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NCT04476108 · ClinicalTrials.gov registry record · Phase 2

Chronic Pain Master Protocol (CPMP): A Study of LY3016859 in Participants With Diabetic Peripheral Neuropathic Pain

A Phase 2 study, sponsored by Eli Lilly and Company.

Completed
Registry status
Phase 2
Development phase
125
Enrollment target

NCT04476108: Completed Phase 2 study, sponsored by Eli Lilly and Company.

NCT04476108 is a Phase 2 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 125 participants, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04476108, a Phase 2 study, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 2
Development phase
125 participants
Enrollment target

Study Summary

This study is being done to test the safety and efficacy of the study drug LY3016859 for the treatment of diabetic peripheral neuropathic pain. This trial is part of the chronic pain master protocol H0P-MC-CPMP (NCT05986292) which is a protocol to accelerate the development of new treatments for chronic pain.

Primary Outcome

The NRS was used during the preliminary data entry period and daily throughout the study to describe pain severity. Participants were asked to describe their average pain over the past 24 hours, on a scale of 0 to 10: 0 = no pain, and 10 = pain as bad as you can imagine. Posterior mean change from baseline, 95% credible interval (CrI) was derived using Bayesian mixed model repeated measures.

Interventions

  • DRUG Placebo
  • DRUG LY3016859

Trial Details

FieldValue
Enrollment Target 125 participants
Start Date 2020-07-15
Est. Completion 2021-11-11
Phase Phase 2
Eli Lilly and Company

1,341 total trials

What the finished NCT04476108 record still lists

NCT04476108 is an interventional study that assigns participants to a tested intervention. The registered 125 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target.

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT04476108 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04476108 about?

NCT04476108 is a clinical study titled "Chronic Pain Master Protocol (CPMP): A Study of LY3016859 in Participants With Diabetic Peripheral Neuropathic Pain". This study is being done to test the safety and efficacy of the study drug LY3016859 for the treatment of diabetic peripheral neuropathic pain. This trial is part of the chronic pain master protocol H0P-MC-CPMP (NCT05986292) which is a protocol to accelerate the development of new treatments for chr...

What is the current status of trial NCT04476108?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 125 participants. The study started on 2020-07-15. Estimated completion is 2021-11-11.

What interventions are being tested in trial NCT04476108?

The interventions under investigation include: Placebo (DRUG), LY3016859 (DRUG).

Who is sponsoring clinical trial NCT04476108?

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 NCT04476108's enrollment target sits among peer trials

125 558th of 2000 higher than 1,437 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT04476108, the US trial registry maintained by the National Library of Medicine. NCT04476108 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.