Finding studies
Finding studies
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Lead
Pfizer
This is a Phase 1, open-label, randomized, 4-period, 6-sequence crossover study in healthy adult participants. The goal of this clinical study is to compare how much of the oral (taken by mouth) study drug ibuzatrelvir is in participants' blood after taking one of the two different types of tablets containing the same amount of ibuzatrelvir without food (fasted). The study will also measure how much ibuzatrelvir is in participants' blood after taking one type of the tablets dispersed in water and when one type of the tablets is taken with food. Safety and tolerability after taking the study medication will also be assessed. Healthy adult participants will be screened within 28 days prior to the first day of study treatment. Participants will take one dose of study drug on the first day of each of 4 dosing periods that are 2-3 days each. Participants will remain in the clinical research unit (CRU) from Day -1 of Period 1 until completion of procedures on Day 3 of Period 4. This means that participants will stay in the CRU for a total of 9 nights and 10 days. The follow-up phone call will take place approximately 28-35 days after the last dose of study drug. The total time in the study is about 10-11 weeks. The study treatments are: Treatment A: ibuzatrelvir (original) fasted Treatment B: ibuzatrelvir (new) fasted Treatment C: ibuzatrelvir (new as dispersion in water) fasted Treatment D: ibuzatrelvir (new) fed This is a crossover study which means that the treatment groups will receive the same treatments (A, B, C, and D) in a different order during the 4 dosing periods. Group Period 1 Period 2 Period 3 Period 4 1. A (fasted) B (fasted) C (fasted) D (Fed) 2. A (fasted) C (fasted) B (fasted) D (Fed) 3. B (fasted) A (fasted) C (fasted) D (Fed) 4. B (fasted) C (fasted) A (fasted) D (Fed) 5. C (fasted) A (fasted) B (fasted) D (Fed) 6. C (fasted) B (fasted) A (fasted) D (Fed) During the screening and time in the CRU participants will have: * Blood and urine samples collected for safety lab tests * Pharmacokinetics (PK) blood samples collected to detect concentrations of ibuzatrelvir (up to 40 samples) * Up to 8 electrocardiograms (ECGs - records the electrical signals controlling your heart) * To fast (not eat) for at least 10 hours overnight before 3 of the 4 doses Approximately 18 participants will be enrolled in the study.
Age
18–any
Sex
ALL
Healthy volunteers
Accepted
