CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 16 enrolled
Drug / intervention
Pirtobrutinib +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06194214
NCT06194214Phase 1Completed

A Phase I, Open-label, Fixed-sequence, Drug Interaction Study to Investigate the Effect of Single and Multiple Oral Doses of LOXO-305 on the Pharmacokinetics of Multiple Oral Doses of Digoxin (P-Glycoprotein Substrate) in Healthy Subjects

Eli Lilly and Company·interventional·Posted Jan 8, 2024·Updated Feb 21, 2025

In Brief

A Phase 1 clinical trial evaluating Pirtobrutinib and Digoxin for Healthy. Completed, enrolled 16 participants across 1 site.

Detailed Summary

The main purpose of this study is to evaluate the effect of Pirtobrutinib (LOXO-305) on multiple oral doses of digoxin (P-gp substrate) when administered as single and multiple doses by collecting the blood samples and conducting the blood tests to measure how much digoxin is in the bloodstream and how the body handles and eliminates it in healthy participants. The study will also evaluate the safety and tolerability of Pirtobrutinib. Participants will stay in this study for up to 58 days, including screening.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHealthy
CountriesUnited States
CollaboratorsLoxo Oncology, Inc.

Timeline

Phase 1CompletedFinished
20222023202420252026
First PostedJan 8, 2024
Enrollment StartMar 11, 2021
Primary CompletionJun 9, 2021
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 2.5 years ago

Interventions

Pirtobrutinibdrug

Administered Orally.

Digoxindrug

Administered Orally.