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Diabetes Study of Linagliptin and Empagliflozin in Children and Adolescents (DINAMO)TM

Primary Purpose

Diabetes Mellitus, Type 2

Status
Completed
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
Linagliptin
Empagliflozin
Placebo
Sponsored by
Boehringer Ingelheim
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus, Type 2

Eligibility Criteria

10 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients aged 10 to 17 years (inclusive) at the time of randomisation (Visit 2)
  • Male and female patients
  • Women of childbearing potential (WOCBP) must be ready and able to use highly effective methods of birth control per ICH M3 (R2) that result in a low failure rate of less than 1% per year when used consistently and correctly. A list of contraception methods meeting these criteria is provided in the patient's legal representative information sheet.
  • Signed and dated written informed consent provided by the patient's parent(s) (or legal guardian) and patient's assent in accordance with ICH-GCP and local legislation prior to admission to the trial (informed assent will be sought according to the patient's age, level of maturity, competence and capacity)
  • Documented diagnosis of T2DM at Visit 1A:

    • DINAMO TM: Documented diagnosis of T2DM for at least 8 weeks at Visit 1A
    • DINAMO TM Mono: Confirmation of T2DM at Visit 1A
  • Insufficient glycaemic control as measured by the central laboratory at Visit 1A:

    • DINAMO TM: HbA1c ≥ 6.5% and ≤ 10.5%
    • DINAMO TM Mono: HbA1c ≥ 6.5% and ≤ 9.0%
  • DINAMO TM: Patients treated with

    • diet and exercise plus metformin at a stable dose for 8 weeks prior to Visit 2 or not tolerating metformin (defined as patients who were on metformin treatment for at least 1 week and had to discontinue metformin due to metformin-related side effects as assessed by the investigator) AND/OR
    • diet and exercise plus stable basal or MDI insulin therapy,, defined as a weekly average variation of the basal insulin dose ≤ 0.1 IU/kg over 8 weeks prior to Visit 2. - DINAMOTM Mono: Drug-naïve patients or patients not on active treatment (including discontinuation of metformin due to intolerance [or previous discontinuation for other reasons] and/or discontinuation of insulin [insulin use must be 8 weeks or less] at investigator's discretion) prior to or at Visit 1A)
  • BMI ≥ 85th percentile for age and sex according to WHO references at Visit 1B
  • Non-fasting serum C-peptide levels ≥ 0.6 ng/ml as measured by the central laboratory at Visit 1A
  • Compliance with trial medication intake must be between 75% and 125% during the open-label placebo run-in period
  • Further inclusion criteria apply

Exclusion Criteria:

  • Any history of acute metabolic decompensation such as diabetic ketoacidosis within 8 weeks prior to Visit 1A and up to randomisation (mild to moderate polyuria at the time of randomisation is acceptable)
  • Diagnosis of monogenic diabetes (e.g. MODY)
  • History of pancreatitis
  • Diagnosis of metabolic bone disease
  • Gastrointestinal disorders that might interfere with study drug absorption according to investigator assessment
  • Secondary obesity as part of a syndrome (e.g. Prader-Willi syndrome)
  • Any antidiabetic medication (with the exception of metformin and/or insulin background therapy) within 8 weeks prior to Visit 1A and until Visit 2
  • Treatment with weight reduction medications (including anti-obesity drugs) within 3 months prior to Visit 1A and until Visit 2
  • History of weight-loss surgery or current aggressive diet regimen (according to investigator assessment) at Visit 1A and until Visit 2
  • Treatment with systemic corticosteroids for > 1 week within 4 weeks prior to Visit 1A and up to Visit 2 Inhaled or topical use of corticosteroids (e.g. for asthma/chronic obstructive pulmonary disease) is acceptable.
  • Change in dose of thyroid hormones within 6 weeks prior to Visit 1A or planned change or initiation of such therapy before Visit 2
  • Known hypersensitivity or allergy to the investigational products or their excipients
  • Impaired renal function defined as estimated Glomerular Filtration Rate (eGFR) < 60 ml/min/1.73m² (according to Zappitelli formula) as measured by the central laboratory at Visit 1A
  • Indication of liver disease defined by serum level of either alanine transaminase (ALT), aspartate transaminase (AST) or alkaline phosphatase above 3 fold upper limit of normal (ULN) at Visit 1A as measured by the central laboratory at Visit 1A
  • History of belonephobia (needle phobia)
  • Any documented active or suspected malignancy or history of malignancy within 5 years prior to Visit 1A, except appropriately treated basal cell carcinoma of the skin or in situ carcinoma of uterine cervix
  • Blood dyscrasias or any disorders causing haemolysis or unstable red blood cells (e.g. malaria, babesiosis, haemolytic anaemia)
  • Any other acute or chronic medical or psychiatric condition or laboratory abnormality that, based on investigator's judgement, would jeopardize patient safety during trial participation or would affect the study outcome
  • Medical contraindications to metformin according to the local label (for patient on metformin background therapy)
  • Patient not able or cannot be supported by his/her parent(s) or legal guardian to understand and comply with study requirements based on investigator's judgement
  • Previous randomisation in this trial
  • Currently enrolled in another investigational device or drug trial, or less than 30 days since ending another investigational device or drug trial(s), or receiving other investigational treatment(s)
  • Chronic alcohol or drug abuse within 3 months prior to Visit 1A or any condition that, in the investigator's opinion, makes them an unreliable trial patient or unlikely to complete the trial
  • Female patients who are pregnant, nursing, or who plan to become pregnant in the trial

