About this trial
The study investigators are interested in learning more about how drugs, that are given to children by their health care provider, act in the bodies of children and young adults in hopes to find the most safe and effective dose for children. The primary objective of this study is to evaluate the PK of understudied drugs currently being administered to children per SOC as prescribed by their treating provider.
Eligibility criteria
Qualifiers
Participant is < 21 years of age
(a) Participant is receiving one or more of the study drugs of interest at the time of enrollment or (b) Participant is NOT receiving one or more of the study drugs of interest but is SARS-COV-2 positive within 60 days prior to enrollment
Disqualifiers
Participant has a known pregnancy
Has had intermittent dialysis within previous 24 hours
Has had a kidney transplant within previous 30 days
Has had a liver transplant within previous 1 year
Trial design
Treatments tested in this trial
- The POP02 study is collecting bodily fluid samples (i.e., whole blood, effluent samples) of children prescribed the following drugs of interest per standard of care:
Treatment groups
Sponsors and collaborators
Duke University
Lead sponsor
The Emmes Company, LLC
Collaborator
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Collaborator