A Study to Investigate the Pharmacokinetics of Midazolam After Repeated Doses of Camizestrant (AZD9833) and to Investigate the Pharmacokinetics of Camizestrant When Administered Alone and in Combination With Carbamazepine in Healthy Post-Menopausal Female Participants
- Sponsor
- AstraZeneca
- Study ID
- NCT06547164
- Phase
- PHASE1
- Status
- Completed
Conditions
- Healthy Participants
Eligibility Criteria
- Sex
- FEMALE
- Age
- 50 Years - 70 Years
- Healthy Volunteers
- Accepted
Interventions
- Midazolam — DRUGMidazolam will be administered orally.
- Camizestrant — DRUGCamizestrant will be administered orally.
- Carbamazepine — DRUGCarbamazepine will be administered orally.
Study Details
This study will be conducted in order to determine the effect of repeated oral doses of camizestrant on the pharmacokinetics (PK) of midazolam and to determine the effect of repeated oral titrated doses of carbamazepine on the PK of camizestrant in healthy post-menopausal female participants.
Key Dates
- Start date
- Aug 27, 2024
- Status verified
- Aug 2025
- Primary completion
- Aug 20, 2025
- Completion
- Aug 20, 2025
Study Design
- Enrollment
- 40 participants (actual)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- Experimental: Part B: Camizestrant + CarbamazepineParticipants will receive a single oral dose of camizestrant on Day 1 with PK sampling on Day 1 to Day 4 in Period 1, followed by low oral doses of carbamazepine BID on Day 4 to Day 6, mid oral doses of carbamazepine BID on Day 7 to Day 9 and high oral doses of carbamazepine BID on Day 10 to Day 15 with single oral dose of camizestrant on Day 13 with PK sampling on Day 16 in Period 2.
- Experimental: Part A: Midazolam + CamizestrantParticipants will receive a single oral dose of midazolam on Day 1 in Period 1, followed by oral dose of camizestrant OD from Day 2 to Day 6 in Period 2, and then single oral dose of midazolam with camizestrant on Day 7 with PK sampling on Day 7 to Day 8 in Period 3.
Primary Outcome Measure
Part A: Area under concentration-time curve from time 0 to infinity (AUCinf) of midazolam [ Time Frame: Period 1 (Day 1) and Period 3 (Day 7 to Day 8) ]
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