Covance CRU
Leeds, LS2 9LH, United Kingdom
NCT Number: NCT03136237
This is an open-label, three part study to evaluate the effect of BCX7353 on drug transporters as well as the effect of an inhibitor of drug transport on BCX7353.
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Notify Me18 year–55 year
All sexes
Interventional
Phase 1
Leeds, LS2 9LH, United Kingdom
This is a single center, open-label, fixed-sequence, drug interaction study to evaluate the effect of BCX7353 on the pharmacokinetics of the P-gp substrate digoxin and the BCRP substrate rosuvastatin, as well as the effect of the P-gp inhibitor cyclosporine on the pharmacokinetics of BCX7353.
It is planned that 54 subjects will be enrolled into 3 cohorts of 18 subjects each. Cohort 1 will evaluate the effects of multiple doses of BCX7353 on single-dose pharmacokinetics of digoxin. Cohort 2 will evaluate the effect of multiple doses of BCX7353 on the pharmacokinetics of rosuvastatin. Cohort 3 will evaluate the effect of a single dose of cyclosporine on the pharmacokinetics of BCX7353. Cohorts may be dosed in parallel or in any order.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Key Inclusion Criteria:
Key Exclusion Criteria:
Day 11-18 for Cohort 1, Day 7-14 for Cohort 2, Day 1 for Cohort 3
Day 1 of Cohort 1
Day 19 of Cohort 1
Day 1 of Cohort 2
Day 15 of Cohort 1
Day 14 of Cohort 3
Time frame: plasma pharmacokinetic parameters are based on blood sampling over a 48 - 72 hour period
Time frame: plasma pharmacokinetic parameters are based on blood sampling over a 48 - 72 hour period
Time frame: plasma pharmacokinetic parameters are based on blood sampling over a 48 - 72 hour period
Time frame: absolute and change from baseline through end of study, approximately 30 days
Time frame: absolute and change from baseline through end of study, approximately 30 days
Time frame: absolute and change from baseline through end of study, approximately 30 days
Time frame: absolute and change from baseline through end of study, approximately 30 days
Time frame: absolute and change from baseline throughend of study, approximately 30 days
BioCryst Pharmaceuticals
Industry
A Phase 1 Study to Evaluate the Effect of BCX7353 on the Single Dose Pharmacokinetics of the P-gp Substrate Digoxin and the BCRP Substrate Rosuvastatin and the Effect of the P-gp Inhibitor Cyclosporine on the Single Dose Pharmacokinetics of BCX7353
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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