Study of MB-102 (Relmapirazin) and the Use of the MediBeacon® Transdermal GFR Measurement System Using the TGFR Reusable Sensor With Disposable Adhesive Ring
Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
MediBeacon
Age
18–any
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Eligible female non-pregnant participants who are either not of child-bearing potential or willing to use adequate contraception during the trial
Males must be willing to practice abstinence or utilize adequate contraception from dosing day to at least 7 days post-dose
For women of childbearing potential, the participant should have a negative serum pregnancy test at screening, and agrees to one of the following acceptable contraceptive methods used consistently and correctly i.e. abstinence, oral contraceptive either combined or progesterone alone; injectable progesterone, implants of levonorgestrel, estrogenic vaginal ring, percutaneous contraceptive patches, IUD device or system or male partner sterilization
Men will not donate sperm during the study and for 1 month following the last dose of study drug.
Participants who are capable of directly providing informed consent and who can comply with the requirements and restrictions required by the protocol
Adequate venous access sufficient to allow blood sampling per protocol requirements
You may not be if
Participants positive for COVID-19 at the time of dosing
Recent donation or loss of blood or plasma: 100 mL to 499 mL within 30 days prior to the initial dose of the study medication; or more than 499 mL within 56 days prior to the initial dose of study medication
Non-steroidal anti-inflammatory (NSAID) use within 3 days of MB-102 dosing
The participant has participated in a clinical trial and has received an investigational product within the following time ranges: prior to the first dosing day in the current study: either 30 days or 5 half-lives of the investigational product (whichever duration is longer).
History of skin sensitivity to adhesives (e.g. Band-Aids, surgical tape)
History of severe allergic hypersensitivity reactions (unacceptable adverse events) or anaphylactoid reaction to any allergen including drugs, MB-102 or other related products (intolerance to a drug is not considered a drug allergy).
Any characteristics which, in the opinion of the investigator, makes the participant a poor candidate for participation in the clinical trial
Significant scaring, tattoos or alterations in pigmentation on the sternum or other sensor location testing areas that would alter sensor readings versus other areas of the skin
Use of tanning sprays, tanning products etc. on the upper chest within 2 weeks of dosing day
Use make-up, lotions, Vaseline or other products on the area of the upper chest on the day prior to or the day of dosing
Any serious or uncontrolled medical disorder, active infection, physical exam finding, laboratory finding, or psychiatric condition that in the opinion of the investigator would limit the participant's ability to complete study requirements or may put the participant at increased risk or compromise the interpretability of study results.
Currently receiving dialysis
Currently anuric
Positive serum pregnancy test
Participants with an eGFR \> 120 mL/min/1.73m\^2
Clareo Health | Study of MB-102 (Relmapirazin) and the Use of the MediBeacon® Transdermal GFR Measurement System Using the TGFR Reusable Sensor With Disposable Adhesive Ring
