A low-cost automated Gallium-68 drug preparation device for diagnostic PET imaging
用于诊断 PET 成像的低成本自动化 Gallium-68 药物制备设备
基本信息
- 批准号:9347339
- 负责人:
- 金额:$ 22.5万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2017
- 资助国家:美国
- 起止时间:2017-03-02 至 2018-08-31
- 项目状态:已结题
- 来源:
- 关键词:Cancer PatientChemicalsClinicalClinical ResearchClinical trial protocol documentComplexComputersCyclic GMPDetectionDevelopmentDevicesDiagnosisDiagnosticDiagnostic ProcedureDiseaseDrug CompoundingEuropeFOLH1 geneFiltrationFormulationFundingFutureGalliumGeneric DrugsGoalsGrowthHalf-LifeHeatingIndustry StandardInjectableInvestigationInvestigational DrugsLabelLeadLiquid substanceMalignant neoplasm of prostateMaterials TestingMetastatic Neoplasm to the BoneOrphan DrugsPatient CarePatientsPennsylvaniaPeptidesPharmaceutical PreparationsPhasePhase I Clinical TrialsPhonationPositronPositron-Emission TomographyPreparationProcessProductionRadioRadioisotopesRadiopharmaceuticalsReagentRecruitment ActivityRegulationResearchSiteSmall Business Innovation Research GrantSomatostatin ReceptorSterilitySystemTabletsTelephoneTemperatureTestingTimeUnited StatesUniversitiesVacuumbasecostdesignhuman diseasemeetingsnovelnovel diagnosticsnovel therapeuticsoperationpressureprototyperadiochemicalreceptor bindingresponsesuccesstargeted agent
项目摘要
Abstract:
Five Eleven Pharma is developing a simple, low-cost device for automating the preparation of Ga-68 labeled
drugs at any site that is performing PET imaging. The device is being developed to support the broader
creation, distribution, research and use of Ga-68 compounds in diagnostic PET imaging.
There has been a surge in the use of Ga-68-based radiopharmaceuticals throughout the world in the past
several years, particularly in Europe where about 100 centers provide various Ga-68 investigational agents.
The success of these drugs, first of 68Ga-DOTATOC and related somatostatin receptor binding peptides, and
more recently agents targeting prostate cancer such as PSMA-11, is fueling much of this expansion in Europe,
and similar growth is expected in the United States, where DOTATOC received orphan drug status by the US
FDA in 2013. Today, however, only a few academic sites in the US provide all the Ga-68-based drugs needed
to meet patient demand, often through expanded access Investigational New Drug (IND) clinical trial protocols.
In many cases PET imaging with Ga-68 labeled drugs are the best available diagnostic procedure available to
patients for the detection of disease, yet access to these new drugs is limited.
Because of the short half-life (68 min) of Ga-68, it will be difficult for existing radiopharmacy networks (that
were designed for distribution of radiopharmaceuticals with longer half-lives (>= 110 minutes)) to deliver Ga-68
drugs efficiently. On-site preparation of Ga-68 drugs is expected to grow in response to this distribution
problem. Five Eleven will meet this growing demand through a device that will require little expertise to operate
and maintain, and fully automates the process for producing a sterile, injectable Ga-68 radio-labeled drug. The
device will be based on industry-standard, single-use disposable components and will use no externally
connected computer or other device to operate since it will have no changeable operating parameters.
Our aims for the project are to 1) optimize the operating parameters of the device to effectively reduce the
control system and hardware to bare minimums reducing cost significantly (by 10 X) compared to existing
systems. Aim 1 will evaluate fluid drive pressure/vacuum, flow rate and temperature to establish the sensitivity
of the yield and purity of the final product to each of these parameters. 2) Develop a fully automated device
based upon a minimum hardware configuration and fixed control system; and 3) Demonstrate an automated
system by producing 3 Ga-68 compounds P15-041, PSMA-11 and DOTATOC that meet all the quality criteria
required by the FDA for injectable Ga-68 labeled drugs (pH, tonicity, radiochemical purity >90%, radiochemical
identity, Ge-68 content < 0.001%, radionuclidic purity, radionuclidic identity and sterility). Successful
completion of this phase I will lead to full commercial development of a device in phase II with testing in a
clinical study using either proprietary or generic new Ga-68 drugs produced at the clinical PET imaging site.
