PF-06651600
Drug200 mg by mouth (PO) Once daily (QD) for 11 days
NCT Number: NCT03608241
This is a Phase 1, randomized, 2 way crossover, multiple dose, open label study of the effect of multiple dose PF-06651600 on single dose OC PK in healthy female subjects. Subjects will be randomized to 1 of 2 treatment sequences.
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Notify Me18 year–55 year
Female
Interventional
Phase 1
Quotient Sciences, Coral Gables, Florida, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Subjects must meet all of the following inclusion criteria to be eligible for enrollment in the study:
Female subjects of non childbearing potential must meet at least 1 of the following criteria:
Exclusion criteria
Subjects with any of the following characteristics/conditions will not be included in the study:
200 mg by mouth (PO) Once daily (QD) for 11 days
Single dose of Oral tablet containing 30 ug EE and 150 ug of LN
Other names: Oral contraceptive
Time frame: 0 (pre-dose),1, 1.5. 2,4,6,8,12,24 and 48 hours post-dose
AUCinf = Area under the plasma concentration versus time curve (AUC) from time zero (pre-dose) to extrapolated infinite time (0-inf). It is obtained from AUC (0-t) plus AUC (t-inf).
Time frame: 0 (pre-dose), 1, 1.5, 2, 4, 6, 8, 12, 24 and 48 hours post-dose
AUCinf = Area under the plasma concentration versus time curve (AUC) from time zero (pre-dose) to extrapolated infinite time (0-inf). It is obtained from AUC (0-t) plus AUC (t-inf).
Time frame: Baseline (Day 0) up to 28 days after last dose of study drug
Time frame: Baseline up to 28 days after last dose
Time frame: Baseline through study completion, approximately 23 days.
Time frame: Baseline through study completion, approximately 23 days.
Pfizer
Industry
A PHASE 1, RANDOMIZED, OPEN LABEL, 2-WAY CROSSOVER STUDY TO ESTIMATE THE EFFECT OF MULTIPLE DOSE PF-06651600 ON THE PHARMACOKINETICS OF SINGLE DOSE ORAL CONTRACEPTIVE STEROIDS IN HEALTHY FEMALE SUBJECTS
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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