Sites / Locations

  • Phoenix Children's Hospital
  • University of Arizona
  • CHOC Children's Hospital
  • Stanford University Medical Center
  • Rady Children's Hospital - San Diego
  • University of California San Francisco
  • Children's Hospital Colorado
  • Yale University School of Medicine
  • Empire Clinical Research, LLC
  • Oceane7 Clinical Research
  • Pediatric and Adult Research Center
  • Nemours Clinic
  • University of South Florida
  • AdventHealth Medical Group, Pediatric Diabetes and Endocrinology at Winter Park
  • Children's Center for Advanced Pediatrics
  • Atlanta Center
  • Columbus Regional Research Institute
  • Rocky Mountain Diabetes and Osteoporosis Center
  • University of Iowa Hospitals and Clinics
  • Novak Center for Children's Health
  • Johns Hopkins Hospital
  • Boston Children's Hospital
  • Joslin Diabetes Center
  • Integrative Biosciences Center
  • University Of Mississippi Medical Center
  • Children's Mercy Hospitals and Clinics
  • Advantage Clinical Trials
  • UBMD Pediatrics
  • New York University Langone Medical Center
  • SUNY Upstate Medical University
  • The University of North Carolina at Chapel Hill
  • University Hospitals of Cleveland
  • University of Oklahoma
  • University of Oklahoma
  • Penn State College of Medicine
  • Children's Hospital of Philadelphia
  • Monument Health Rapid City Hospital, Inc.
  • LifeDoc Research, PLLC
  • Vanderbilt University Medical Center
  • Office of Amir A. Hassan, MD, P.A.
  • Saenz Medical Center
  • Texas Diabetes Institute
  • University of Virginia Health System
  • Children's Hospital of Richmond at VCU
  • Sanatorio Allende S.A.
  • Hospital de Clínicas Pte. Dr. Nicolás Avellaneda
  • Instituto de Estudos e Pesquisas Clínicas IEP-CE
  • Fundacao de Apoio ao Ensino, Pesquisa e Assistencia do Hospital das Clinicas da Faculdade de Medicina de Ribeirao Preto
  • University of Manitoba - Health Sciences Centre
  • The Hospital for Sick Children
  • The First Hospital of Jilin University
  • Zhengzhou Children'S Hospital
  • Centro de Diabetes Cardiovascular IPS
  • Dexa-Diab IPS
  • Universitätsklinikum Freiburg
  • Soroka Univ. Medical Center
  • Rambam Medical Center
  • The Chaim Sheba Medical Center Tel HaShomer
  • Severance Hospital
  • Asan Medical Center
  • Ajou University Hospital
  • Investigación en Salud y Metabolismo S.C.
  • CAIMED Investigacion en Salud, S.A. de C.V.
  • Centro de Estudios de Investigación Metabólicos y Cardiovasculares, S.C.
  • Consultorio Medico
  • Investigacion Medica Sonora S.C.
  • Centro de Investigación Médica de Ocidente, S.C.
  • San Juan Bautista School of Medicine
  • Regional Clinical Hospital 'The Badge of Honor Order'
  • Ivanovo Reg.Clin.Hosp.
  • Rep.childrens clin.hosp.
  • State Medical University, Kazan
  • Munic. Instit. of HC "Kirov clin. hosp.#7 n.a.V.I.Urlova"
  • Endocrinology Scientific Center, MoH and Social Development
  • State Novosibirsk Regional Clinical Hospital
  • Fed. State Budget Educational Instit. of Higher Education "Rostov State Med. Univ." of MoH of RF
  • St. Petersburg State Pediatric University
  • Siberian State Med.Uni,Faculty Therapy Dep.w/ Clin.Pharmacol
  • Bahkir state med. Univ. of the Ministry Polyclinic Pediatric
  • Srinagarind Hospital
  • Rajavithi Hospital
  • St George's Hospital
  • Royal Berkshire Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Placebo Comparator

