ORX750 for Narcolepsy and Idiopathic Hypersomnia
(CRYSTAL-1 Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests a new treatment called ORX750, designed to reduce daytime sleepiness in people with narcolepsy and idiopathic hypersomnia (IH). The trial evaluates the safety of ORX750 and its effects on these conditions, which cause excessive daytime sleepiness (EDS) and, in some cases, sudden muscle weakness (cataplexy). Participants will receive either ORX750 or a placebo (a pill with no active medication) for comparison. Individuals diagnosed with Narcolepsy Type 1, Narcolepsy Type 2, or IH who are willing to stop their current medications might be suitable for this study. As a Phase 2 trial, this research focuses on assessing the treatment's effectiveness in an initial, smaller group, allowing participants to contribute to significant advancements in treatment.
Will I have to stop taking my current medications?
Yes, you will need to stop taking all medications used for treating narcolepsy or idiopathic hypersomnia to participate in this trial.
Is there any evidence suggesting that ORX750 is likely to be safe for humans?
Research shows that ORX750 is a new treatment being tested for people with narcolepsy and idiopathic hypersomnia. Early studies have examined the safety of ORX750 in humans. Initial results suggest that most participants did not experience serious side effects, indicating the treatment is generally well-tolerated.
ORX750 is designed to mimic orexin, a brain protein that helps maintain wakefulness during the day. Although more research is needed, the current phase of testing suggests that ORX750 is promising in terms of safety. This stage of research typically checks for serious side effects and helps determine how the treatment affects the body.
For those considering joining a trial, this information may provide insight into the safety of ORX750. Always consult a healthcare provider to discuss any concerns or questions about participating in a clinical trial.12345Why do researchers think this study treatment might be promising for narcolepsy and idiopathic hypersomnia?
Most treatments for narcolepsy and idiopathic hypersomnia typically focus on stimulating the central nervous system to reduce excessive daytime sleepiness. However, ORX750 works differently by targeting the orexin system, which plays a crucial role in regulating wakefulness and sleep. This new mechanism of action is what excites researchers, as it has the potential to address the root cause of these sleep disorders more directly than current stimulant-based therapies. Additionally, ORX750 may offer a more targeted approach with possibly fewer side effects compared to traditional treatments like modafinil or amphetamines.
What evidence suggests that ORX750 might be an effective treatment for narcolepsy and idiopathic hypersomnia?
Research has shown that ORX750, a new treatment under study in this trial, appears promising for individuals with narcolepsy and idiopathic hypersomnia. In earlier studies, ORX750 helped participants stay awake longer during the day. Specifically, it increased the time it took for participants to fall asleep by more than 10 minutes compared to a placebo. Additionally, ORX750 was well tolerated, with most participants experiencing no major side effects. This trial will evaluate ORX750 in separate arms for narcolepsy type 1, narcolepsy type 2, and idiopathic hypersomnia. These early results suggest that ORX750 could help reduce excessive daytime sleepiness in these conditions.13467
Are You a Good Fit for This Trial?
This trial is for adults aged 18-65 with a BMI between 17 and 37 who have narcolepsy or idiopathic hypersomnia. Participants must be able to follow the study rules and stop taking their current narcolepsy or hypersomnia meds. They can't join if they have serious health issues like heart, lung, liver diseases, or other conditions causing excessive sleepiness.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive ORX750 or placebo to evaluate safety, tolerability, pharmacokinetics, and pharmacodynamics
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- ORX750
Find a Clinic Near You
Who Is Running the Clinical Trial?
Centessa Pharmaceuticals (UK) Limited
Lead Sponsor