A Study to Measure Daridorexant in Breast Milk of Healthy... | NCT05632393

NCT05632393

Protocol Section

Identification Module

Results Section

No data available

No data is available for this block.

Annotation Section

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No data is available for this block.

Document Section

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No data is available for this block.

Derived Section

Miscellaneous Info Module

Status Module

Label	Type	Description	Intervention Names
Daridorexant 50 mg	Experimental	Daridorexant 50 mg will be administered once in the morning of Day 1.	Drug: Daridorexant

Name	Type	Description	Arm Group Labels	Other Names
Daridorexant	Drug	Daridorexant will be available as film-coated tablets for oral administration formulated at a strength of 50 mg.	Daridorexant 50 mg

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
Milk pharmacokinetic endpoints: Amount of daridorexant excreted (mg)	Cumulative amount excreted in breast milk over the collection time	0 to 72 hours after study treatment administration (Total duration: up to 4 days)

Other Outcomes

Measure	Description	Time Frame
Milk pharmacokinetic endpoints: Fraction (percentage) of dose excreted in breast milk		0 to 72 hours after study treatment administration (Total duration: up to 4 days)
Milk pharmacokinetic endpoints: Relative infant daridorexant dose (percentage)	Percentage of dose that would be consumed by the infant, adjusted to maternal weight and infant weight on Day -1

Eligibility Module

Eligibility Criteria

Inclusion Criteria:

Signed informed consent in a language understandable to the subject prior to any study-mandated procedure.
Healthy lactating female subject aged at least 18 years at Screening.
Female subject who has delivered a term infant (≥ 37 weeks' gestation) and who is breastfeeding her infant (and/or pumping) for at least 2 weeks postpartum at Screening; lactation must be well-established to maintain an adequate milk supply with regular breastfeeding (and/or pumping, e.g., 3 to 4 times per day and not providing more than 1 supplemental bottle of formula per day and the infant has not started eating solids). Subjects planning on weaning their infants after enrollment who meet the afore mentioned requirements will be considered for enrollment in the study.
Agreement to refrain from breastfeeding any infant with her own milk from Day -1 up to 72 h after study treatment administration.
Ability of subject's infant to feed from a bottle or no anticipated compromise of subject's infant's nutrition with time period of refraining from breastfeeding planned during the study.
Agreement to collect breast milk from pre-dose (directly prior to study treatment administration) to Day 4 (72 h after study treatment administration) using an electric pump provided by the study site.
Must agree to use an acceptable effective method of contraception consistently and correctly (e.g., oral progestin-only contraceptive; implants; intra uterine devices; male or female condom with or without spermicide; cap, diaphragm or sponge with spermicide) from Screening up to at least 72 h after study treatment administration, be sexually inactive, or be in same-sex relationship.

Exclusion Criteria:

Known hypersensitivity to daridorexant or treatments of the same class, or any of its excipients.
History of narcolepsy.
Mastitis or other condition that prevents the collection of breast milk from one or both breasts at Screening or on Day -1.
History of breast implants, breast augmentation, or breast reduction surgery which prevents the collection of breast milk.
Any circumstances or conditions, which, in the opinion of the investigator, may affect full participation in the study or compliance with the protocol.