Covance Clinical Research Unit, Inc.
Dallas, Texas, 75247, United States
NCT Number: NCT04800614
An Open-label, Randomized, Three-period, Crossover Study of the Effect of Food on the Pharmacokinetics of a Single Oral Dose of Sitravatinib in Healthy Adult Subjects
Looking for future studies?
Notify Me18 year–55 year
All sexes
Interventional
Phase 1
Dallas, Texas, 75247, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Key Inclusion Criteria:
Key Exclusion Criteria:
100 mg sitravatinib on Day 1 of each of 3 periods
Time frame: Up to 72 hours after dosing
Maximum observed plasma concentration
Time frame: Up to 72 hours after dosing
Area under the plasma concentration-time curve from time zero extrapolated to infinity
Time frame: Up to 72 hours after dosing
AUC from time zero to the last measured time point
Time frame: Up to 44 days
Incidence and severity of adverse events (AEs) dosed in the fasted and fed states in healthy adult subjects
Looking for future studies?
Notify MeMirati Therapeutics Inc.
Industry
An Open-label, Randomized, Three-period, Crossover Study of the Effect of Food on the Pharmacokinetics of a Single Oral Dose of Sitravatinib in Healthy Adult Subjects
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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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