Arm Label

Linagliptin

Empagliflozin

Placebo

Arm Description

Linagliptin arm. Oral route. Linagliptin tablets administered once daily for 52 weeks

Empagliflozin arm. Oral route. Start with a low dose of empagliflozin administered once daily and randomly up titrate to the high dose of empagliflozin administered once daily if HbA1c ≥ 7% at week 12

Placebo arm. Oral route. Placebo tablets administered once daily up to 26 weeks and then linagliptin or low dose of empagliflozin or high dose of empagliflozin administered once daily up to 52 weeks

Outcomes

Primary Outcome Measures

DINAMO TM: Change from baseline in HbA1c (%)
DINAMO TM Mono: Occurrence of treatment failure up to or at Week 26

Secondary Outcome Measures

DINAMO TM: Change from baseline in fasting plasma glucose (mg/dl)
DINAMO TM: Change from baseline in body weight (kg)
DINAMO TM: Change from baseline in systolic blood pressure (SBP)
DINAMO TM: Change from baseline in diastolic blood pressure (DBP)
DINAMO TM: Proportion of patients who achieve HbA1c < 6.5%
DINAMO TM: Proportion of patients who achieve HbA1c < 7.0%
DINAMO TM Mono: Time to treatment failure
DINAMO TM Mono: Change in HbA1c (%) from baseline
DINAMO TM Mono: Change in FPG (mg/dL) from baseline
DINAMO TM Mono: Change in body weight (kg) from baseline
DINAMO TM Mono: Change in SBP (mmHg) from baseline
DINAMO TM Mono: Change in DBP (mmHg) from baseline
DINAMO TM Mono: Proportion of patients who achieve HbA1c < 6.5%
DINAMO TM Mono :Proportion of patients who achieve HbA1c < 7.0%

Full Information

First Posted
February 6, 2018
Last Updated
October 18, 2023
Sponsor
Boehringer Ingelheim
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1. Study Identification

Unique Protocol Identification Number
NCT03429543
Brief Title
Diabetes Study of Linagliptin and Empagliflozin in Children and Adolescents (DINAMO)TM
Official Title
A Double-blind, Randomised, Placebo-controlled, Parallel Group Trial to Evaluate the Efficacy and Safety of Empagliflozin and Linagliptin Over 26 Weeks, With a Double-blind Active Treatment Safety Extension Period up to 52 Weeks, in Children and Adolescents With Type 2 Diabetes Mellitus
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Completed
Study Start Date
March 20, 2018 (Actual)
Primary Completion Date
October 19, 2022 (Actual)
Study Completion Date
May 31, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Boehringer Ingelheim

