Department of Psychiatry and Behavioral Sciences, University of Minnesota, Minneapolis, MN, USA.
Holland Bloorview Kids Rehabilitation Hospital, University of Toronto, Toronto, ON, Canada.
Mol Autism. 2022 Jun 11;13(1):25. doi: 10.1186/s13229-022-00505-6.
Autism spectrum disorder (ASD) is a common and heterogeneous neurodevelopmental condition that is characterized by the core symptoms of social communication difficulties and restricted and repetitive behaviors. At present, there is an unmet medical need for therapies to ameliorate these core symptoms in order to improve quality of life of autistic individuals. However, several challenges are currently faced by the ASD community relating to the development of pharmacotherapies, namely in the conduct of clinical trials. Balovaptan is a V1a receptor antagonist that has been investigated to improve social communication difficulties in individuals with ASD. In this viewpoint, we draw upon our recent first-hand experiences of the balovaptan clinical development program to describe current challenges of ASD trials.
The balovaptan trials were conducted in a wide age range of individuals with ASD with the added complexities associated with international trials. When summarizing all three randomized trials of balovaptan, a placebo response was observed across several outcome measures. Placebo response was predicted by greater baseline symptom severity, online recruitment of participants, and less experienced or non-academic trial sites. We also highlight challenges relating to selection of outcome measures in ASD, the impact of baseline characteristics, and the role of expectation bias in influencing trial results.
Taken together, the balovaptan clinical development program has advanced our understanding of the key challenges facing ASD treatment research. The insights gained can be used to inform and improve the design of future clinical trials with the collective aim of developing efficacious therapies to support individuals with ASD.
自闭症谱系障碍(ASD)是一种常见且具有异质性的神经发育障碍,其特征是存在社交沟通困难和受限及重复行为等核心症状。目前,人们迫切需要治疗方法来改善这些核心症状,以提高自闭症患者的生活质量。然而,自闭症领域目前面临着与开发药物治疗相关的一些挑战,特别是在临床试验的开展方面。巴洛沙韦坦是一种 V1a 受体拮抗剂,已被研究用于改善自闭症患者的社交沟通困难。在本观点文章中,我们借鉴了我们最近在巴洛沙韦坦临床开发项目中的第一手经验,描述了当前自闭症试验所面临的挑战。
巴洛沙韦坦试验在 ASD 患者的广泛年龄范围内进行,同时还涉及国际试验的额外复杂性。当总结巴洛沙韦坦的所有三项随机试验时,观察到几种结局测量指标均出现安慰剂反应。安慰剂反应可由更大的基线症状严重程度、参与者的在线招募以及经验较少或非学术性试验地点来预测。我们还强调了在 ASD 中选择结局测量指标、基线特征的影响以及期望偏差在影响试验结果方面的挑战。
综上所述,巴洛沙韦坦的临床开发项目加深了我们对自闭症治疗研究所面临关键挑战的理解。所获得的见解可用于为未来临床试验的设计提供信息和改进,以共同开发有效的治疗方法来支持自闭症患者。