Actively Recruiting

Phase 2
Age: 18Years - 70Years
All Genders
ID07215312

A Phase 2 Randomized Open-Label Trial Evaluating LY3938577 Compared to Degludec in Adults With Type 2 Diabetes Previously Treated With Basal Insulin

Led by Eli Lilly and Company · Updated on 2026-05-22

100

Participants Needed

26

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the effectiveness and safety of LY3938577 compared to degludec in people with type 2 diabetes who have been previously treated with basal insulin. This Phase 2 trial aims to understand how well LY3938577 works in managing blood sugar levels in this patient population. The study is sponsored by Eli Lilly and Company and participation lasts about 26 weeks. Participants are randomly assigned to receive either LY3938577 or degludec, both given by subcutaneous injection. The study compares these two treatments to observe differences in glucose control and safety. The trial design is open-label, meaning both participants and researchers know which treatment is given. Throughout the study, researchers will monitor changes in blood sugar levels, specifically the time glucose remains in the target range of 70 to 180 mg/dL from baseline to week 20. Other measures include changes in hemoglobin A1c and drug concentration levels. Safety and treatment effects are assessed at regular intervals during the 26-week participation period.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Have type 2 diabetes
  • Are receiving at least 20 units and no more than 55 units of basal insulin per day at screening
  • Have hemoglobin A1c (HbA1c) between 7.5% and 10.5% inclusive
  • Have a body mass index (BMI) of 20 or higher and less than 35 kg/m2
Not Eligible

You will not qualify if you...

  • Have type 1 diabetes

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

Duration - 20 weeks

Participants receive either LY3938577 or degludec via subcutaneous injection as part of the study treatment.

Regular visits during treatment period

Trial Site Locations

Total: 26 locations

1

Tucson Clinical Research Institute

Tucson, Arizona, United States, 85712

Active, Not Recruiting

2

Encompass Clinical Research

Spring Valley, California, United States, 91978

Active, Not Recruiting

3

University Clinical Investigators, Inc.

Tustin, California, United States, 92780

Actively Recruiting

4

Tampa Bay Medical Research

Clearwater, Florida, United States, 33761

Actively Recruiting

5

Encore Medical Research

Hollywood, Florida, United States, 33024

Active, Not Recruiting

6

Clinical Research of Central Florida

Lakeland, Florida, United States, 33805

Completed

7

Encore Medical Research - Weston

Weston, Florida, United States, 33331

Actively Recruiting

8

Iowa Diabetes and Endocrinology Research Center

West Des Moines, Iowa, United States, 50266

Active, Not Recruiting

9

Washington University School of Medicine

St Louis, Missouri, United States, 63110

Completed

10

Accellacare - Wilmington

Wilmington, North Carolina, United States, 28401

Actively Recruiting

11

AMR Clinical

Norman, Oklahoma, United States, 73069

Completed

12

Tribe Clinical Research, LLC

Greenville, South Carolina, United States, 29607

Completed

13

Holston Medical Group

Bristol, Tennessee, United States, 37620

Actively Recruiting

14

Texas Diabetes & Endocrinology, P.A.

Austin, Texas, United States, 78749

Active, Not Recruiting

15

Velocity Clinical Research, Dallas

Dallas, Texas, United States, 75230

Active, Not Recruiting

16

Juno Research

Houston, Texas, United States, 77040

Actively Recruiting

17

Southern Endocrinology Associates

Mesquite, Texas, United States, 75149

Completed

18

Consano Clinical Research, LLC

Shavano Park, Texas, United States, 78231

Completed

19

Texas Valley Clinical Research

Weslaco, Texas, United States, 78596

Actively Recruiting

20

Chrysalis Clinical Research

St. George, Utah, United States, 84790

Actively Recruiting

21

Cicemo Srl

Buenos Aires, Argentina, 1424

Actively Recruiting

22

CIPREC

Buenos Aires, Argentina, C1119ACN

Actively Recruiting

23

Mautalen Salud e Investigación

Buenos Aires, Argentina, C1128AAF

Actively Recruiting

24

Centro Medico Dra. Laura Maffei- Investigacion Clinica Aplicada

Buenos Aires, Argentina, C1425AGC

Actively Recruiting

25

Instituto Centenario

CABA, Argentina, 1204

Actively Recruiting

26

Instituto Médico Catamarca IMEC

Rosario, Argentina, 2000

Actively Recruiting

Loading map...

Research Team

T

Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or

P

Physicians interested in becoming principal investigators please contact

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

Similar Trials

24-hour Movement Behaviors Among Adults with Type 2 Diabetes...

Diabetes Mellitus, Type 2

Actively Recruiting

1 location

A Multiple Dose Clinical Study to Evaluate the Safety, Toler...

Diabetes Mellitus, Type 2

Actively Recruiting

4 locations

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here