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this research study is to evaluate the efficacy and safety of an empagliflozin dosing regimen and one dose of linagliptin in patients with type 2 diabetes who are aged 10 to below 18 years and are currently taking metformin, insulin or both drugs (DINAMO TM) or who are treatment naïve or not on active treatment after metformin withdrawal (DINAMO TM MONO) . Empagliflozin and linagliptin are both approved for use in adult patients with type 2 diabetes. This study will assess how well empagliflozin and linagliptin work by finding out how these treatments affect blood glucose (sugar) levels compared to placebo (a pill that contains no active drug), in children and adolescents. Empagliflozin and linagliptin are considered investigational products in this study since while they have been approved for use in adults, they have not been approved for children and adolescents due to lack of clinical studies in this specific population. Patients with type 2 diabetes have higher levels of blood glucose (sugar) than patients who do not have this disease. The high level of sugar in the blood can lead to serious short-term and long-term medical problems. The main goal of treating diabetic patients is to lower blood glucose to a normal level. Lowering and controlling blood glucose help prevent or delay complications of diabetes such as heart disease, kidney, eye and nerve diseases, and the possibility of amputation. Empagliflozin is a drug that helps to reduce blood glucose (sugar) levels by causing glucose to be excreted in the urines. Linagliptin works by increasing the production of insulin (a hormone that controls the level of blood glucose) after meals when blood glucose (sugar) levels are too high. This helps to lower blood sugar levels. The subject will either receive one of the active study drugs or a placebo. This study will be double blind; this means that neither the subject, nor the study doctor will know which treatment the subject will receive. Which treatment the subject receives is decided by a computer, purely by chance; this is called a "random assignment". For this study, there will first be a screening visit, followed by a 2-week placebo run-in period (all subjects will take placebo once daily). This run-in period is designed to ensure subjects are able to take the study drugs as described in the study protocol. Thereafter there will be a 26-week treatment phase (week 1-week 26) and a 26-week safety extension period (week 27-week 52). Following this there will be a follow-up visit at week 55. On Day 1 after the placebo run-in phase, the subject will be randomly assigned to receive one of the 3 treatments: empagliflozin 10 mg, linagliptin 5 mg or placebo in a blinded manner. This treatment will continue up to week 14. Then after week 14, the subject will be assigned to receive one of the following 4 treatments: empagliflozin 10 mg, empagliflozin 25 mg, linagliptin 5 mg or placebo in a blinded manner. The drugs assigned after week 14 will be the same drugs as on Day 1 but some subjects will receive a higher dose of empagliflozin. After the completion of the 26-week treatment period, the subject will enter a 26-week safety extension period. The same active treatment that the subject had been assigned to at week 14 visit will be continued. Subjects assigned to placebo on Day 1 will be randomly assigned to receive one of the 3 active treatments: empagliflozin 10 mg, empagliflozin 25 mg or linagliptin 5 mg in a blinded manner. This safety extension period is primarily designed to provide additional information on how well empagliflozin and linagliptin are tolerated. Following the treatment phases, there will be a follow-up visit at week 55 Intervention model description: Eligible subjects with HbA1c of 6.5% to 10.5% at screening will be randomized in a 1:1:1 ratio to receive empagliflozin 10 mg, linagliptin 5 mg or placebo. HbA1c assessment will be performed at Week 12. All subjects with Week 12 HbA1c < 7% will remain on previously assigned randomized treatment. Subjects taking empagliflozin with Week 12 HbA1c >= 7% will be re-randomized in a 1:1 ratio to continue on the low dose treatment (empagliflozin 10 mg) or up-titrate to the high dose treatment (empagliflozin 25 mg). Subjects taking linagliptin or placebo with Week 12 HbA1c >= 7% will remain on previously assigned treatment. All subjects will get new medication kits dispensed at Week 14 to maintain the blinding. At Week 26, all subjects previously assigned to placebo will be re-randomized in a 1:1:1: ratio to receive one of the active treatments: empagliflozin 10 mg, empagliflozin 25 mg or linagliptin 5 mg. All subjects will get new medication kits dispensed at Week 14 to maintain the blinding.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 2

