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Active, not recruiting Phase 2 Interventional

A Study of LY3938577 in Participants With Type 2 Diabetes Previously Treated With Basal Insulin

ClinicalTrials.gov ID: NCT07215312

Public ClinicalTrials.gov record NCT07215312. 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 Sep 1, 2026, 10:12 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 2, Randomized, Open-Label, Comparator-Controlled Trial to Evaluate the Efficacy and Safety of LY3938577 in Study Participants, With Type 2 Diabetes Previously Treated With Basal Insulin

Brief summary

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

The purpose of this study is to see how well LY3938577 works and how safe it is compared to degludec in people with type 2 diabetes. Participation in the study will last about 26 weeks.

Study identification

NCT ID
NCT07215312
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Eli Lilly and Company
Industry
Enrollment
100 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 70 Years
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
Oct 12, 2025
Primary completion
Oct 31, 2026
Completion
Nov 30, 2026
Last update posted
Jul 12, 2026

2025 – 2026

United States locations

U.S. sites
20
U.S. states
11
U.S. cities
20
Facility City State ZIP Site status
Tucson Clinical Research Institute Tucson Arizona 85712
Encompass Clinical Research Spring Valley California 91978
University Clinical Investigators, Inc. Tustin California 92780
Tampa Bay Medical Research Clearwater Florida 33761
Encore Medical Research Hollywood Florida 33024
Clinical Research of Central Florida Lakeland Florida 33805
Encore Medical Research - Weston Weston Florida 33331
Iowa Diabetes and Endocrinology Research Center West Des Moines Iowa 50266
Washington University School of Medicine St Louis Missouri 63110
Accellacare - Wilmington Wilmington North Carolina 28401
AMR Clinical Norman Oklahoma 73069
Tribe Clinical Research, LLC Greenville South Carolina 29607
Holston Medical Group Bristol Tennessee 37620
Texas Diabetes & Endocrinology, P.A. Austin Texas 78749
Velocity Clinical Research, Dallas Dallas Texas 75230
Juno Research Houston Texas 77040
Southern Endocrinology Associates Mesquite Texas 75149
Consano Clinical Research, LLC Shavano Park Texas 78231
Texas Valley Clinical Research Weslaco Texas 78596
Chrysalis Clinical Research St. George Utah 84790

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 6 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07215312, 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 Jul 12, 2026 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07215312 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →