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NCE-1 Intelligence & Market Opportunity

Quviviq

Daridorexant
Sedative / hypnotic
Oral Tablet

Insomnia treatment long depended on GABA-acting hypnotics carrying dependence and next-day impairment concerns. Quviviq (daridorexant) belongs to the newer orexin-targeting generation designed around those issues.

As a dual orexin receptor antagonist, it blocks the wake-promoting orexin signal rather than broadly sedating the central nervous system, and its half-life was selected to limit residual morning effects. The tablet is taken once nightly for insomnia marked by difficulty with sleep onset or sleep maintenance.

Quviviq is a Schedule IV controlled substance with no generic competition, competing against suvorexant, lemborexant, and inexpensive generic z-drugs. Its differentiation rests on next-day performance data, making payer step-therapy policy the principal barrier to uptake.

Approval Date
07-Jan-22
NCE-1 Date
07-Jan-26
NCE Date
07-Jan-27
Commercial snapshot

Market performance & projections

Revenue ($M)
206
CAGR (%)
38.32%
Projected sales, 2026–2032 ($M)
Analyst projection, $M per year
2026
346
2027
481
2028
629
2029
754
2030
868
2031
981
2032
1,100
Molecule profile

Details & specifications

Molecule
Daridorexant
Innovator
IDORSIA PHARMACEUTICALS LTD
Dosage Form
Oral Tablet
Strength
EQ 50 mg base, EQ 25 mg base
Therapeutic Category
Sedative / hypnotic
Usage
To treat insomnia
Good to know

Frequently asked questions

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