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
175 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Linagliptin
Arm Type
Experimental
Arm Description
Linagliptin arm. Oral route. Linagliptin tablets administered once daily for 52 weeks
Arm Title
Empagliflozin
Arm Type
Experimental
Arm Description
Empagliflozin arm. Oral route. Start with a low dose of empagliflozin administered once daily and randomly up titrate to the high dose of empagliflozin administered once daily if HbA1c ≥ 7% at week 12
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo arm. Oral route. Placebo tablets administered once daily up to 26 weeks and then linagliptin or low dose of empagliflozin or high dose of empagliflozin administered once daily up to 52 weeks
Intervention Type
Drug
Intervention Name(s)
Linagliptin
Other Intervention Name(s)
ONDERO, TRAJENTA, TRAYENTA, TRAZENTA, TRADJENTA
Intervention Description
Film Coated Tablet
Intervention Type
Drug
Intervention Name(s)
Empagliflozin
Other Intervention Name(s)
JARDIANCE, JARDIANZ, GIBTULIO
Intervention Description
Film Coated Tablet
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Film Coated Tablet
Primary Outcome Measure Information:
Title
DINAMO TM: Change from baseline in HbA1c (%)
Time Frame
26 Weeks
Title
DINAMO TM Mono: Occurrence of treatment failure up to or at Week 26
Time Frame
Up to 26 Weeks
Secondary Outcome Measure Information:
Title
DINAMO TM: Change from baseline in fasting plasma glucose (mg/dl)
Time Frame
26 Weeks
Title
DINAMO TM: Change from baseline in body weight (kg)
Time Frame
26 Weeks
Title
DINAMO TM: Change from baseline in systolic blood pressure (SBP)
Time Frame
26 Weeks
Title
DINAMO TM: Change from baseline in diastolic blood pressure (DBP)
Time Frame
26 Weeks
Title
DINAMO TM: Proportion of patients who achieve HbA1c < 6.5%
Time Frame
26 weeks
Title
DINAMO TM: Proportion of patients who achieve HbA1c < 7.0%
Time Frame
26 Weeks
Title
DINAMO TM Mono: Time to treatment failure
Time Frame
Up to 52 Weeks
Title
DINAMO TM Mono: Change in HbA1c (%) from baseline
Time Frame
26 Weeks
Title
DINAMO TM Mono: Change in FPG (mg/dL) from baseline
Time Frame
26 Weeks
Title
DINAMO TM Mono: Change in body weight (kg) from baseline
Time Frame
26 Weeks
Title
DINAMO TM Mono: Change in SBP (mmHg) from baseline
Time Frame
26 Weeks
Title
DINAMO TM Mono: Change in DBP (mmHg) from baseline
Time Frame
26 Weeks
Title
DINAMO TM Mono: Proportion of patients who achieve HbA1c < 6.5%
Time Frame
26 Weeks
Title
DINAMO TM Mono :Proportion of patients who achieve HbA1c < 7.0%
Time Frame
26 Weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients aged 10 to 17 years (inclusive) at the time of randomisation (Visit 2) Male and female patients Women of childbearing potential (WOCBP) must be ready and able to use highly effective methods of birth control per ICH M3 (R2) that result in a low failure rate of less than 1% per year when used consistently and correctly. A list of contraception methods meeting these criteria is provided in the patient's legal representative information sheet. Signed and dated written informed consent provided by the patient's parent(s) (or legal guardian) and patient's assent in accordance with ICH-GCP and local legislation prior to admission to the trial (informed assent will be sought according to the patient's age, level of maturity, competence and capacity) Documented diagnosis of T2DM at Visit 1A: DINAMO TM: Documented diagnosis of T2DM for at least 8 weeks at Visit 1A DINAMO TM Mono: Confirmation of T2DM at Visit 1A Insufficient glycaemic control as measured by the central laboratory at Visit 1A: DINAMO TM: HbA1c ≥ 6.5% and ≤ 10.5% DINAMO TM Mono: HbA1c ≥ 6.5% and ≤ 9.0% DINAMO TM: Patients treated with diet and exercise plus metformin at a stable dose for 8 weeks prior to Visit 2 or not tolerating metformin (defined as patients who were on metformin treatment for at least 1 week and had to discontinue metformin due to metformin-related side effects as assessed by the investigator) AND/OR diet and exercise plus stable basal or MDI insulin therapy,, defined as a weekly average variation of the basal insulin dose ≤ 0.1 IU/kg over 8 weeks prior to Visit 2. - DINAMOTM Mono: Drug-naïve patients or patients not on active treatment (including discontinuation of metformin due to intolerance [or previous discontinuation for other reasons] and/or discontinuation of insulin [insulin use must be 8 weeks or less] at investigator's discretion) prior to or at Visit 1A) BMI ≥ 85th percentile for age and sex according to WHO references at Visit 1B Non-fasting serum C-peptide levels ≥ 0.6 ng/ml as measured by the central laboratory at Visit 1A Compliance with trial medication intake must be between 75% and 125% during the open-label placebo run-in period Further inclusion criteria apply Exclusion Criteria: Any history of acute metabolic decompensation