A Study to Assess the Effect of Single Doses of Daridorexant on Electrocardiogram Parameters in Healthy Subjects

Phase 1

Completed

• Conditions: Healthy
• Interventions: Drug: Placebo; Drug: Moxifloxacin; Drug: Daridorexant

• Registration Number: NCT04250506
• Lead Sponsor: Idorsia Pharmaceuticals Ltd.

Brief Summary

A study to assess the effect of single doses of daridorexant on electrocardiogram parameters in healthy subjects

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2020-01-30
• Study First Submitted QC: 2020-01-30
• Study First Posted: 2020-01-31
• Study Start: 2020-02-28
• Primary Completion: 2020-07-22
• Study Completion: 2020-07-22
• Status Verified: 2020-09
• Last Update Submitted: 2020-09-15
• Last Update Posted: 2020-09-16

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 36

Inclusion Criteria

• Signed informed consent in the local language prior to any study-mandated procedure.

• Czech citizen with the ability to communicate well with the investigator, in a language understandable to the subject, and to understand and comply with the requirements of the study.

• Healthy male and female subjects aged 18 to 55 years (inclusive) at Screening.

• 12-lead safety ECG: QTcF < 450 ms for male subjects and < 470 ms for female subjects, QRS < 110 ms, and PR < 220 ms, and resting HR > 50 bpm and < 90 bpm with no clinically relevant abnormalities on 12-lead ECG after 5 min in the supine position at Screening and on Day 1 pre-dose of Period 1.

• Healthy on the basis of medical history, physical examination, cardiovascular assessments, and clinical laboratory tests.

• Women of childbearing potential are eligible only if the following applies:

  1. Negative serum pregnancy test at Screening.
  2. Negative serum pregnancy test on Day 1 of the first period.
  3. Agreement to consistently and correctly use a highly effective method of contraception with a failure rate of < 1% per year, be sexually inactive, or have a vasectomized partner from Screening up to at least 30 days after last study treatment administration in the last period with wash-out periods included. If a hormonal contraceptive is used, it must be initiated at least 1 month before first treatment administration.

• Women of non-childbearing potential must meet at least one of the following criteria:

  1. Previous bilateral salpingectomy, salpingo-oophorectomy, or hysterectomy.
  2. Premature ovarian failure confirmed by a specialist gynecologist.
  3. Post-menopausal, defined as 12 consecutive months with amenorrhea prior to Screening without alternative medical cause and confirmed with follicle-stimulating hormone (FSH) test.
  4. XY genotype.
  5. Turner syndrome.
  6. Uterine agenesis.

Exclusion Criteria

• Pregnant or lactating women.
• Previous exposure to daridorexant.
• Known hypersensitivity to moxifloxacin or any of the drug product excipients or to other fluoroquinolone antibiotics.
• Any contraindication to moxifloxacin treatment.
• History of major medical or surgical disorders which, in the opinion of the investigator, are likely to interfere with the absorption, distribution, metabolism, or excretion of the study treatments (appendectomy and herniotomy allowed, cholecystectomy not allowed).
• Any circumstances or conditions, which, in the opinion of the investigator, may affect full participation in the study or compliance with the protocol.
• History or presence of rhythm disorders (e.g., sinoatrial heart block, sick-sinus syndrome, second- or third-degree atrioventricular block, long QT syndrome, symptomatic bradycardia, atrial flutter, or atrial fibrillation) or electrolyte disturbances, particularly hypokalemia.
• Any sleep-disorder including self-reported insomnia disorder, breathing-related sleep disorders, restless legs syndrome, nightmare disorder, non-rapid eye movement sleep arousal disorders (sleep terror disorder or sleepwalking disorder), rapid eye movement sleep behavior disorder, circadian rhythm sleep-wake disorders.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
Treatment C: Placebo	Placebo	Placebo administered as tablets (4 x 50 mg) for oral use.
Treatment D: Moxifloxacin 400 mg	Moxifloxacin	Moxifloxacin administered as film-coated tablets for oral use.
Treatment A: Daridorexant 50 mg	Daridorexant	Daridorexant (ACT-541468) administered as film-coated tablets for oral use.
Treatment B: Daridorexant 200 mg	Daridorexant	Daridorexant (ACT-541468) administered as film-coated tablets (4 x 50 mg) for oral use.

Primary Outcome Measures

Name	Time	Method
Placebo-corrected change from baseline in the HR-corrected QTcF (ΔΔQTcF)	Various time points (for up to 24 hours) on Day 1 and Day 2 of each period. The 4 periods will be separated by a wash-out period of 7-10 days. Total duration: up to 8 weeks.

Secondary Outcome Measures

Name	Time	Method
Plasma PK parameters of daridorexant: - AUC from 0 to 24 hours (AUC0-24)	Various time points (for up to 24 hours) on Day 1 and Day 2 of each period. The 4 periods will be separated by a wash-out period of 7-10 days. Total duration: up to 8 weeks.
Plasma PK parameters of daridorexant: - T½	Various time points (for up to 24 hours) on Day 1 and Day 2 of each period. The 4 periods will be separated by a wash-out period of 7-10 days. Total duration: up to 8 weeks.
Plasma PK parameters of daridorexant: - Maximum plasma concentration (Cmax)	Various time points (for up to 24 hours) on Day 1 and Day 2 of each period. The 4 periods will be separated by a wash-out period of 7-10 days. Total duration: up to 8 weeks.
Plasma PK parameters of daridorexant: - Time to reach Cmax (tmax)	Various time points (for up to 24 hours) on Day 1 and Day 2 of each period. The 4 periods will be separated by a wash-out period of 7-10 days. Total duration: up to 8 weeks.

Trial Locations

Locations (1)

CEPHA s.r.o.; 🇨🇿 Pilsen, Czechia