A Study to Investigate the Effects of Daridorexant on Nighttime Breathing in Patients With Shallow or Paused Breath During Sleep

Obstructive Sleep Apnea of Adult Clinical Trial

Official title:

A Randomized, Double-blind, Placebo-controlled, 2-way Crossover Study to Investigate the Effects of Daridorexant on Nighttime Respiratory Function and Sleep in Patients With Severe Obstructive Sleep Apnea

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05458193
• Other study ID #: ID-078-121
• Secondary ID: 2022-000098-23
• Status: Completed
• Phase: Phase 1
• Start date: August 17, 2022
• Est. completion date: February 28, 2023

Study information

• Verified date: April 2023
• Source: Idorsia Pharmaceuticals Ltd.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A study on the effects of daridorexant on nighttime respiratory function in patients with severe obstructive sleep apnea (OSA).

Description:

Each subject will participate in 2 study periods. Participants will receive 50 mg daridorexant in one period and placebo in the other period. Both periods will last from Day 1 (first administration) in the evening to Day 6 in the morning (defined as End-of-Period). The 2 periods will be separated by an in-between period of 1 to 2 weeks. An End-of-Study examination will take place 1 to 2 weeks after last administration of study treatment.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. completion date: February 28, 2023
• Est. primary completion date: February 28, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Signed informed consent in a language understandable to the participant prior to any study-mandated procedure.

• Male and female participants aged 18 years or older at Screening.

• Diagnosis of Obstructive Sleep Apnea (OSA) according to the International Classification of Sleep Disorders, documented by medical history and confirmed by a specialist.

• Severe intensity of OSA determined during OSA diagnosis and confirmed during both screening night polysomnography (PSG) and defined as apnea/hypopnea index greater than or equal to 30 events per hour.

• Patient who may require a continuous positive airway pressure (CPAP) device or a dental appliance device for the treatment of OSA must either not have started it or have withdrawn from it at least 2 months before randomization in this study. In all cases patients must not start using this type of device during the study.

• Women of childbearing potential must have a negative serum pregnancy test at Screening Visit 1 and a negative urine pregnancy test on Day 1 pre-dose of the first study period. She must agree to consistently and correctly use a highly effective method of contraception with a failure rate of less than 1% per year, be sexually inactive, or have a vasectomized partner. If a hormonal contraceptive is used, it must be initiated at least 1 month before first treatment administration.

• Woman of non-childbearing potential, i.e., postmenopausal, with previous bilateral salpingectomy, bilateral salpingo-oophorectomy or hysterectomy, or with premature ovarian failure (confirmed by a specialist), XY genotype, Turner syndrome, or uterine agenesis.

Exclusion Criteria:

• Any circumstances or conditions, which, in the opinion of the investigator, may affect full participation in the study or compliance with the protocol.

• Legal incapacity or limited legal capacity or vulnerability (e.g., kept in detention) at Screening.

• Pregnant or lactating woman.

• Modified Swiss Narcolepsy Scale total score less than 0 at Screening or history of narcolepsy or cataplexy.

• Participant with clinically significant abnormality present on either or both screening night PSG.

• Evidence of any other clinically significant active pulmonary disease such as chronic obstructive pulmonary disease (as per Global Initiative for Obstructive Lung Disease), based on investigator's judgment.

• History of surgical intervention for OSA, except nose surgery.

• Subject is the investigator or any sub investigator, research assistant, pharmacist, study coordinator, other staff from study site or the sponsor directly involved in the conduct of the study or their relatives.

Related Conditions & MeSH terms

• Obstructive Sleep Apnea of Adult
• Sleep Apnea Syndromes
• Sleep Apnea, Obstructive

Intervention

Drug:
• Daridorexant
Film-coated tablet for oral use
• Placebo
Film-coated tablet for oral use

Locations

Country	Name	City	State
Germany	ASR Advanced Sleep Research GmbH	Berlin

Sponsors (1)

Lead Sponsor	Collaborator
Idorsia Pharmaceuticals Ltd.

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Treatment difference (daridorexant - placebo) for apnea/hypopnea index	The treatment difference will be assessed at Night 5 of period 1 and period 2 after repeated-dose administration, as measured by polysomnography.; Polysomnography recording will start at the time of "lights off" and last for 8 hours.; The apnea/hypopnea index is defined by the total number of apneas (pause in respiration = 10 sec) plus hypopneas (peak signal excursions drop by = 30% of pre-event baseline for at least 10 sec accompanied by a decrease of SpO2 = 3% from pre-event baseline and/or the event is associated with an arousal) during total sleep time (TST), divided by TST (in min), then multiplied by 60.	Night 5 of period 1 and period 2 (Total duration: 2 days)
Secondary	Treatment difference (daridorexant - placebo) in mean peripheral oxygen saturation (SpO2) during total sleep time	The treatment difference will be assessed at Night 5 of period 1 and period 2 after repeated-dose administration, as measured by pulse oximetry.; Pulse oximetry recording will start at the time of "lights off" and last for 8 hours.	Night 5 of period 1 and period 2 (Total duration: 2 days)
Secondary	Treatment difference (daridorexant - placebo) for total sleep time	The treatment difference will be assessed at Night 5 of period 1 and period 2 after repeated-dose administration, as measured by polysomnography.; Polysomnography recording will start at the time of "lights off" and last for 8 hours.	Night 5 of period 1 and period 2 (Total duration: 2 days)
Secondary	Daridorexant plasma concentration		9 hours post-dose on Day 2 and Day 6 (Total duration: up to 2 days)
Secondary	Incidence of treatment-emergent adverse events	A treatment-emergent adverse event is any adverse event temporally associated with the use of a study treatment, whether or not considered related to the study treatment.	Day 1 up to Day 13 (Total duration: 13 days)