PHARMACEUTICS/FORMULATION/CMC CONSULTING SERVICES FOR NINDS HEAL PROGRAM

NINDS HEAL 计划的药剂/制剂/CMC 咨询服务

• 批准号: 10825428
• 负责人: SOMNATH MISHRA
• 金额: $ 4.28万
• 依托单位国家: 美国
• 财政年份: 2021
• 资助国家: 美国
• 起止时间: 2021-09-29 至 2024-09-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10825428
• 关键词: Authorization documentation; Chemicals; Chemistry; Chronic; Clinical Research; Conduct Clinical Trials; Contracts; Development; Dose; Drug Kinetics; Electronic Mail; Ensure; European; Experimental Designs; Feedback; Formulation; Guidelines; Helping to End Addiction Long-term; Human; International; Investigational Drugs; Knee Osteoarthritis; Lead; Marketing; Medicine; Methodology; National Institute of Neurological Disorders and Stroke; Opiate Addiction; Pain; Pain management; Perioperative; Pharmaceutical Preparations; Pharmacologic Substance; Pharmacy (field); Preparation; Process; Quality of life; Recommendation; Reporting; Research Contracts; Risk; Role; Science; Services; Speed; Telephone; United States National Institutes of Health; Visit; analytical method; assay development; authority; chronic musculoskeletal pain; clinical pain; design; drug metabolism; improved; lead optimization; manufacture; member; method development; novel; product development; programs; small molecule; symposium

This study is part of the NIH’s Helping to End Addiction Long-term (HEAL) initiative to speed scientific solutions to understand the basis of pain and enhance clinical pain management. CMC / Pharmaceutics / Formulation CMC / Pharmaceutics / Formulation consultants will be expected to provide senior-level CMC / Pharmaceutics / Formulation expertise and contribute feedback and guidance on projects to the NIH and to LDT members through conference calls and by email. The role of the CMC / Pharmaceutics / Formulation consultant may include but is not limited to the following responsibilities and tasks: • Evaluate Chemical Manufacturing and Controls [CMC] activities for compounds under development in accordance with US regulatory and International Council of Harmonization for Registration of Pharmaceuticals for Human Use [ICH] guidelines. • Identify and assess regulatory risks for compounds under development and provide CMC guidance to NINDS and LDTs. Develop CMC strategies which accord with US and international guidelines. • Provide recommendations for drug substance manufacturing, analytical method development, and process development for small molecules. • Provide pharmaceutical sciences expertise in chemical manufacturing, formulation, and product development for small molecules. • Assist in ensuring timely preparation, review, and submission of chemical manufacturing and controls documents to regulatory authorities including FDA, European Medicines Agency [EMA] and other national authorities, to support the conduct of clinical trials and marketing applications. • Provide expertise in activities related to API development. • Recommend dose form selection and API development strategies for NINDS efforts. • Develop plans to assist NIH staff in strategically managing chemical manufacturing and controls pharmacokinetic programs which facilitate assay development, exploratory chemistry, lead optimization, formulation activities, investigational new drug (IND) enabling, and clinical studies. • Accompany NIH staff or visit, at NIH staff request, Contract Research Organizations [CRO] under contract with NIH. Inspect facilities and discuss appropriateness of CRO proposed methodology. Submit trip reports to NIH staff. • Assist NIH staff to design investigative chemical manufacturing and controls pharmacokinetics studies, including study strategy and experimental design. Provide advice regarding recommended study milestones and prepare milestone reports as needed. • Facilitate Lead Development Team discussions via telephone and email regarding assigned drug metabolism and pharmacokinetics efforts. This study is part of the NIH’s Helping to End Addiction Long-term (HEAL) initiative to speed scientific solutions to understand the basis of pain and enhance clinical pain management. It’s part of the program that establishes novel treatment options for a variety of pain conditions to improve quality of life and reduce opioid dependency. The program studies a broad range of pain conditions, including chronic overlapping pain conditions, chronic musculoskeletal pain, perioperative pain, and knee osteoarthritis.

这项研究是NIH帮助结束长期成瘾（HEAL）计划的一部分，旨在加速科学解决方案，以了解疼痛的基础并加强临床疼痛管理。 CMC /药剂学/制剂 CMC /药剂学/制剂顾问将提供高级CMC /药剂学/制剂专业知识，并通过电话会议和电子邮件向NIH和LDT成员提供有关项目的反馈和指导。CMC /药剂学/制剂顾问的职责可能包括但不限于以下职责和任务： · 根据美国法规和人用药品注册国际协调理事会[ICH]指导原则，评价正在开发的化合物的化学生产和控制[CMC]活动。 · 识别和评估正在开发的化合物的监管风险，并为NINDS和LDT提供CMC指导。制定符合美国和国际指导方针的雅阁。 · 为小分子原料药生产、分析方法开发和工艺开发提供建议。 · 在化学品制造、配方和小分子产品开发方面提供制药科学专业知识。 · 协助确保及时准备、审查并向监管机构（包括FDA、欧洲药品管理局[EMA]和其他国家机构）提交化学品生产和控制文件，以支持临床试验和上市申请的开展。 · 提供API开发相关活动的专业知识。 · 为NINDS工作推荐剂型选择和API开发策略。 · 制定计划，协助NIH工作人员战略性地管理化学品生产和控制药代动力学计划，以促进检测开发、探索性化学、先导化合物优化、制剂活动、研究性新药（IND）启用和临床研究。 · 陪同NIH工作人员或应NIH工作人员要求访问与NIH签订合同的合同研究组织[CRO]。检查设施并讨论CRO提议方法的适当性。向NIH工作人员提交旅行报告。 · 协助NIH人员设计研究性化学品生产和控制药代动力学研究，包括研究策略和实验设计。根据需要，提供关于推荐研究里程碑的建议并准备里程碑报告。 · 通过电话和电子邮件促进首席开发团队讨论分配的药物代谢和药代动力学工作。 这项研究是NIH帮助结束长期成瘾（HEAL）计划的一部分，旨在加速科学解决方案，以了解疼痛的基础并加强临床疼痛管理。这是该计划的一部分，该计划为各种疼痛状况建立了新的治疗方案，以改善生活质量并减少阿片类药物依赖。 该计划研究了广泛的疼痛状况，包括慢性重叠疼痛状况，慢性肌肉骨骼疼痛，围手术期疼痛和膝关节骨关节炎。