Incorporating Patient Input into the Target Product Profile.

IF 1.9 4区 医学 Q4 MEDICAL INFORMATICS
Jean-Noel Talabardon, Janet E Church, Masanori Okuse, Michaela Dinboeck, Sheila Dickinson, Simon Messner, Michael Boisclair, Jean-Pierre Malkowski
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Abstract

Target product profiles (TPP) are summaries of characteristics which drug developers expect to be necessary for a product to meet patients' needs, receive regulatory and payer approval, and differ from existing treatment options. As the experts on their own disease, patients bring invaluable perspectives to drug development, which cannot be obtained by other means. This communication reports on the development of a systematic guidance framework for a patient-focused, standardized TPP. The guidance was developed in a long-term iterative process, with crucial aspects reviewed and validated with the patient community. Five focus areas of a TPP were identified where patient perspectives are fundamental: target population, unmet need, dosage frequency and route of administration, efficacy endpoints, and acceptability of benefit/risk profile trade-offs. A guiding principle should be to incorporate patient perspectives in a systematic process starting as early as possible. A number of tools are available for obtaining patient perspectives, e.g., desk research, patient advisory boards/patient councils/online bulletin boards, focus groups with patients/caregivers, and/or in-depth interviews. When discussing the proposed process with patient representatives, they identified several key requirements for the interaction between R&D organizations and patient representatives. These include the use of clear language, respect for patients, engagement with patient experts, provision of adequate context and background information. We further discuss the relative importance of integrating patient perspectives into the different focus areas and touch upon the potential benefits to patient organizations from adapting these concepts and processes to enhance their voices in drug development.

Abstract Image

Abstract Image

将患者输入纳入目标产品简介。
目标产品概况(TPP)是药物开发人员期望产品满足患者需求、获得监管部门和付款人批准以及与现有治疗方案不同的必要特征的总结。患者作为自身疾病的专家,为药物开发带来了宝贵的视角,这是其他途径无法获得的。本通报报告了为以患者为中心的标准化跨太平洋伙伴关系制定系统指导框架的情况。该指南是在一个长期反复的过程中制定的,对关键方面进行了审查,并与患者社区进行了验证。确定了TPP的五个重点领域,其中患者观点是基本的:目标人群、未满足的需求、给药频率和给药途径、疗效终点以及获益/风险权衡的可接受性。指导原则应该是尽早开始将患者的观点纳入系统过程。有许多工具可用于获取患者观点,例如,案头研究、患者咨询委员会/患者委员会/在线公告板、患者/护理人员焦点小组和/或深度访谈。当与患者代表讨论拟议的流程时,他们确定了研发组织与患者代表之间互动的几个关键要求。其中包括使用清晰的语言,尊重患者,与患者专家接触,提供充分的背景和背景信息。我们进一步讨论将患者观点整合到不同重点领域的相对重要性,并触及患者组织通过调整这些概念和过程来增强他们在药物开发中的发言权的潜在好处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Therapeutic innovation & regulatory science
Therapeutic innovation & regulatory science MEDICAL INFORMATICS-PHARMACOLOGY & PHARMACY
CiteScore
3.40
自引率
13.30%
发文量
127
期刊介绍: Therapeutic Innovation & Regulatory Science (TIRS) is the official scientific journal of DIA that strives to advance medical product discovery, development, regulation, and use through the publication of peer-reviewed original and review articles, commentaries, and letters to the editor across the spectrum of converting biomedical science into practical solutions to advance human health. The focus areas of the journal are as follows: Biostatistics Clinical Trials Product Development and Innovation Global Perspectives Policy Regulatory Science Product Safety Special Populations
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