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NCT01299285 · ClinicalTrials.gov registry record · Phase 1

Disposition of 14C-LY3009104 Following Oral Administration in Healthy Human Subjects

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

Completed
Registry status
Phase 1
Development phase
6
Enrollment target

NCT01299285: Completed Phase 1 study, sponsored by Eli Lilly and Company.

NCT01299285 is a Phase 1 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 6 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01299285, a Phase 1 study, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 1
Development phase
6 participants
Enrollment target

Study Summary

This is a single dose study of radiolabeled \[14C\]-LY3009104 in healthy male volunteers to study the absorption, distribution, metabolism, and elimination of LY3009104. This study requires minimum of 7 days and maximum of 22 days stay. This study is for research purposes only and is not intended to treat any medical condition.

Interventions

  • DRUG LY3009104

Trial Details

FieldValue
Enrollment Target 6 participants
Start Date 2011-02
Est. Completion 2011-03
Phase Phase 1
Eli Lilly and Company

1,341 total trials

What the finished NCT01299285 record still lists

NCT01299285 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 6 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (90% lower).

The record links to 0 conditions, and to 1 intervention - of which LY3009104 is the first listed.

NCT01299285 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01299285 about?

NCT01299285 is a clinical study titled "Disposition of 14C-LY3009104 Following Oral Administration in Healthy Human Subjects". This is a single dose study of radiolabeled \[14C\]-LY3009104 in healthy male volunteers to study the absorption, distribution, metabolism, and elimination of LY3009104. This study requires minimum of 7 days and maximum of 22 days stay. This study is for research purposes only and is not intended to...

What is the current status of trial NCT01299285?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 6 participants. The study started on 2011-02. Estimated completion is 2011-03.

What interventions are being tested in trial NCT01299285?

The interventions under investigation include: LY3009104 (DRUG).

Who is sponsoring clinical trial NCT01299285?

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 NCT01299285's enrollment target sits among peer trials

6 1974th of 2000 higher than 12 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 NCT01299285, the US trial registry maintained by the National Library of Medicine. NCT01299285 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.