such as diabetic ketoacidosis within 8 weeks prior to Visit 1A and up to randomisation (mild to moderate polyuria at the time of randomisation is acceptable) Diagnosis of monogenic diabetes (e.g. MODY) History of pancreatitis Diagnosis of metabolic bone disease Gastrointestinal disorders that might interfere with study drug absorption according to investigator assessment Secondary obesity as part of a syndrome (e.g. Prader-Willi syndrome) Any antidiabetic medication (with the exception of metformin and/or insulin background therapy) within 8 weeks prior to Visit 1A and until Visit 2 Treatment with weight reduction medications (including anti-obesity drugs) within 3 months prior to Visit 1A and until Visit 2 History of weight-loss surgery or current aggressive diet regimen (according to investigator assessment) at Visit 1A and until Visit 2 Treatment with systemic corticosteroids for > 1 week within 4 weeks prior to Visit 1A and up to Visit 2 Inhaled or topical use of corticosteroids (e.g. for asthma/chronic obstructive pulmonary disease) is acceptable. Change in dose of thyroid hormones within 6 weeks prior to Visit 1A or planned change or initiation of such therapy before Visit 2 Known hypersensitivity or allergy to the investigational products or their excipients Impaired renal function defined as estimated Glomerular Filtration Rate (eGFR) < 60 ml/min/1.73m² (according to Zappitelli formula) as measured by the central laboratory at Visit 1A Indication of liver disease defined by serum level of either alanine transaminase (ALT), aspartate transaminase (AST) or alkaline phosphatase above 3 fold upper limit of normal (ULN) at Visit 1A as measured by the central laboratory at Visit 1A History of belonephobia (needle phobia) Any documented active or suspected malignancy or history of malignancy within 5 years prior to Visit 1A, except appropriately treated basal cell carcinoma of the skin or in situ carcinoma of uterine cervix Blood dyscrasias or any disorders causing haemolysis or unstable red blood cells (e.g. malaria, babesiosis, haemolytic anaemia) Any other acute or chronic medical or psychiatric condition or laboratory abnormality that, based on investigator's judgement, would jeopardize patient safety during trial participation or would affect the study outcome Medical contraindications to metformin according to the local label (for patient on metformin background therapy) Patient not able or cannot be supported by his/her parent(s) or legal guardian to understand and comply with study requirements based on investigator's judgement Previous randomisation in this trial Currently enrolled in another investigational device or drug trial, or less than 30 days since ending another investigational device or drug trial(s), or receiving other investigational treatment(s) Chronic alcohol or drug abuse within 3 months prior to Visit 1A or any condition that, in the investigator's opinion, makes them an unreliable trial patient or unlikely to complete the trial Female patients who are pregnant, nursing, or who plan to become pregnant in the trial
Facility Information:
Facility Name
Phoenix Children's Hospital
City
Phoenix
State/Province
Arizona
ZIP/Postal Code
85016
Country
United States
Facility Name
University of Arizona
City
Tucson
State/Province
Arizona
ZIP/Postal Code
85724
Country
United States
Facility Name
CHOC Children's Hospital
City
Orange
State/Province
California
ZIP/Postal Code
92868
Country
United States
Facility Name
Stanford University Medical Center
City
Palo Alto
State/Province
California
ZIP/Postal Code
94304
Country
United States
Facility Name
Rady Children's Hospital - San Diego
City
San Diego
State/Province
California
ZIP/Postal Code
92123
Country
United States
Facility Name
University of California San Francisco
City
San Francisco
State/Province
California
ZIP/Postal Code
94158
Country
United States
Facility Name
Children's Hospital Colorado
City
Aurora
State/Province
Colorado
ZIP/Postal Code
80045
Country
United States
Facility Name
Yale University School of Medicine
City
New Haven
State/Province
Connecticut
ZIP/Postal Code
06511
Country
United States
Facility Name
Empire Clinical Research, LLC
City
Miami Lakes
State/Province
Florida
ZIP/Postal Code
33016
Country
United States
Facility Name
Oceane7 Clinical Research
City
Miami
State/Province
Florida
ZIP/Postal Code
33144
Country
United States
Facility Name
Pediatric and Adult Research Center
City
Orlando
State/Province
Florida
ZIP/Postal Code
32825
Country
United States
Facility Name
Nemours Clinic
City
Pensacola
State/Province
Florida
ZIP/Postal Code
32514
Country
United States
Facility Name
University of South Florida
City
Tampa
State/Province
Florida
ZIP/Postal Code
33612
Country
United States
Facility Name
AdventHealth Medical Group, Pediatric Diabetes and Endocrinology at Winter Park
City
Winter Park
State/Province
Florida
