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临床试验/NCT07598708
NCT07598708招募中2 期

A Randomized, Double-blind, 3-Arm Parallel Design Study to Investigate the Efficacy, Safety, Tolerability, and Pharmacokinetics of Cleminorexton Compared With Placebo in Participants With Central Disorders of Hypersomnolence

Centessa Pharmaceuticals (UK) Limited20 个研究点 分布在 1 个国家目标入组 222 人开始时间: 2026年5月29日最近更新:
干预措施

试验速览

阶段
2 期
状态
招募中
入组人数
222
试验地点
20

研究概览

简要总结

Narcolepsy Type 1 (NT1) and Narcolepsy Type 2 (NT2) are rare conditions that make people feel very sleepy during the day (often referred to as excessive daytime sleepiness [EDS]). People living with these conditions might find it hard to stay alert and pay attention when they are at school, working, driving, or performing other daily activities.

While all conditions result in feeling sleepy, there are some differences in other common symptoms:

  • NT1: People with NT1 often feel very tired during the day and experience cataplexy. Cataplexy is a sudden loss of muscle strength, which can cause someone to collapse or lose control of their muscles for a short time. This is often triggered by strong emotions, such as laughter or surprise. They may also have trouble sleeping well at night.
  • NT2: People with NT2 feel sleepy during the day, just like NT1, but they do not have cataplexy.

Orexin is a protein in the brain that helps coordinate a system that plays an important role in helping people to stay awake during the daytime. Cleminorexton is designed to mimic the action of orexin. The purpose of this study is to see how safe and tolerable cleminorexton is in NT1 and NT2 and learn about what the drug does to the body. Another goal of the study is to see if cleminorexton can help people with NT1 and NT2 feel less sleepy and make other symptoms better.

详细描述

The SAPPHIRE Clinical Trial

The Sponsor may in the future, through a protocol amendment, expand the protocol to include participants with idiopathic hypersomnia (IH) in Cohort C.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 18-70 years of age
  • Body Mass Index (BMI) within the range ≥ 17.0 and ≤ 45 kg/m^2 (inclusive)
  • Meets the diagnostic criteria of Narcolepsy Type 1 (NT1) or Type 2 (NT2) according to International Classification of Sleep Disorders, 3rd edition, Text Revision edition (ICSD-3-TR) criteria
  • Is willing and able to discontinue all medications used for the treatment of narcolepsy
  • Is willing and able to adhere to additional protocol requirements

排除标准

  • Medical disorder other than NT1 or NT2, that is associated with excessive daytime sleepiness (EDS)
  • Presence of significant cardiovascular, pulmonary, gastrointestinal, hepatic, renal, hematological, malignancy, endocrine, neurological or psychiatric disease

研究组 & 干预措施

Group A - Narcolepsy Type 1 (placebo)

Placebo Comparator

干预措施: Placebo (Drug)

Group B - Narcolepsy Type 2 (Dose 1)

Experimental

干预措施: cleminorexton (Drug)

Group A - Narcolepsy Type 1 (Dose 1)

Experimental

干预措施: cleminorexton (Drug)

Group A - Narcolepsy Type 1 (Dose 2)

Experimental

干预措施: cleminorexton (Drug)

Group B - Narcolepsy Type 2 (placebo)

Placebo Comparator

干预措施: Placebo (Drug)

Group B - Narcolepsy Type 2 (Dose 2)

Experimental

干预措施: cleminorexton (Drug)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (20)

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