Testing of a Novel Inhaled Clofazimine (CFZ) Dry Powder Formulation in a Mouse Model of Mycobacterium tuberculosis

在结核分枝杆菌小鼠模型中测试新型吸入氯法齐明 (CFZ) 干粉制剂

• 批准号: 10927007
• 负责人: JANICE ENDSLEY
• 金额: $ 68万
• 依托单位: UNIVERSITY OF TEXAS MED BR GALVESTON
• 依托单位国家: 美国
• 财政年份: 2023
• 资助国家: 美国
• 起止时间: 2023-08-01 至 2025-03-31
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10927007
• 关键词: Acquired Immunodeficiency Syndrome; Basic Science; Clinical Trials; Collaborations; Communities; Contracts; Development; Devices; Drug Kinetics; Dryness; Extramural Activities; Formulation; HIV; Hepatitis B Virus; Hepatitis C virus; Inbred BALB C Mice; Inhalation; Investigational New Drug Application; Investigator-Initiated Research; Lecithin; Licensure; Mus; Mycobacterium tuberculosis; Mycobacterium tuberculosis complex; National Institute of Allergy and Infectious Disease; Powder dose form; Private Sector; Research; Resources; Services; Testing; Therapeutic; Tuberculosis; United States Food and Drug Administration; Work; efficacy study; in vivo; mouse model; novel; novel therapeutics; pre-clinical; product development; repository; research clinical testing; research study; therapeutic development

Preclinical Services for HIV Therapeutics: The purpose of these Indefinite Delivery/Indefinite Quantity contracts is to provide the extramural scientific community with research materials and preclinical product development support for candidate products that emerge from investigator-initiated research studies or from collaborations with private sector or academic partners. The scope of work encompasses activities that range from basic research and initial product discovery to activities required for clinical trials and/or product licensure. These services may also be used to support product discovery and development leading to Investigational New Drug Application (IND), Investigational Device Exemption (IDE), and/or New Drug Application (NDA) filings with the Food and Drug Administration (FDA). NIAID Division of AIDS will primarily use these contracts to fill critical development and resource gaps more rapidly and efficiently and advance promising products into clinical testing. The focus of these contracts will be development of therapeutic products for human immunodeficiency virus (HIV), hepatitis B virus (HBV), hepatitis C virus (HCV), and Mycobacterium tuberculosis (MTB) complex, as well as repository services. The purpose of this Task Order is to test a novel inhaled Clofazimine (CFZ) dry powder formulation in a mouse model of Mycobacterium tuberculosis.

HIV 治疗的临床前服务：这些无限期交付/无限数量合同的目的是为校外科学界提供研究材料和临床前产品开发支持，以支持研究者发起的研究或与私营部门或学术界合作产生的候选产品。合作伙伴。工作范围涵盖从基础研究和初始产品发现到临床试验和/或产品许可所需的活动。这些服务还可用于支持产品发现和开发，从而向食品和药物管理局 (FDA) 提交研究性新药申请 (IND)、研究性器械豁免 (IDE) 和/或新药申请 (NDA)。 NIAID 艾滋病部门将主要利用这些合同来更快、更有效地填补关键的开发和资源缺口，并将有前景的产品推进临床测试。这些合同的重点将是开发针对人类免疫缺陷病毒（HIV）、乙型肝炎病毒（HBV）、丙型肝炎病毒（HCV）和结核分枝杆菌（MTB）复合体的治疗产品以及储存库服务。该任务单的目的是在结核分枝杆菌小鼠模型中测试新型吸入氯法齐明 (CFZ) 干粉制剂。