Summary

Eligibility
for people ages 18-64 (full criteria)
Healthy Volunteers
healthy people welcome
Location
at San Francisco, California
Dates
study started
estimated completion
Principal Investigator
by Kathleen M Giacomini

Description

Summary

This is a randomized, two-arm crossover study. Subjects will undergo a placebo and rosuvastatin phase and eltrombopag and rosuvastatin phase to identify biomarkers for Breast Cancer Resistance Protein (BCRP).

Official Title

Identification and Validation of Biomarkers for Breast Cancer Resistance Protein

Details

Membrane transporters are critical in the absorption, distribution and elimination of drugs, and are important target sites for drug-drug interactions (DDIs). During drug development, clinical studies characterizing transporter-mediated DDIs are frequently required. There has been enormous interest in identifying and validating serum biomarkers or surrogate probes to be used in predicting in vivo (clinical) DDIs. These biomarkers could complement in vitro studies, reducing false positive and false negative predictions, as well as the cost and time required for clinical development.

In this randomized, two-arm crossover study, subjects will undergo a placebo and rosuvastatin phase and eltrombopag and rosuvastatin phase to identify biomarkers for a membrane transporter known as Breast Cancer Resistance Protein (BCRP). The primary goal of this study is to validate and discover BCRP candidate biomarkers in a focused clinical DDI study with healthy volunteers to determine whether they can serve as clinical biomarkers for BCRP-mediated DDIs.

Keywords

Healthy Volunteers membrane transporter drug-drug interaction rosuvastatin eltrombopag biomarker Rosuvastatin Calcium Rosuvastatin (Inhibitor arm) Eltrombopag and Rosuvastatin

Eligibility

You can join if…

Open to people ages 18-64

  • Healthy as judged by medical examination, medical history and normal biochemical and hematological measures.
  • Normal urinalysis and renal function
  • Male subjects weighing ≥ 50 kg and female subjects weighing ≥ 45 kg.
  • Understand the nature and purpose of the study and provide informed consent.

You CAN'T join if...

  • Subjects who are pregnant, breastfeeding, or unwilling to practice non-hormonal forms of birth control during participation in the study.
  • Self-reported drug allergies to rosuvastatin or eltrombopag
  • Subjects that have smoked cigarettes, have smoked or ingested THC/marijuana or have used illegal substances (i.e., opiates, cocaine) in the past year.
  • Subjects with any disease affecting or impairing the function of the liver, kidney or heart.
  • Subjects with any blood or coagulation disorders.
  • Subjects with diabetes mellitus, hyperthyroidism, hypothyroidism, cardiovascular disease, glaucoma.
  • Subjects with gastrointestinal disease, gastrointestinal disorder, or gastrointestinal surgery.
  • Subjects with known infection with HIV, Hepatitis B (HBsAg) or Hepatitis C (no laboratory diagnostics concerning these diseases will be performed within the present study).
  • Subjects that are taking prescription (i.e., birth control pills), non-prescription and dietary supplements (i.e., turmeric, quercetin, kaempferol, Gingko biloba) within seven days of receiving the study dose in each phase of the study.
  • Subjects with a condition, disease, or abnormality that in the opinion of the Investigator would compromise the safety of the patient or the quality of the data.
  • Female subjects undergoing treatment for infertility or hormone replacement therapy.
  • Subjects with abnormal laboratory results at screening as judged by the investigator or study physician.
  • Participating in another research study while participating in this research study.
  • Subjects that ingest grapefruit, grapefruit juice or grapefruit extract within seven days of receiving the study dose in each phase of the study.
  • Non-English speaking.
  • Subject has any signs or symptoms that are consistent with COVID-19. Per current CDC recommendations this includes subjects with the symptoms cough or shortness of breath or difficulty breathing, or at least two of the following symptoms: fever, chills, repeated shaking with chills, muscle pain, headache, sore throat or new loss of taste/smell. In addition, the subject has any other findings suggestive of COVID-19 risk in the opinion of the investigator.
  • Subject tests positive for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by a molecular diagnostic test (i.e., COVID19 RNA test) performed during the screening visit.

Location

  • Ucsf Ctsi Crc
    San Francisco California 94143 United States

Lead Scientist at UCSF

Details

Status
not yet accepting patients
Start Date
Completion Date
(estimated)
Sponsor
University of California, San Francisco
ID
NCT04542382
Phase
Phase 1
Study Type
Interventional
Last Updated