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Safety, Blood Levels and Effects of AUT00206

2016年10月13日 更新者:Autifony Therapeutics Limited

A Randomised, Double-blind, Placebo-controlled, Single and Repeated Dose Escalation Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AUT00206 in Healthy Volunteers.

The study medicine is a potential future treatment for schizophrenia, an illness that affects the way that people think, feel or behave. It is not clear what causes schizophrenia, but it's been linked to chemical imbalance in the brain. It is hoped that the study medicine will activate specific sites in the brain to help correct that imbalance. Current treatments for schizophrenia don't work very well and can cause unpleasant side effects. It is hoped that the study medicine will work better, and have fewer side effects than existing medicines.

In this 2 part study (Parts A and B), the primary aim is to assess how safe the study medicine is in healthy men, aged 18-45 years, and how much of it gets into the blood. Its effects on the brain will also be tested.

In Part A, up to 24 participants will receive up to 5 single doses of the study medicine (AUT00206 or placebo) by mouth, either after fasting or after a high fat breakfast. The study medicine has never been given to humans before, so the initial doses will be small and the dose level will be increased as the study progresses. Participants may take up to 14 weeks to finish the study. They'll make up to 22 outpatient visits, and stay on the ward up to 5 times, for 3 nights in a row each time.

In Part B, 24 participants will receive daily doses of the study medicine (AUT00206 or placebo) for up to 28 days. Participants will take up to 10 weeks to finish the study. They'll make 6 outpatient visits, and stay on the ward for up to 30 nights, depending on how long we expect it to take until blood levels of the study medicine level off.

A pharmaceutical company, Autifony Therapeutics Limited, is funding the study. The study will take place at 1 centre in London.

研究概览

地位

完全的

干预/治疗

研究类型

介入性

阶段

  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • London、英国、NW10 7EW
        • Hammersmith Medicines Research

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 45年 (成人)

接受健康志愿者

是的

有资格学习的性别

男性

描述

Inclusion Criteria:

  • men aged 18-45 years;
  • body mass index 18.0-30.0 kg/m^2;
  • in good health, as judged by medical history, medical examination, vital signs, ECG and clinical laboratory tests;
  • able to communicate with study personnel; be of sufficient intelligence to understand the nature of the trial; reliable, willing, and likely to comply with the protocol;
  • consent to GP being informed of their participation in the study, and to entering their details into the overvolunteering database (TOPS).

Exclusion Criteria:

  • not healthy (clinically significant abnormality in screening tests, which include ECG, vital signs, physical examination, and laboratory safety tests of blood and urine);
  • severe hearing impairment, or MoCA score of less than 22 points (Part B only);
  • abuse of alcohol or drugs;
  • taken prescription medicine during the 28 days before dosing;
  • taken other medicine (except paracetamol), herbal remedies or dietary supplements during the 7 days before dosing; have had a serious reaction to any medicine, particularly medicines that work in the same way as the study medicine;
  • have had any condition or operation that might affect the way the body absorbs medicines;
  • have had any clinically significant disease;
  • have ever attempted suicide or thought or talked about suicide, using the C-SSRS (Part B only);
  • objection by GP on medical grounds;
  • have donated blood, or taken part in another study, within the past 3 months; or don't agree not to donate blood, or take part in another study, during the 3 months after this study
  • smoking of more than 5 cigarettes daily
  • unwilling to cooperate with the requirements of the protocol

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Number of treatment emergent adverse events
大体时间:Study duration (i.e. up to 14 weeks)
Study duration (i.e. up to 14 weeks)

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2015年9月1日

初级完成 (实际的)

2016年7月1日

研究完成 (实际的)

2016年7月1日

研究注册日期

首次提交

2015年10月15日

首先提交符合 QC 标准的

2015年10月27日

首次发布 (估计)

2015年10月28日

研究记录更新

最后更新发布 (估计)

2016年10月14日

上次提交的符合 QC 标准的更新

2016年10月13日

最后验证

2016年7月1日

更多信息

与本研究相关的术语

其他研究编号

  • AUT011206

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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