ZIP/Postal Code
32789
Country
United States
Facility Name
Children's Center for Advanced Pediatrics
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30329
Country
United States
Facility Name
Atlanta Center
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30331
Country
United States
Facility Name
Columbus Regional Research Institute
City
Columbus
State/Province
Georgia
ZIP/Postal Code
31904
Country
United States
Facility Name
Rocky Mountain Diabetes and Osteoporosis Center
City
Idaho Falls
State/Province
Idaho
ZIP/Postal Code
83404
Country
United States
Facility Name
University of Iowa Hospitals and Clinics
City
Iowa City
State/Province
Iowa
ZIP/Postal Code
52242
Country
United States
Facility Name
Novak Center for Children's Health
City
Louisville
State/Province
Kentucky
ZIP/Postal Code
40202
Country
United States
Facility Name
Johns Hopkins Hospital
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21287
Country
United States
Facility Name
Boston Children's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
Facility Name
Joslin Diabetes Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02215
Country
United States
Facility Name
Integrative Biosciences Center
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48202
Country
United States
Facility Name
University Of Mississippi Medical Center
City
Jackson
State/Province
Mississippi
ZIP/Postal Code
39216-4505
Country
United States
Facility Name
Children's Mercy Hospitals and Clinics
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
64108
Country
United States
Facility Name
Advantage Clinical Trials
City
Bronx
State/Province
New York
ZIP/Postal Code
10468
Country
United States
Facility Name
UBMD Pediatrics
City
Buffalo
State/Province
New York
ZIP/Postal Code
14203
Country
United States
Facility Name
New York University Langone Medical Center
City
New York
State/Province
New York
ZIP/Postal Code
10016
Country
United States
Facility Name
SUNY Upstate Medical University
City
Syracuse
State/Province
New York
ZIP/Postal Code
13210
Country
United States
Facility Name
The University of North Carolina at Chapel Hill
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27514
Country
United States
Facility Name
University Hospitals of Cleveland
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44106
Country
United States
Facility Name
University of Oklahoma
City
Oklahoma City
State/Province
Oklahoma
ZIP/Postal Code
73104
Country
United States
Facility Name
University of Oklahoma
City
Tulsa
State/Province
Oklahoma
ZIP/Postal Code
74135
Country
United States
Facility Name
Penn State College of Medicine
City
Hershey
State/Province
Pennsylvania
ZIP/Postal Code
17033
Country
United States
Facility Name
Children's Hospital of Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
Facility Name
Monument Health Rapid City Hospital, Inc.
City
Rapid City
State/Province
South Dakota
ZIP/Postal Code
57701
Country
United States
Facility Name
LifeDoc Research, PLLC
City
Memphis
State/Province
Tennessee
ZIP/Postal Code
38119
Country
United States
Facility Name
Vanderbilt University Medical Center
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37232
Country
United States
Facility Name
Office of Amir A. Hassan, MD, P.A.
City
Houston
State/Province
Texas
ZIP/Postal Code
77089
Country
United States
Facility Name
Saenz Medical Center
City
La Joya
State/Province
Texas
ZIP/Postal Code
78560
Country
United States
Facility Name
Texas Diabetes Institute
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78207
Country
United States
Facility Name
University of Virginia Health System
City
Charlottesville
State/Province
Virginia
ZIP/Postal Code
22908
Country
United States
Facility Name
Children's Hospital of Richmond at VCU
City
Richmond
State/Province
Virginia
ZIP/Postal Code
23219
Country
United States
Facility Name
Sanatorio Allende S.A.
City
Nueva Córdoba
ZIP/Postal Code
X5000JHQ
Country
Argentina
Facility Name
Hospital de Clínicas Pte. Dr. Nicolás Avellaneda
City
San Miguel de Tucumán
ZIP/Postal Code
4000
Country
Argentina
Facility Name
Instituto de Estudos e Pesquisas Clínicas IEP-CE
City
Fortaleza
ZIP/Postal Code
60160-230
Country
Brazil
Facility Name
Fundacao de Apoio ao Ensino, Pesquisa e Assistencia do Hospital das Clinicas da Faculdade de Medicina de Ribeirao Preto
City
Ribeirao Preto
ZIP/Postal Code
14048-900
Country
Brazil
Facility Name
University of Manitoba - Health Sciences Centre
City
Winnipeg
State/Province
Manitoba
ZIP/Postal Code
R3E 3P4
Country
Canada
Facility Name
The Hospital for Sick Children
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 1X8
Country
Canada
Facility Name
The First Hospital of Jilin University
City
Changchun
ZIP/Postal Code
130021
Country
China
Facility Name
Zhengzhou Children'S Hospital
City
Zhengzhou
ZIP/Postal Code
450017
Country
China
Facility Name
Centro de Diabetes Cardiovascular IPS
City
Barranquilla
ZIP/Postal Code
80020
