇艱襯網餘夢觸) = 窪衊獵觸製鏇築鹹鑰繭構夢製網壓蓋網餘艱積 (製顧衊淵鹹醖憲構選積, 醖顧窪夢網顧願範壓遞 ~ 繭積憲簾簾遞齋淵窪積) 更多
APC01-001 (Pubmed) 人工标引	N/A	心肌疾病	54	ACP-01	(築夢繭廠淵繭遞餘選鹹) = one death (previously unrecognized silent MI), ventricular tachycardia (n = 2) requiring cardioversion, and respiratory infection (n = 2) 衊築廠齋壓窪構鏇鹽簾 (壓衊鏇壓鏇襯製製鏇壓 ) 更多	积极	2023-10-26
				ACP-01 (ischemic subgroup)
NCT02551679 (Corporate Publications) 人工标引	临床2期	心脏衰竭	68	ACP-01	遞糧壓鹹艱簾鹹顧襯餘(築網範鑰壓簾窪繭夢鑰) = 製鏇積積繭艱鑰獵衊積襯憲廠觸憲餘願鏇遞積 (窪積網衊遞衊膚醖構製 )	积极	2022-08-30
				Placebo	遞糧壓鹹艱簾鹹顧襯餘(築網範鑰壓簾窪繭夢鑰) = 艱襯鏇窪製鹹膚憲範鏇襯憲廠觸憲餘願鏇遞積 (窪積網衊遞衊膚醖構製 )