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Terminated Phase 3 Interventional Results available

Efficacy and Safety of Efpeglenatide Versus Dulaglutide in Patients With Type 2 Diabetes Mellitus Inadequately Controlled With Metformin

ClinicalTrials.gov ID: NCT03684642

Public ClinicalTrials.gov record NCT03684642. 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 May 13, 2026, 10:25 AM 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 56-week, Multicenter, Open-label, Active-controlled, Randomized Study to Evaluate the Efficacy and Safety of Efpeglenatide Once Weekly Compared to Dulaglutide Once Weekly in Patients With Type 2 Diabetes Mellitus Inadequately Controlled With Metformin

Study identification

NCT ID
NCT03684642
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Sanofi
Industry
Enrollment
908 participants

Conditions and interventions

Interventions

  • Background therapy Metformin Drug
  • Dulaglutide Drug
  • Efpeglenatide Drug

Drug

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
Sep 25, 2018
Primary completion
Oct 12, 2020
Completion
Nov 16, 2020
Last update posted
Oct 31, 2021

2018 – 2020

United States locations

U.S. sites
30
U.S. states
18
U.S. cities
28
Facility City State ZIP Site status
Investigational Site Number 8400038 Birmingham Alabama 35211
Investigational Site Number 8400035 Chandler Arizona 85224
Investigational Site Number 8400005 Glendale Arizona 85306
Investigational Site Number 8400054 Peoria Arizona 85381
Investigational Site Number 8400057 Huntington Park California 90255
Investigational Site Number 8400009 Los Angeles California 90057
Investigational Site Number 8400007 San Diego California 92120
Investigational Site Number 8400045 Spring Valley California 91978
Investigational Site Number 8400040 Tustin California 92780
Investigational Site Number 8400026 Van Nuys California 91405
Investigational Site Number 8400050 Waterbury Connecticut 06708
Investigational Site Number 8400055 Orlando Florida 32825
Investigational Site Number 8400041 Pembroke Pines Florida 33026
Investigational Site Number 8400025 Lawrenceville Georgia 30044
Investigational Site Number 8400060 Meridian Idaho 83642
Investigational Site Number 8400059 Skokie Illinois 60077
Investigational Site Number 8400044 Lexington Kentucky 40503
Investigational Site Number 8400061 Boston Massachusetts 02115
Investigational Site Number 8400001 Bridgeton New Jersey 08302
Investigational Site Number 8400039 New Windsor New York 12553
Investigational Site Number 8400028 Burlington North Carolina 27215
Investigational Site Number 8400036 Morehead City North Carolina 28557
Investigational Site Number 8400013 Maumee Ohio 43537
Investigational Site Number 8400014 Goose Creek South Carolina 29445
Investigational Site Number 8400030 Dallas Texas 75230
Investigational Site Number 8400020 San Antonio Texas 78218
Investigational Site Number 8400043 San Antonio Texas 78229
Investigational Site Number 8400053 San Antonio Texas 78258
Investigational Site Number 8400037 Layton Utah 84041
Investigational Site Number 8400049 Manassas Virginia 20110

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 15 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03684642, 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 Oct 31, 2021 · Synced May 13, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03684642 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →