Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Terminated Phase 3 Interventional Results available

Efficacy and Safety of Efpeglenatide Versus Placebo in Patients With Type 2 Diabetes Mellitus Inadequately Controlled With Basal Insulin Alone or in Combination With Oral Antidiabetic Drug(s)

ClinicalTrials.gov ID: NCT03713684

Public ClinicalTrials.gov record NCT03713684. 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 18, 2026, 4:35 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, Double-blind, Placebo-controlled, Randomized Study to Evaluate the Efficacy and Safety of Efpeglenatide Once Weekly in Patients With Type 2 Diabetes Mellitus Inadequately Controlled With Basal Insulin Alone or in Combination With Oral Antidiabetic Drug(s)

Brief summary

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

Primary Objective: To demonstrate the superiority of once weekly injection of efpeglenatide in comparison to placebo in glycated hemoglobin (HbA1c) change in participants with type 2 diabetes mellitus (T2DM) inadequately controlled with basal insulin alone or in combination with oral antidiabetic drugs (OADs). Secondary Objectives: * To demonstrate the superiority of once weekly injection of efpeglenatide in comparison to placebo on glycemic control. * To demonstrate the superiority of once weekly injection of efpeglenatide in comparison to placebo on body weight. * To evaluate the safety of once weekly injection of efpeglenatide.

Study identification

NCT ID
NCT03713684
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Sanofi
Industry
Enrollment
370 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
Nov 9, 2018 (Actual)
Primary completion
Nov 20, 2020 (Actual)
Completion
Jan 4, 2021 (Actual)
Last update posted
Dec 2, 2021

2018 – 2021

United States locations

U.S. sites
22
U.S. states
13
U.S. cities
21
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 8400057 Huntington Park California 90255 —
Investigational Site Number 8400058 La Jolla California 92037 —
Investigational Site Number 8400009 Los Angeles California 90057 —
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 8400055 Orlando Florida 32825 —
Investigational Site Number 8400041 Pembroke Pines Florida 33026 —
Investigational Site Number 8400025 Lawrenceville Georgia 30044 —
Investigational Site Number 8400052 West Des Moines Iowa 50265 —
Investigational Site Number 8400044 Lexington Kentucky 40503 —
Investigational Site Number 8400001 Bridgeton New Jersey 08302 —
Investigational Site Number 8400039 New Windsor New York 12553 —
Investigational Site Number 8400036 Morehead City North Carolina 28557 —
Investigational Site Number 8400013 Maumee Ohio 43537 —
Investigational Site Number 8400030 Dallas Texas 75230 —
Investigational Site Number 8400063 Dallas Texas 75390-9302 —
Investigational Site Number 8400043 San Antonio Texas 78229 —
Investigational Site Number 8400037 Layton Utah 84041 —

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 25 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03713684, 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 Dec 2, 2021 · Synced Oct 18, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03713684 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →