A Drug Drug Interaction (DDI) Study of Selpercatinib (LY3527723) and Rosuvastatin in Healthy Participants
Completed · Phase 1
Conditions studied: Healthy
In brief
The main purpose of this study is to determine the effect of selpercatinib on the levels of rosuvastatin in the blood stream in healthy participants. This study also evaluated the safety and tolerability of rosuvastatin when administered in combination with selpercatinib in healthy participants. This study will last up to approximately 26 days excluding screening period.
Key facts
- Study ID
- NCT05906836
- Run by
- Eli Lilly and Company
- People needed
- 28
- Starts
- 2023-07-27
- Expected to finish
- 2023-10-31
- Last updated by the study team
- 2025-09-16
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Participants who are overtly healthy as determined by medical evaluation
- Participant must be Caucasian
- Body mass index (BMI) within the range of 19.0 to 32.0 kilograms per meter squared (kg/m²)
You may not qualify if…
- Have known allergies to selpercatinib-related compounds or any components of the formulation of selpercatinib, or or rosuvastatin
- • Have a significant previous or current history or presence of cardiovascular, respiratory, renal, gastrointestinal, endocrine, hematological, or neurological disorders capable of significantly altering the absorption, metabolism, or elimination of drugs; of constituting a risk when taking the investigational product
- Have used or are intending to use over-the-counter or prescription medication, including dietary supplements and herbal medications, within 14 days prior to dosing
Where it is running
- Labcorp Clinical Research LP — Dallas, Texas, United States
Full record on ClinicalTrials.gov
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