Overview

A Drug Drug Interaction (DDI) Study of Selpercatinib (LY3527723) and Rosuvastatin in Healthy Participants

Status:
Not yet recruiting
Trial end date:
2023-10-10
Target enrollment:
0
Participant gender:
All
Summary
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 will also evaluate 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.
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Eli Lilly and Company
Treatments:
Rosuvastatin Calcium
Criteria
Inclusion Criteria:

- 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)

Exclusion Criteria:

- 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