Skip to main content

A Study of Insulin Efsitora Alfa (LY3209590) Compared With Insulin Degludec in Participants With Type 2 Diabetes Currently Treated With Basal Insulin

Completed · Phase 3 · NCT05275400

Conditions: Type 2 Diabetes

At a glance

Research payments reported, 2025
$32,627
U.S. investigators named
11
Sites paid
11
Planned or actual enrollment
986

About the trial

Sponsor
Eli Lilly and Company
Tested
Insulin Efsitora Alfa (drug), Insulin Degludec (drug)
Dates
Started 2022-03-08; completion 2024-05-15
Results posted
Yes

The reason for this study is to see if the study drug insulin efsitora alfa (LY3209590) is safe and effective in participants with Type 2 diabetes that have already been treated with basal insulin. The study consists of a 3-week screening/lead-in period, a 78-week treatment period and a 5-week safety follow-up period. The study will last up to 86 weeks.

From ClinicalTrials.gov, last updated 2025-06-03. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Eli Lilly and Company reported $32,627 in research payments for this study in 2025 (13 payments).

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

  • Sky Clinical Research Network Group $14,775
  • Cr Services Acquisition US LLC $5,295
  • Clinvest Research LLC $4,674
  • John Muir Med Fndtn DBA John Muir Phys Network $4,338
  • Headlands Research California LLC $1,340
  • Healthpartners Institute for Education $1,203
  • Alliance for Multispecialty Research Lls $411
  • Texas Diabetes and Endocrinology PA $241
  • Iowa Diabetes and Endocrinology Rsrch Cntr $200
  • Helena W Rodbard, MD, PA $85
  • Nyc Research Inc $65

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.