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Type 2 Diabetes MellitusPhase 3NCT03115112

Safety and Efficacy of Bexagliflozin Compared to Sitagliptin as Add-on Therapy to Metformin in Type 2 Diabetes Subjects

A Phase 3 study testing Bexagliflozin and Sitagliptin in people with Type 2 Diabetes Mellitus, run by Theracos at 56 sites in 6 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this study is to investigate the effect of bexagliflozin compared to sitagliptin as an add-on therapy to metformin in lowering hemoglobin A1c (HbA1c) levels in subjects with type 2 diabetes mellitus (T2DM). Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Type 2 Diabetes Mellitus
What is being tested?
Bexagliflozin and Sitagliptin
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
386 participants
Where
56 sitesin 6 countries
Study dates
12 Oct 2017to 31 Oct 2018
Phase
Phase 3
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Each subject was required to meet the following criteria at the time of enrollment to be eligible for the study:

  1. To have been male or female adults ≥ 18 years of age.
  2. To have been negative on the urine pregnancy test and agreed to abstain from coitus or use contraception during the entire study if a subject was female of childbearing potential.
  3. To have had a diagnosis of T2DM with HbA1c levels between 7.0% and 11% (inclusive) at the time of screening.
  4. To have been treated with a stable dose of ≥ 1500 mg/day metformin only along with diet and exercise counseling for at least 8 weeks at the time of screening.
  5. To have had a BMI ≤ 45 kg per m2 at the time of screening.
  6. To have been taking stable doses of treatment for dyslipidemia and/or hypertension for 30 days if applicable.
  7. To have been willing and able to return for all clinic visits and to complete all study-required procedures.
  8. To have adhered to the investigational product administration requirements as evidenced by missing no more than 1 day of run-in medications.

Potential subjects who exhibited any of the following characteristics were to be excluded from the study:

  1. Diagnosis of type 1 diabetes mellitus or maturity-onset diabetes of the young (MODY)
  2. Hemoglobinopathy that affected HbA1c measurement
  3. Any contraindication to the safe use of DPP-4 therapy or sitagliptin, including known hypersensitivity reaction
  4. History of pancreatitis
  5. Genitourinary tract infection within 6 weeks of screening or history of ≥ 3 genitourinary infections requiring treatment within 6 months from the time of screening
  6. Cancer, active or in remission, for < 3 years
  7. History of alcohol or illicit drug abuse in the past 2 years
  8. Triglycerides > 500 mg dL-1 at Visit V1
  9. Evidence of abnormal liver function tests (total bilirubin or alkaline phosphatase > 1.5 x upper limit of normal (ULN) with the exception of isolated Gilbert's syndrome); or alanine aminotransferase (ALT) or aspartate aminotransferase (AST) > 2.5 x ULN
  10. Estimated GFR, as calculated by the modification of diet in renal disease study equation (MDRD), < 60 mL min-1 per 1.73 m2 at the time of screening.
  11. Uncontrolled hypertension (SBP > 160 mm Hg or diastolic BP > 95 mm Hg) at Visit V1
  12. Life expectancy < 2 years
  13. History of MI, unstable angina, stroke or hospitalization for heart failure within 3 months at the time of screening
  14. History of treatment with an investigational drug within 30 days or within 7 half-lives of the investigational drug, whichever is longer
  15. Previous treatment with bexagliflozin or EGT0001474 study drug
  16. Currently or within 3 months of taking any SGLT2 inhibitor
  17. Currently participating in another interventional trial
  18. Prior renal transplantation or evidence of nephrotic syndrome (defined as a urine albumin-to-creatinine ratio (UACR) > 1500 mg g-1 at the time of screening).
  19. Any condition, disease, disorder or clinically relevant abnormality that could have jeopardized the subject's appropriate participation in this study or obscure the effects of treatment
  20. Female subjects who were pregnant or nursing
  21. Two or more consecutive SMBG measures ≥ 250 mg dL-1 (13.9 mmol L-1) prior to randomization accompanied by clinical signs or symptoms of hyperglycemia prior to randomization, including weight loss, blurred vision, increased thirst increased urination, or fatigue

Trial locations and contacts

56 sites in 6 countries.

56 sites in 6 countries

Poland13 sites
  • Clinical Research Site 7137

    Gdansk, 80-858

  • Clinical Research Site 7144

    Krakow, 30-015

  • Clinical Research Site 7142

    Krakow, 31-209

  • Clinical Research Site 7139

    Krakow, 31-261

  • Clinical Research Site 7141

    Krakow, 31-530

  • Clinical Research Site 7120

    Lublin, 20-362

  • Clinical Research Site 7138

    Lublin, 20-538

  • Clinical Research Site 7131

    Olsztyn, 10-117

  • Clinical Research Site 7143

    Poznan, 60-819

  • Clinical Research Site 7140

    Poznan, 60-821

  • Clinical Research Site 7136

    Poznan, 61-655

  • Clinical Research Site 7107

    Puławy, 24-100

  • Clinical Research Site 7128

    Torun, 87-100

Other trials in Poland

Japan12 sites
  • Clinical Research Site 6031

    Chiba, 260-0804

  • Clinical Research Site 6037

    Chiba, 272-8516

  • Clinical Research Site 6042

    Chiba, 277-0825

  • Clinical Research Site 6040

    Fukuoka, 819-0006

  • Clinical Research Site 6035

    Fukuoka, 819-0168

  • Clinical Research Site 6034

    Ibaraki, 300-0835

  • Clinical Research Site 6039

    Ibaraki, 300-1207

  • Clinical Research Site 6041

    Ibaraki, 306-0232

  • Clinical Research Site 6032

    Ibaraki, 310-0826

  • Clinical Research Site 6033

    Ōsaka, 582-0005

  • Clinical Research Site 6036

    Shizuoka, 424-0855

  • Clinical Research Site 6038

    Tochigi, 323-0022

Other trials in Japan

United States10 sites
  • Clinical Research Site 1009

    Berlin, New Jersey, 08009

  • Clinical Research Site 1271

    Chicago, Illinois, 60611

  • Clinical Research Site 1357

    Lincoln, California, 95648

  • Clinical Research Site 1358

    Long Beach, California, 90806

  • Clinical Research Site 1008

    Munroe Falls, Ohio, 44262

  • Clinical Research Site 1031

    Port Orange, Florida, 32127

  • Clinical Research Site 1360

    San Antonio, Texas, 78258

  • Clinical Research Site 1361

    San Dimas, California, 91773

  • Clinical Research Site 1359

    Topeka, Kansas, 66606

  • Clinical Research Site 1037

    Trenton, New Jersey, 08611

Other trials in United States

Spain10 sites
  • Clinical Research Site 9002

    Alicante, 03004

  • Clinical Research Site 9016

    Almería, 04001

  • Clinical Research Site 9005

    Alzira, 46600

  • Clinical Research Site 9017

    Barcelona, 08023

  • Clinical Research Site 9013

    Barcelona, 08500

  • Clinical Research Site 9012

    Madrid, 28007

  • Clinical Research Site 9011

    Seville, 41009

  • Clinical Research Site 9014

    Seville, 41013

  • Clinical Research Site 9015

    Seville

  • Clinical Research Site 9018

    Valencia, 46010

Other trials in Spain

Hungary6 sites
  • Clinical Research Site 9102

    Balatonfüred

  • Clinical Research Site 9101

    Balatongyörök

  • Clinical Research Site 9106

    Budapest

  • Clinical Research Site 9107

    Szeged

  • Clinical Research Site 9105

    Zalaegerszeg

  • Clinical Research Site 9103

    Zamárdi

Other trials in Hungary

Czechia5 sites
  • Clinical Research Site 3119

    Hodonín, 695 00

  • Clinical Research Site 3123

    Mladá Boleslav, 293 01

  • Clinical Research Site 3120

    Olomouc, 779 00

  • Clinical Research Site 3112

    Prague, 181 00

  • Clinical Research Site 3122

    Prostějov, 796 01

Other trials in Czechia

About this study

Official title: A Phase 3, Randomized, Double-Blind, Active-Controlled Study to Evaluate the Effects of Bexagliflozin Versus Sitagliptin in Subjects With Type 2 Diabetes Mellitus Who Have Inadequate Glycemic Control by Metformin

The purpose of this study is to investigate the effect of bexagliflozin compared to sitagliptin as an add-on therapy to metformin in lowering hemoglobin A1c (HbA1c) levels in subjects with type 2 diabetes mellitus (T2DM).

Read the detailed description

This was a phase 3, multi-center, randomized, double-blind, parallel-group study to demonstrate that bexagliflozin was non-inferior to sitagliptin as add-on therapy in subjects whose T2DM was not adequately controlled by metformin treatment alone. The primary effectiveness endpoint was the change in HbA1c from baseline at week 24.

At the time of screening, all subjects were to have taken metformin at a stable dose of ≥ 1500 mg per day for ≥ 8 weeks and have received diet and exercise counseling. A total of 374 eligible subjects were to be enrolled in the study. Subjects who successfully completed a 1-week run-in and who met all eligibility criteria were to be randomized in a 1:1 ratio to receive once daily double-blind treatment of either active bexagliflozin tablets with placebo sitagliptin tablets or placebo bexagliflozin tablets and active sitagliptin tablets. The study subjects were to continue receiving open-labeled metformin during the entire study at a stable dose and frequency. The treatment period was 24 weeks and was conducted in an outpatient setting.

Randomization was stratified by HbA1c (≤ 8.5% vs. ˃ 8.5%) values. Symptoms and blood sugars related to the occurrence of hyperglycemia, hypoglycemic events or symptoms that could indicate ketoacidosis were to be recorded. Bexagliflozin tablets, 20 mg or placebo, and sitagliptin tablets, 100 mg or placebo, were to be taken once daily at approximately the same time each day either before or after breakfast. Background metformin was to be taken at the same dose and frequency from screening throughout the entire study.

Each subject was advised to return to the clinic at weeks 6, 12, 18 and 24 for efficacy assessment and safety monitoring, including review of AEs and concomitant medication, vital signs, ECG, physical examination and blood and urine specimen collections. Subjects were to return to the clinic for a follow-up exit visit at week 26 or 2 weeks after the last dose of study drugs if subjects withdrew from the study prior to week 24.

Being tested
Bexagliflozin, Sitagliptin, Placebo for sitagliptin, Placebo for bexagliflozin
Medical subject headings
Diabetes Mellitus, Type 2

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • BexagliflozinDrug

    Also called EGT0001442, EGT0001474

    tablets containing 20 mg bexagliflozin

  • SitagliptinDrug

    Also called Januvia

    tablets containing 100 mg sitagliptin

  • Placebo for sitagliptinDrug

    inactive tablets to match the appearance of sitagliptin tablets

  • Placebo for bexagliflozinDrug

    inactive tablets to match the appearance of bexagliflozin tablets

Study groups in NCT03115112
Study groupRoleWhat they receive
BexagliflozinActive comparatorSubjects will receive a bexagliflozin tablet, 20 mg, once daily for the duration of the study. Subjects will continue taking metformin and receive placebo for sitagliptin daily for the duration of the study.
Receives: Drug: Bexagliflozin; Drug: Placebo for sitagliptin
SitagliptinActive comparatorSubjects will receive a sitagliptin tablet, 100 mg, once daily for the duration of the study. Subjects will continue taking metformin and receive placebo for bexagliflozin for the duration of the study.
Receives: Drug: Sitagliptin; Drug: Placebo for bexagliflozin

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in HbA1c From Baseline to Week 24

    The primary efficacy objective is to demonstrate that bexagliflozin is non-inferior to sitagliptin by evaluating the treatment effect on hemoglobin A1c (HbA1c) reduction at week 24 in subjects whose type 2 diabetes mellitus (T2DM) is inadequately controlled by metformin.

    Measured: Baseline to week 24

Secondary outcomes (3)
  1. Change in FPG From Baseline at Week 24

    To evaluate the treatment effect of bexagliflozin vs. sitagliptin on the change in fasting plasma glucose (FPG) at week 24

    Measured: Baseline to week 24

  2. Change in Body Weight in Subjects With Baseline BMI ≥ 25 kg/m2 at Week 24

    To evaluate the treatment effect of bexagliflozin vs. sitagliptin on the change in body weight in subjects with baseline body mass index (BMI) ≥ 25 kg/m2 at week 24

    Measured: Baseline to week 24

  3. Change in SBP in Subjects From Baseline at Week 24

    To evaluate the treatment effect of bexagliflozin vs. sitagliptin on the change in systolic blood pressure (SBP) in subjects at week 24

    Measured: Baseline to week 24

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted14 Apr 2017
  2. Study start12 Oct 2017
  3. Primary completion31 Oct 2018
  4. Study completion31 Oct 2018

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
386 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03115112
Sponsor's protocol ID
THR-1442-C-423
Status last verified
Jun 2021
First submitted
11 Apr 2017
Last updated
22 Jun 2021
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Bexagliflozin and Sitagliptin in people with Type 2 Diabetes Mellitus, run by Theracos at 56 sites in 6 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 22 Jun 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 56 sites in Poland, Japan, United States, Spain, Hungary and 1 more country. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 4 Jun 2021). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in HbA1c From Baseline to Week 24 (time frame: Baseline to week 24). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Jun 2021.

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