QSAM Biosciences Expands Its Study of CycloSam in the Treatment of Bone Cancer; Opens Patient Enrollment at Key Chicago Center, Insight Hospital and Medical Center
QSAM Biosciences Expands Its Study of CycloSam in the Treatment of Bone Cancer; Opens Patient Enrollment at Key Chicago Center, Insight Hospital and Medical Center
Austin, TX, May 23, 2023 (GLOBE NEWSWIRE) -- QSAM Biosciences Inc. (OTCQB: QSAM), a company developing next generation therapeutic radiopharmaceuticals, including Samarium-153-DOTMP (CycloSam), for the treatment of bone cancer and other diseases and conditions, today announces the addition of the Insight Research Institute at the Insight Hospital and Medical Center in Chicago, IL, as a clinical trial site approved to begin enrolling participants into the Phase 1 study evaluating CycloSam in patients with multiple types of bone cancer that either originated in or has metastasized to the bone.
德克萨斯州奥斯汀,2023 年 5 月 23 日(GLOBE NEWSWIRE)— QSAM Biosciences Inc.(OTCQB: QSAM),一家开发下一代治疗性放射性药物的公司,包括 samarium-153-dotMP(cyclosam),用于治疗骨癌和其他疾病和病症,今天宣布在伊利诺伊州芝加哥的Insight医院和医疗中心增加Insight研究所,作为临床试验场所,获准开始招募参与者参加评估 CycloSam 的 1 期研究 患有多种类型的骨癌的患者,这些骨癌要么起源于骨骼,要么已经转移到骨骼。
QSAM's study is a multiple center, open label, dose escalation clinical trial intended to determine the maximum tolerated dose of CycloSam in patients, as well as assess early efficacy signals. Patients with bone cancer that has metastasized from the breast, lungs, prostate or other organs, as well as patients with cancer that has originated in the bone such as osteosarcoma and Ewing's Sarcoma – diseases that mostly affect children and young adults -- may be eligible.
QSAM 的研究是一项多中心、开放标签、剂量递增的临床试验,旨在确定 CycloSam 的最大耐受剂量 在患者身上,以及评估早期疗效信号。从乳房、肺部、前列腺或其他器官转移的骨癌患者,以及源自骨骼的癌症患者,例如骨肉瘤和尤因氏肉瘤(主要影响儿童和年轻人的疾病),可能符合资格。
"We are pleased to be working with the excellent team at Insight Hospital and Medical Center to continue the expansion of our drug development program for CycloSam in the large population center of Chicago," stated Douglas R. Baum, CEO and co-founder of QSAM. "We expect the addition of this fourth clinical trial site will help advance our study, and it also constitutes the initial site that will be serviced through our recently announced partnership with the leading nuclear pharmacy network, Radioisotope Life Sciences, RLS."
“我们很高兴能与Insight Hospital and Medical Center的优秀团队合作,继续扩大我们的CycloSam药物开发计划 在芝加哥人口稠密的中心,” QSAM首席执行官兼联合创始人道格拉斯·鲍姆说。“我们预计,第四个临床试验基地的增加将有助于推进我们的研究,它也是我们最近宣布的与领先的核药房网络Radiosope Life Sciences,RLS的合作伙伴关系将为其提供服务的初始站点。”
"Metastatic bone cancer is often life threatening and remains an area of high unmet medical need for patients with limited treatment options that are often ineffective," stated Mohammed T. Hussain, MD, an Oncologist and the Investigator at Insight Hospital and Medical Center. "Therapeutic radiopharmaceuticals like CycloSam represent a novel and potentially important treatment option for patients suffering from this debilitating and deadly disease."
Insight Hospital and Medical Center肿瘤学家兼研究员穆罕默德·侯赛因医学博士说:“转移性骨癌通常危及生命,对于治疗选择有限且往往无效的患者来说,转移性骨癌仍然是医疗需求高度未得到满足的领域。”“像 CycloSam 这样的治疗性放射性药物 对于患有这种使人衰弱和致命的疾病的患者来说,这是一种新颖且可能重要的治疗选择。”
About QSAM Biosciences
QSAM Biosciences, Inc. is developing next-generation nuclear medicines for the treatment of cancer and other diseases. QSAM's initial technology, CycloSam (Samarium-153 DOTMP), is a clinical-stage bone-targeting radiopharmaceutical developed by IsoTherapeutics Group LLC, pioneers in the nuclear medicine space who also developed the FDA-approved Quadramet (Samarium-153 EDTMP), which is indicated for bone cancer pain palliation. QSAM is led by an experienced executive team and board of directors that have completed numerous FDA approvals and multiple successful biotech exits.
