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NCT03019536 · ClinicalTrials.gov registry record · Phase 1

A Study of LY3303560 in Participants With Mild Cognitive Impairment or Alzheimer's Disease

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

Completed
Registry status
Phase 1
Development phase
22
Enrollment target

NCT03019536 is a Phase 1 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 22 participants.

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The verdict

NCT03019536, a Phase 1 study, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 1
Development phase
22 participants
Enrollment target

Study Summary

The study involves repeated doses of LY3303560 given by infusion for 49 weeks. The study will examine how safe repeated doses of LY3303560 are, whether they cause side effects in participants with mild cognitive impairment or Alzheimer's Disease, and how LY3303560 is handled by the body and acts in the body. This study will last up to 65 weeks, not including screening. Screening is required within 90 days prior to the start of the study.

Interventions

  • DRUG Flortaucipir F18
  • DRUG Florbetapir F 18
  • DRUG Placebo - IV
  • DRUG LY3303560 - IV

Trial Details

FieldValue
Enrollment Target 22 participants
Start Date 2017-01-31
Est. Completion 2019-06-05
Phase Phase 1

Sponsor

Eli Lilly and Company

1,341 total trials

What the Registry Record Tells You About NCT03019536

The ClinicalTrials.gov registry entry for NCT03019536 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 22 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Eli Lilly and Company, which has 1,341 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 4 interventions - of which Flortaucipir F18 is the first listed.

NCT03019536 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03019536 about?

NCT03019536 is a clinical study titled "A Study of LY3303560 in Participants With Mild Cognitive Impairment or Alzheimer's Disease". The study involves repeated doses of LY3303560 given by infusion for 49 weeks. The study will examine how safe repeated doses of LY3303560 are, whether they cause side effects in participants with mild cognitive impairment or Alzheimer's Disease, and how LY3303560 is handled by the body and acts in ...

What is the current status of trial NCT03019536?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 22 participants. The study started on 2017-01-31. Estimated completion is 2019-06-05.

What interventions are being tested in trial NCT03019536?

The interventions under investigation include: Flortaucipir F18 (DRUG), Florbetapir F 18 (DRUG), Placebo - IV (DRUG), LY3303560 - IV (DRUG).

Who is sponsoring clinical trial NCT03019536?

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

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.