Page 1 of 1
抽象的:
5-11 Pharma 正在开发一种简单、低成本的设备,用于自动制备 Ga-68 标记的药物
在任何进行 PET 成像的部位使用药物。该设备的开发是为了支持更广泛的
Ga-68 化合物在诊断 PET 成像中的创造、分布、研究和使用。
过去,全球范围内基于 Ga-68 的放射性药物的使用激增
几年来,特别是在欧洲,大约有 100 个中心提供各种 Ga-68 研究药物。
这些药物的成功,首先是 68Ga-DOTATOC 和相关的生长抑素受体结合肽,以及
最近针对前列腺癌的药物,如 PSMA-11,正在很大程度上推动了欧洲的这种扩张,
预计美国也会出现类似的增长,DOTATOC 已获得美国孤儿药地位
2013 年获得 FDA 批准。然而,如今,美国只有少数学术机构提供所需的所有 Ga-68 药物
为了满足患者需求,通常通过扩大研究性新药 (IND) 临床试验方案的访问范围。
在许多情况下,使用 Ga-68 标记药物进行 PET 成像是目前可用的最佳诊断程序。
患者需要检测疾病,但获得这些新药的机会有限。
由于 Ga-68 的半衰期短(68 分钟),现有的放射性药物网络(即
设计用于分配半衰期较长(>= 110 分钟)的放射性药物,以输送 Ga-68
药物有效。 Ga-68 药物的现场制备预计将随着这种分布而增长
问题。 5-11 将通过一种不需要太多专业知识即可操作的设备来满足这种不断增长的需求
并维护并完全自动化生产无菌注射用 Ga-68 放射性标记药物的过程。这
设备将基于行业标准的一次性组件,并且不会使用外部
连接计算机或其他设备进行操作,因为它没有可更改的操作参数。
我们该项目的目标是1)优化装置的运行参数,有效降低
控制系统和硬件达到最低限度,与现有的相比,显着降低成本(降低 10 倍)
系统。目标 1 将评估流体驱动压力/真空、流量和温度以确定灵敏度
最终产品的收率和纯度与每个参数的关系。 2)开发全自动装置
基于最小的硬件配置和固定的控制系统; 3) 展示自动化
系统生产符合所有质量标准的 3 种 Ga-68 化合物 P15-041、PSMA-11 和 DOTATOC
FDA 要求注射用 Ga-68 标记药物(pH、张力、放射化学纯度 >90%、放射化学
同一性、Ge-68 含量 < 0.001%、放射性核素纯度、放射性核素同一性和无菌性)。成功的
第一阶段的完成将导致第二阶段设备的全面商业开发,并在
使用在临床 PET 成像站点生产的专有或通用新 Ga-68 药物进行的临床研究。
第 1 页,共 1 页
项目成果
期刊论文数量(2)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Preliminary Evaluation of 68Ga-P16-093, a PET Radiotracer Targeting Prostate-Specific Membrane Antigen in Prostate Cancer.
68Ga-P16-093(一种针对前列腺癌中前列腺特异性膜抗原的 PET 放射性示踪剂)的初步评估。
- DOI:
- 发表时间:2022-10
- 期刊:
- 影响因子:3.1
- 作者:Lee, Hwan;Scheuermann, Joshua S;Young, Anthony J;Doot, Robert K;Daube;Schubert, Erin K;Fillare, Matthew A;Alexoff, David;Karp, Joel S;Kung, Hank F;Pryma, Daniel A
- 通讯作者:Pryma, Daniel A
[68Ga]Ga-P16-093 as a PSMA-Targeted PET Radiopharmaceutical for Detection of Cancer: Initial Evaluation and Comparison with [68Ga]Ga-PSMA-11 in Prostate Cancer Patients Presenting with Biochemical Recurrence.
[68Ga]Ga-P16-093 作为用于检测癌症的 PSMA 靶向 PET 放射性药物:在出现生化复发的前列腺癌患者中与 [68Ga]Ga-PSMA-11 进行初步评估和比较。
- DOI:
- 发表时间:2020
- 期刊:
- 影响因子:3.1
- 作者:Green, Mark A;Hutchins, Gary D;Bahler, Clinton D;Tann, Mark;Mathias, Carla J;Territo, Wendy;Sims, Justin;Polson, Heather;Alexoff, David;Eckelman, William C;Kung, Hank F;Fletcher, James W
- 通讯作者:Fletcher, James W
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David Alexoff其他文献
David Alexoff的其他文献
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{{ truncateString('David Alexoff', 18)}}的其他基金
Commercialization of a proprietary Ga-68 PSMA-targeted drug for PET imaging in recurrent prostate cancer
用于复发性前列腺癌 PET 成像的专有 Ga-68 PSMA 靶向药物的商业化
- 批准号:
9896923 - 财政年份:2018
- 资助金额:
$ 22.5万 - 项目类别:
Commercialization of a proprietary Ga-68 PSMA-targeted drug for PET imaging in recurrent prostate cancer
用于复发性前列腺癌 PET 成像的专有 Ga-68 PSMA 靶向药物的商业化
- 批准号:
9916719 - 财政年份:2018
- 资助金额:
$ 22.5万 - 项目类别:
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