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OpenTrials
Completed

NCT Number: NCT03136237

A Drug-Drug Interaction Study to Evaluate Drug Transporter Interactions

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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Key information

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Key Inclusion Criteria:

  • written informed consent
  • acceptable birth control measures for male subjects and women of childbearing potential
  • creatinine clearance of at least 80 mL/min by Cockcroft-Gault equation
  • complies with all required study procedures and restrictions

Key Exclusion Criteria:

  • clinically significant medical history, current medical or psychiatric condition
  • clinically significant ECG finding, vital sign measurement or laboratory/urinalysis abnormality at screening or baseline
  • current use, or use of any prescribed or over the counter medication, vitamins or herbal products within 14 days of Day 1
  • use of medication that is known to inhibit or induce metabolic enzymes or transporters within 30 days of dosing
  • participation in any other investigational drug study within 90 days of screening
  • recent or current history of alcohol or drug abuse
  • regular recent use of tobacco or nicotine products
  • positive serology for HBV, HCV, or HIV
  • pregnant or nursing
  • donation or loss of greater than 400 mL of blood within the previous 3 months
  • history of severe hypersensitivity to any medicinal product
  • for subjects enrolled in cohort 1, current use of antibiotics or probiotics, or use within 6 months prior to Day 1

Treatment and study plan

BCX7353

Drug

Day 11-18 for Cohort 1, Day 7-14 for Cohort 2, Day 1 for Cohort 3

Digoxin

Drug

Day 1 of Cohort 1

BCX7353 + digoxin

Drug

Day 19 of Cohort 1

Rosuvastatin

Drug

Day 1 of Cohort 2

rosuvastatin + BCX7353

Drug

Day 15 of Cohort 1

Cyclosporine + BCX7353

Drug

Day 14 of Cohort 3

Primary outcomes

  1. Cmax of probe substrate

    Time frame: plasma pharmacokinetic parameters are based on blood sampling over a 48 - 72 hour period

  2. AUClast of probe substrate

    Time frame: plasma pharmacokinetic parameters are based on blood sampling over a 48 - 72 hour period

  3. AUCinf of probe substrate

    Time frame: plasma pharmacokinetic parameters are based on blood sampling over a 48 - 72 hour period

Secondary outcomes

  1. adverse events

    Time frame: absolute and change from baseline through end of study, approximately 30 days

  2. laboratory analyses

    Time frame: absolute and change from baseline through end of study, approximately 30 days

  3. vital signs

    Time frame: absolute and change from baseline through end of study, approximately 30 days

  4. physical examination findings

    Time frame: absolute and change from baseline through end of study, approximately 30 days

  5. electrocardiograms

    Time frame: absolute and change from baseline throughend of study, approximately 30 days

Sponsors and collaborators

Lead sponsor

BioCryst Pharmaceuticals

Industry

Registry information

Official study title

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

Important dates

Study start
2017
Primary completion
2017
Study completion
2017
First posted
May 2, 2017
Registry last updated
Oct 26, 2017

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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