Discover QUVIVIQ™▼ (daridorexant), as a treatment option for adult patients with chronic insomnia1,2

- NICE recommended for primary care in chronic insomnia3
- SMC accepted for restricted use within NHSScotland4
QUVIVIQ™ (daridorexant) is indicated for the treatment of adult patients with insomnia characterised by symptoms present for at least 3 months and considerable impact on daytime functioning.1
Chronic Insomnia Topics
Diagnosing Chronic Insomnia
Browse Chronic Insomnia Patient Profiles
Discover the Different Chronic Insomnia Patient Profiles
- Explore Patient Profiles
NICE recommends Daridorexant for treating long-term insomnia
Read the evidence-based recommendations on Daridorexant (QUVIVIQ™) for treating long-term insomnia in adults.
Read the evidence-based recommendations on Daridorexant (QUVIVIQ™) for treating long-term insomnia in adults.
- Read NICE Recommendations
Understanding Chronic Insomnia
Deepen Your Understanding of Chronic Insomnia
Explore a self-led course on chronic insomnia through interactive modules and case studies.
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Practical Resources

Discuss key domains to uncover your patients’ insomnia
- Download the Resource
Patient support material from Idorsia Pharmaceuticals UK Ltd.

Summary of the two Phase 3 studies on daridorexant
- Read the Summary
Promotional material from Idorsia Pharmaceuticals UK Ltd.

Overactive wake signalling as a cause of chronic insomnia
- Watch the Video
Promotional material from Idorsia Pharmaceuticals UK Ltd.
References
- QUVIVIQ™ Idorsia Pharmaceuticals LTD, Summary of Product Characteristics.
- Mignot E, et al. Lancet Neurol. 2022. 21(2); 125–139.
- NICE. TA922. Daridorexant for treating long-term insomnia, October 2023. Available at: https://www.nice.org.uk/guidance/ta922. Last accessed July 2024.
- SMC. SMC2611. Daridorexant film-coated tablets (Quviviq®). Available at: https://www.scottishmedicines.org.uk/media/8230/daridorexant-quviviq-final-march-2024-for-website.pdf. Last accessed April 2024
This information is intended for UK healthcare professionals.
Adverse events must be reported. Healthcare professionals are asked to report any suspected adverse reactions via http://www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in Google play or Apple App store. Adverse events should also be reported to ds.safety.uk@idorsia.com.
UK-DA-00400 | Date of preparation: August 2024