A Study to Investigate the Effects of Cleminorexton Compared With Placebo in the Treatment of Participants With Central Disorders of Hypersomnolence
NCT07598708 · Status: NOT_YET_RECRUITING · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 222
Last updated 2026-05-20
Summary
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.
Conditions
Interventions
- DRUG
-
cleminorexton
Oral cleminorexton capsule
- DRUG
-
matching placebo capsule
Sponsors & Collaborators
-
Centessa Pharmaceuticals (UK) Limited
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 70 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-05-15
- Primary Completion
- 2027-09-30
- Completion
- 2027-12-31
- FDA Drug
- Yes
More Related Trials
-
Efficacy Study of EVT 201 in the Treatment of Elderly Patients With Daytime Sleepiness
NCT00401284 ·Status: COMPLETED ·Phase: PHASE2
-
Efficacy and Tolerability of Armodafinil in Adults With Excessive Sleepiness Associated With Shift Work Disorder
NCT01080807 ·Status: COMPLETED ·Phase: PHASE4
-
Expanded Access to SUVN-G3031 (Samelisant) for the Treatment of Subjects With Narcolepsy
NCT05530447 ·Status: NO_LONGER_AVAILABLE
-
A Study to Evaluate the Safety and Efficacy of TS-091 in Patients with Narcolepsy
NCT03267303 ·Status: COMPLETED ·Phase: PHASE2
-
A Phase 3 Study to Evaluate the Efficacy and Safety of Samelisant in Patients With Narcolepsy
NCT07540364 ·Status: NOT_YET_RECRUITING ·Phase: PHASE3
-
Efficacy and Safety of Armodafinil for Adults With Excessive Sleepiness Obstructive Sleep Apnea/Hypopnea and Depression
NCT00518986 ·Status: COMPLETED ·Phase: PHASE4
-
Study to Investigate Safety, Tolerability, Pharmacokinetics and Cardiac Function After Repeat Doses of SB-649868 in Healthy-volunteers
NCT01030939 ·Status: COMPLETED ·Phase: PHASE1
-
A Study of TAK-360 in Adults With Idiopathic Hypersomnia
NCT06812078 ·Status: RECRUITING ·Phase: PHASE2
-
Study of the Effect of Armodafinil Treatment in Healthy Subjects With Excessive Sleepiness Associated With Jet Lag Disorder
NCT00758498 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Evaluate the Safety and Effectiveness of ALKS 2680 in Subjects With Idiopathic Hypersomnia
NCT06843590 ·Status: RECRUITING ·Phase: PHASE2
-
A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of JNJ-48816274
NCT02852395 ·Status: COMPLETED ·Phase: PHASE1
-
A Study of Daridorexant in Chinese Patients With Insomnia Disorder
NCT06010693 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of TAK-925 in Healthy Volunteers and Participants With Narcolepsy
NCT03748979 ·Status: COMPLETED ·Phase: PHASE1
-
A Phase 3 Study to Assess the Safety and Efficacy of Pitolisant in Adult Patients With Idiopathic Hypersomnia
NCT05156047 ·Status: COMPLETED ·Phase: PHASE3
-
Safety and Efficacy Study of Armodafinil (CEP-10953) in the Treatment of Excessive Sleepiness Associated With Narcolepsy
NCT00078377 ·Status: COMPLETED ·Phase: PHASE3
-
Study of the Insomnia in Patients With Low Back Pain
NCT00365976 ·Status: COMPLETED ·Phase: PHASE4
-
Clarithromycin for the Treatment of Hypersomnia
NCT01146600 ·Status: COMPLETED ·Phase: PHASE2
-
Adult Polysomnography Primary Insomnia Cross Over Study (0928-049)(TERMINATED)
NCT00420810 ·Status: TERMINATED ·Phase: PHASE3
-
Sodium Oxybate in Idiopathic Hypersomnia
NCT03597555 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Almorexant (ACT-078573) in Elderly Subjects With Chronic Primary Insomnia
NCT00606593 ·Status: COMPLETED ·Phase: PHASE2
-
A Study to Evaluate the Efficacy and Safety of E2086 in Adults With Narcolepsy
NCT07493265 ·Status: RECRUITING ·Phase: PHASE2
-
Safety/Efficacy Study With Armodafinil (CEP-10953) in Treatment of Excessive Sleepiness Associated With Chronic SWSD
NCT00080288 ·Status: COMPLETED ·Phase: PHASE3
-
Study to Assess Patient Reported Outcomes With Armodafinil Treatment for Excessive Sleepiness in Adults With Narcolepsy or Obstructive Sleep Apnea/Hypopnea Syndrome
NCT00228566 ·Status: COMPLETED ·Phase: PHASE3
-
Phase Ⅰb/Ⅱ Study of HS-10506 in Chinese Participants With Insomnia Disorder
NCT06279286 ·Status: NOT_YET_RECRUITING ·Phase: PHASE1/PHASE2
-
Safety and Efficacy of FT218 in Idiopathic Hypersomnia (REVITALYZ)
NCT06525077 ·Status: COMPLETED ·Phase: PHASE3