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Completed Phase 3 Interventional Results available

A Study of Insulin Efsitora Alfa (LY3209590) as a Weekly Basal Insulin Compared to Insulin Glargine in Adult Participants With Type 2 Diabetes on Multiple Daily Injections

ClinicalTrials.gov ID: NCT05462756

Public ClinicalTrials.gov record NCT05462756. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 17, 2026, 12:20 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, Parallel-Design, Open-Label, Randomized Controlled Study to Evaluate the Efficacy and Safety of LY3209590 as a Weekly Basal Insulin Compared to Insulin Glargine in Adults With Type 2 Diabetes on Multiple Daily Injections

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The reason for this study is to evaluate if the once-weekly study drug insulin efsitora alfa (LY3209590) is safe and effective compared with daily insulin glargine in participants with Type 2 diabetes (T2D) that have already been treated with basal insulin and at least 2 injections per day of prandial insulin. The study consists of a 3-week screening/lead-in period, a 26-week treatment period and a 5-week safety follow-up period. The study will last up to 34 weeks.

Study identification

NCT ID
NCT05462756
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Eli Lilly and Company
Industry
Enrollment
730 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 11, 2022 (Actual)
Primary completion
Feb 27, 2024 (Actual)
Completion
Feb 27, 2024 (Actual)
Last update posted
Apr 27, 2025

2022 – 2024

United States locations

U.S. sites
24
U.S. states
13
U.S. cities
22
Facility City State ZIP Site status
CMR of Greater New Haven, LLC Hamden Connecticut 06517 —
Tampa Bay Medical Research Clearwater Florida 33761 —
Panax Clinical Research Miami Lakes Florida 33014 —
Encore Medical Research - Weston Weston Florida 33331 —
Elite Clinical Trials Blackfoot Idaho 83221 —
Rocky Mountain Clinical Research Idaho Falls Idaho 83404 —
MedStar Good Samaritan Hospital Baltimore Maryland 21239 —
NECCR PrimaCare Research Fall River Massachusetts 02721 —
Arcturus Healthcare , PLC, Troy Internal Medicine Research Division Troy Michigan 48098 —
Palm Research Center Tenaya Las Vegas Nevada 89128 —
Palm Research Center Sunset Las Vegas Nevada 89148 —
Research Foundation of SUNY - University of Buffalo Buffalo New York 14221 —
Remington Davis Clinical Research Columbus Ohio 43215 —
Aventiv Research Dublin Ohio 43016 —
Heritage Valley Multispecialty Group, Inc Beaver Pennsylvania 15009 —
Thomas Jefferson University Hospital Philadelphia Pennsylvania 19107 —
Texas Diabetes & Endocrinology, P.A. Austin Texas 78731 —
Texas Diabetes & Endocrinology, P.A. Austin Texas 78749 —
North Texas Endocrine Center Dallas Texas 75231 —
Biopharma Informatic, LLC Houston Texas 77043 —
Research Institute of Dallas Plano Texas 75093 —
Consano Clinical Research, LLC Shavano Park Texas 78231 —
Chrysalis Clinical Research St. George Utah 84790 —
Rainier Clinical Research Center Renton Washington 98057 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 57 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05462756, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 27, 2025 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05462756 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →