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NCT04230122 · ClinicalTrials.gov registry record · Phase 1

A Study of LY3478006 in Healthy Participants

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

Terminated
Registry status
Phase 1
Development phase
4
Enrollment target

NCT04230122: Clinical Trial Phase 1 study, sponsored by Eli Lilly and Company.

NCT04230122 is a Phase 1 study that was terminated before completion, run by Eli Lilly and Company. The registered enrollment target is 4 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (93% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04230122, a Phase 1 study, was terminated before completion, sponsored by Eli Lilly and Company.

TERMINATED
Registry status
Phase 1
Development phase
4 participants
Enrollment target

Study Summary

The purpose of this study is to learn more about how safe and how well tolerated LY3478006 is when given by injection into a vein or just under the skin to healthy participants. Blood tests will be done to check how much LY3478006 is in the bloodstream and how long the body takes to get rid of it. For each participant, the study will last up to about 16 weeks, including screening.

Primary Outcome

Data presented are the number of participants who experienced SAEs considered by the investigator to be related to study drug administration. A summary of SAEs and all other non-serious Adverse Event(s) (AEs), regardless of causality, is located in the Reported Adverse Event module.

Interventions

  • DRUG Placebo - IV
  • DRUG Placebo - SC
  • DRUG LY3478006 - IV
  • DRUG LY3478006 - SC

Trial Details

FieldValue
Enrollment Target 4 participants
Start Date 2020-02-17
Est. Completion 2020-06-04
Phase Phase 1
Eli Lilly and Company

1,341 total trials

Why NCT04230122 stopped before completion

NCT04230122 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 4 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (93% lower).

The record links to 0 conditions, and to 4 interventions - of which Placebo - IV is the first listed.

NCT04230122 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04230122 about?

NCT04230122 is a clinical study titled "A Study of LY3478006 in Healthy Participants". The purpose of this study is to learn more about how safe and how well tolerated LY3478006 is when given by injection into a vein or just under the skin to healthy participants. Blood tests will be done to check how much LY3478006 is in the bloodstream and how long the body takes to get rid of it. F...

What is the current status of trial NCT04230122?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 4 participants. The study started on 2020-02-17. Estimated completion is 2020-06-04.

What interventions are being tested in trial NCT04230122?

The interventions under investigation include: Placebo - IV (DRUG), Placebo - SC (DRUG), LY3478006 - IV (DRUG), LY3478006 - SC (DRUG).

Who is sponsoring clinical trial NCT04230122?

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 NCT04230122's enrollment target sits among peer trials

4 1995th of 2000 higher than 2 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 NCT04230122, the US trial registry maintained by the National Library of Medicine. NCT04230122 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.