关于 QSAM 生物科学
QSAM Biosciences, Inc. 正在开发用于治疗癌症和其他疾病的下一代核药物。QSAM 最初的技术 CycloSam (Samarium-153 DOTMP)是一种临床阶段的骨靶向放射性药物,由核医学领域的先驱Isotherapeutics Group LLC开发,他还开发了美国食品药品管理局批准的Quadramet (Samarium-153 EDTMP),适用于缓解骨癌疼痛。QSAM由经验丰富的管理团队和董事会领导,他们已经完成了许多FDA的批准和多次成功的生物技术退出。
CycloSam is currently being studied in an open-label, dose escalating Phase 1 safety study at four clinical trial sites in the United States, with a focus on bone cancer that has metastasized from the breast, lung, prostate or other organs. The drug candidate has demonstrated preliminary safety and efficacy in animal studies and a single patient FDA-cleared human trial performed in 2020 at the Cleveland Clinic. QSAM has also received Orphan Drug and Rare Pediatric Disease Designations from the FDA for the indication of osteosarcoma, a disease that mostly affects children and young adults.
cyclo 目前正在美国四个临床试验场所进行一项开放标签、剂量递增的1期安全性研究中进行研究,重点是从乳房、肺部、前列腺或其他器官转移的骨癌。该候选药物已在动物研究中显示出初步的安全性和有效性,并于2020年在克利夫兰诊所进行了一项经美国食品药品管理局批准的单一患者人体试验。QSAM还因骨肉瘤的适应症而获得了美国食品药品管理局颁发的孤儿药和罕见儿科疾病称号,骨肉瘤是一种主要影响儿童和年轻人的疾病。
CycloSam uses a patented formulation of low specific activity Samarium-153 (resulting in far less long-lived europium impurities) and DOTMP, a chelator that targets sites of high bone turnover and is believed to reduce or eliminate off-target migration, making it, in management's opinion based on scientific data, an ideal agent to treat primary and secondary bone cancers. Through the carrier vehicle DOTMP, CycloSam delivers targeted radiation selectively to the skeletal system with high uptake adjacent to areas of bone tumors where the beta-emitting Samarium-153 can irradiate and potentially destroy cancer cells. Because of CycloSam's mechanism of action and demonstrated safety profile to date, it is also believed to be a candidate for effectiveness trials in bone marrow ablation as preconditioning for stem cell transplantation, as well as in procedures to reduce external beam radiation to bone tumors. Further, CycloSam utilizes a streamlined, just-in-time manufacturing process that is already significantly in place. Given these factors, management believes there is a strong pathway to commercialization for CycloSam.
cyclo 使用低比活性Samarium-153的专利配方(因此寿命要短得多)和DOTMP,DOTMP是一种针对骨更新率高的部位的螯合剂,据信可以减少或消除偏离目标的迁移,根据科学数据,管理层认为它是治疗原发性和继发性骨癌的理想药物。通过载具 DOTMP,cycloSam 选择性地向骨骼系统提供有针对性的辐射,在骨肿瘤区域附近,释放β的Samarium-153可以照射并可能摧毁癌细胞。由于CycloSam的作用机制和迄今为止已证明的安全性,它也被认为是骨髓消融作为干细胞移植预处理的有效性试验的候选药物,也是减少对骨肿瘤的外部光束辐射的手术的有效性试验的候选药物。此外,cyclosam 采用了简化、准时的制造流程,该流程已经显著到位。鉴于这些因素,管理层认为 CycloSam 有很强的商业化途径。
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Corporate Communications
ir@qsambio.com
Namrata Chand, VP-Operations
企业传播
ir@qsambio.com
Namrata Chand,运营副总裁