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NCT06181006 · ClinicalTrials.gov registry record · Phase 1

A Study to Evaluate Pirtobrutinib (LOXO-305) in Healthy Adult Participants

A Phase 1 study, sponsored by Eli Lilly and Company.

Completed
Registry status
Phase 1
Development phase
24
Enrollment target

NCT06181006: Completed Phase 1 study, sponsored by Eli Lilly and Company.

NCT06181006 is a Phase 1 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 24 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (60% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06181006, a Phase 1 study, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 1
Development phase
24 participants
Enrollment target

Study Summary

The main purpose of this study is to assess the safety and tolerability of pirtobrutinib and to look at the amount of the study drug, pirtobrutinib, that gets into the blood stream and how long it takes the body to get rid of it when given in healthy adult participants. For each participant, the total duration of the study will be 46 days, including screening.

Primary Outcome

TEAE is defined as an adverse event (AE) which starts on or after the first administration of study drug. A serious adverse event is defined as any AE occurring at any dose that results in any of the following outcomes: death; a life-threatening adverse drug experience; inpatient hospitalization or prolongation of existing hospitalization; a persistent or significant disability/incapacity; a congenital anomaly/birth defect; an important medical event that may require medical or surgical interven

Interventions

  • DRUG Pirtobrutinib

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2020-08-14
Est. Completion 2020-12-01
Phase Phase 1
Eli Lilly and Company

1,341 total trials

What the finished NCT06181006 record still lists

NCT06181006 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (60% lower).

The record links to 0 conditions, and to 1 intervention - of which Pirtobrutinib is the first listed.

NCT06181006 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06181006 about?

NCT06181006 is a clinical study titled "A Study to Evaluate Pirtobrutinib (LOXO-305) in Healthy Adult Participants". The main purpose of this study is to assess the safety and tolerability of pirtobrutinib and to look at the amount of the study drug, pirtobrutinib, that gets into the blood stream and how long it takes the body to get rid of it when given in healthy adult participants. For each participant, the tot...

What is the current status of trial NCT06181006?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 24 participants. The study started on 2020-08-14. Estimated completion is 2020-12-01.

What interventions are being tested in trial NCT06181006?

The interventions under investigation include: Pirtobrutinib (DRUG).

Who is sponsoring clinical trial NCT06181006?

This trial is sponsored by Eli Lilly and Company, which has 1,341 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06181006's enrollment target sits among peer trials

24 1520th of 2000 higher than 405 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06181006, the US trial registry maintained by the National Library of Medicine. NCT06181006 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.