A Study of Effects of Selpercatinib (LY3527723) on Repaglinide in Healthy Participants
Completed · Phase 1
Conditions studied: Healthy
In brief
The main purpose of this study is to assess the effect of selpercatinib on how fast repaglinide gets into the blood stream and how long it takes the body to remove it when administered in healthy participants. Information about safety and tolerability will be collected. The study will last up to 12 days.
Key facts
- Study ID
- NCT05469113
- Run by
- Eli Lilly and Company
- People needed
- 16
- Starts
- 2019-01-29
- Expected to finish
- 2019-03-05
- Last updated by the study team
- 2025-12-11
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Body mass index (BMI) ≥ 18.0 and ≤ 32.0 kilograms per meter squared (kg/m²) and had a minimum weight of at least 50 kg at screening
- Have normal blood pressure, pulse rate, electrocardiogram (ECG), and blood and urine laboratory test results that are acceptable for the study
- Hemoglobin (Hb) A1c value < 6.5 % at screening and fasting glucose ≤ 126 mg/dL.
- Males who are capable of fathering a child must agree to use one of the following methods of contraception from the time of the dose administration through 6 months after the last dose
- Female of non-childbearing potential only or must have undergone sterilization procedures at least 6months prior to the first dosing
You may not qualify if…
- History or presence of diabetes or history of prior episode(s) of hypoglycemia.
- Estimated creatinine clearance <90 mL/min at Screening or Check-in (Day -1, Period 1)
- Unable to refrain from or anticipates the use of any drug, including prescription and non prescription medications, herbal remedies, or vitamin supplements for 14 days prior to the first dosing and through EOT or ET. After first dosing, acetaminophen (up to 2 g per 24 hours) may be administered at the discretion of the PI or designee
Where it is running
- Celerion — Tempe, Arizona, United States
Full record on ClinicalTrials.gov
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