Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Idorsia Pharmaceuticals Ltd.
Age
10–17
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Signed and dated informed consent form (ICF) from the caregiver, i.e., parent/legal guardian prior to any study mandated procedure, or as per local regulation.
Written assent must be obtained from subjects of the appropriate age who can give assent, as determined by the caregiver and local regulation or institutional review boards / independent ethics committees.
Male or female subjects aged ≥ 10 and \< 18 years at the time of signing the ICF.
Chronic insomnia disorder in accordance with International Classification of Sleep Disorders, 3rd edition (ICSD-3) or insomnia disorder in accordance with Diagnostic and Statistical Manual of Mental Disorders, 5th edition (DSM-5) criteria at Screening, as supported by statements from the child and/or the caregiver:
1. Difficulty initiating or maintaining sleep, or early morning awakening with inability to return to sleep,
2. Sleep difficulty has been present for at least 3 months prior to Screening,
3. Sleep difficulty occurs at least 3 nights per week,
4. Persistence of sleep difficulty, despite adequate sleep hygiene or non-pharmacological therapy,
5. The sleep problem occurs despite adequate age appropriate time and opportunity for sleep,
6. The sleep problem is not due to the direct pharmacological effects of any concomitant medication (e.g., amphetamines, selective serotonin reuptake inhibitors) as per investigator judgment,
7. Self-report or caregiver report of poor sleep quality and/or quantity impacting the daytime performance of the subject,
Sleep Disturbance Scale for Children score \> 16 on the Difficulty Initiating or Maintaining Sleep domain at Screening.
Adolescent of Child-Bearing Potential:
1. Negative serum pregnancy test at Screening and a negative urine pregnancy test at Randomization.
2. Agreement to undertake urine pregnancy tests during the study, as per the schedule of activities and up to 5 days after study treatment discontinuation.
3. Agreement to use an acceptable effective method of contraception from Screening up to 5 days after study treatment discontinuation.
You may not be if
Body weight \< 25 kg.
Daytime napping ≥ 1 h per day on at least 3 weekdays per week during the 3 months prior to Screening.
Any lifetime history of sleep-related breathing disorders such as obstructive sleep apnea, based on the subject's medical records. Note: a subject whose breathing disorder has been treated by tonsillectomy/ adenoidectomy remains eligible.
Any other diagnosed sleep-wake disorder as defined in DSM-5 or ICSD-3 (e.g., restless legs syndrome, circadian rhythm sleep wake disorder, parasomnias, narcolepsy) at Screening.
Any of the following conditions related to suicidality:
Any acute or unstable significant medical condition (e.g., seizure disorder, bipolar disorder, schizophrenia), hematology/biochemistry test results, and/or electrocardiogram results deviating from the normal ranges to a clinically relevant extent that would preclude participation in the study or could prevent the subject from complying with study requirements, as per investigator judgement.
Cognitive behavior therapy for any indication is allowed only if it has been started at least 1 month prior to Visit 2 and is kept stable throughout the study.
Clareo Health | Dose-finding Study Assessing the Efficacy, Safety, and Pharmacokinetics of Daridorexant in Subjects Aged 10 to < 18 Years With Insomnia Disorder