Country
Colombia
Facility Name
Dexa-Diab IPS
City
Bogotá DC
ZIP/Postal Code
110221
Country
Colombia
Facility Name
Universitätsklinikum Freiburg
City
Freiburg
ZIP/Postal Code
79106
Country
Germany
Facility Name
Soroka Univ. Medical Center
City
Beer Sheva
ZIP/Postal Code
84101
Country
Israel
Facility Name
Rambam Medical Center
City
Haifa
ZIP/Postal Code
31096
Country
Israel
Facility Name
The Chaim Sheba Medical Center Tel HaShomer
City
Ramat-Gan
ZIP/Postal Code
5265601
Country
Israel
Facility Name
Severance Hospital
City
Seoul
ZIP/Postal Code
03722
Country
Korea, Republic of
Facility Name
Asan Medical Center
City
Seoul
ZIP/Postal Code
05505
Country
Korea, Republic of
Facility Name
Ajou University Hospital
City
Suwon
ZIP/Postal Code
16499
Country
Korea, Republic of
Facility Name
Investigación en Salud y Metabolismo S.C.
City
Chihuahua
ZIP/Postal Code
31217
Country
Mexico
Facility Name
CAIMED Investigacion en Salud, S.A. de C.V.
City
Ciudad de México
ZIP/Postal Code
06760
Country
Mexico
Facility Name
Centro de Estudios de Investigación Metabólicos y Cardiovasculares, S.C.
City
Ciudad Madero
ZIP/Postal Code
89440
Country
Mexico
Facility Name
Consultorio Medico
City
Puebla
ZIP/Postal Code
72190
Country
Mexico
Facility Name
Investigacion Medica Sonora S.C.
City
Sonora
ZIP/Postal Code
83280
Country
Mexico
Facility Name
Centro de Investigación Médica de Ocidente, S.C.
City
Zapopan
ZIP/Postal Code
45116
Country
Mexico
Facility Name
San Juan Bautista School of Medicine
City
Caguas
ZIP/Postal Code
00726
Country
Puerto Rico
Facility Name
Regional Clinical Hospital 'The Badge of Honor Order'
City
Irkutsk
ZIP/Postal Code
664049
Country
Russian Federation
Facility Name
Ivanovo Reg.Clin.Hosp.
City
Ivanovo
ZIP/Postal Code
153040
Country
Russian Federation
Facility Name
Rep.childrens clin.hosp.
City
Izhevsk
ZIP/Postal Code
426009
Country
Russian Federation
Facility Name
State Medical University, Kazan
City
Kazan
ZIP/Postal Code
420012
Country
Russian Federation
Facility Name
Munic. Instit. of HC "Kirov clin. hosp.#7 n.a.V.I.Urlova"
City
Kirov
ZIP/Postal Code
610014
Country
Russian Federation
Facility Name
Endocrinology Scientific Center, MoH and Social Development
City
Moscow
ZIP/Postal Code
117036
Country
Russian Federation
Facility Name
State Novosibirsk Regional Clinical Hospital
City
Novosibirsk
ZIP/Postal Code
630091
Country
Russian Federation
Facility Name
Fed. State Budget Educational Instit. of Higher Education "Rostov State Med. Univ." of MoH of RF
City
Rostov-on-Don
ZIP/Postal Code
344022
Country
Russian Federation
Facility Name
St. Petersburg State Pediatric University
City
St. Petersburg
ZIP/Postal Code
194100
Country
Russian Federation
Facility Name
Siberian State Med.Uni,Faculty Therapy Dep.w/ Clin.Pharmacol
City
Tomsk
ZIP/Postal Code
634050
Country
Russian Federation
Facility Name
Bahkir state med. Univ. of the Ministry Polyclinic Pediatric
City
Ufa
ZIP/Postal Code
450106
Country
Russian Federation
Facility Name
Srinagarind Hospital
City
Khon Kaen
ZIP/Postal Code
40002
Country
Thailand
Facility Name
Rajavithi Hospital
City
Krung Thep Maha Nakhon
ZIP/Postal Code
10400
Country
Thailand
Facility Name
St George's Hospital
City
London
ZIP/Postal Code
SW17 0QT
Country
United Kingdom
Facility Name
Royal Berkshire Hospital
City
Reading
ZIP/Postal Code
RG1 5AN
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
After the study is completed and the primary manuscript is accepted for publishing, researchers can use this following link https://www.mystudywindow.com/msw/datasharing to request access to the clinical study documents regarding this study, and upon a signed "Document Sharing Agreement". Also, Researchers can use the following link https://www.mystudywindow.com/msw/datasharing to find information in order to request access to the clinical study data, for this and other listed studies, after the submission of a research proposal and according to the terms outlined in the website. The data shared are the raw clinical study data sets.
IPD Sharing Time Frame
After all regulatory activities are completed in the US and EU for the product and indication, and after the primary manuscript has been accepted for publication.
IPD Sharing Access Criteria
For study documents - upon signing of a 'Document Sharing Agreement'. For study data - 1. after the submission and approval of the research proposal (checks will be performed by both the independent review panel and the sponsor, including checking that the planned analysis does not compete with sponsor's publication plan); 2. and upon signing of a 'Data Sharing Agreement'.
IPD Sharing URL
https://www.mystudywindow.com/msw/datasharing
Links:
URL
https://www.mystudywindow.com
Description
Related Info

Learn more about this trial

Diabetes Study of Linagliptin and Empagliflozin in Children and Adolescents (DINAMO)TM

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