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Oral Combination of Glimepiride/Vildagliptin/Metformin in Patients With T2D and Dual Treatment Failure

Primary Purpose

Type 2 Diabetes

Status
Unknown status
Phase
Phase 3
Locations
Mexico
Study Type
Interventional
Intervention
Glimepiride / Vildagliptin / Metformin (2 mg/ 50 mg/ 1000 mg)
Glimepiride / Vildagliptin / Metformin (4 mg/ 50 mg/ 1000 mg)
Sponsored by
Laboratorios Silanes S.A. de C.V.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Type 2 Diabetes focused on measuring Type 2 diabetes, Combine therapy, Hypoglycemic agents

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Male or Female.
  • Age >18 years old at the beginning of the study.
  • Diagnosis of type 2 diabetes prior to the start of the study.
  • Therapeutic failure to a dual treatment with SGLT2 / Metformin, Biguanide / Sulfonylurea, Sulfonylurea / iDPP4, Biguanide / iDPP4.
  • HbA1c ≥ 7.5% and ≤ 11% during screening tests.
  • Women of childbearing potential using a contraceptive method (barrier, oral hormonal, injectable, subdermal) or naturally or surgically sterile in menopause.
  • Subject agree to participate in the study and give informed consent in writing.

Exclusion Criteria:

  • The drug is contraindicated for medical reasons.
  • History of Type 1 Diabetes Mellitus.
  • History of metabolic complications such as ketoacidosis or nonketotic hyperosmolar state.
  • History of gastric bariatric surgery or gastric band in the last year.
  • History of drug or alcohol abuse in the past year.
  • Body Mass Index <20 kg/m2 and >40 kg/m2.
  • Acute or severe renal dysfunction (glomerular filtration <30 ml / min / 1.72 m2).
  • History of chronic liver disease or ALT and / or AST ≥3 times the normal upper limit and / or Total Bilirubin> 2.5 times the upper limit of normal, or GGT ≥3 times the upper limit of normal.
  • Pregnant and / or lactating women.
  • The patient is participating in another clinical study involving an investigational treatment or participated in one in the previous 4 weeks.
  • At medical criteria, a disease that affects the prognosis and prevents outpatient management, for example, but not restricted to: end-stage cancer, kidney, heart, respiratory or liver failure, mental illness, with scheduled surgical or hospital procedures.
  • Be a patient with a working relationship with the main researcher or the research center or deprived of liberty.

Sites / Locations

  • Centro de Investigación y Avances Médicos Especializados
  • Mérida Investigación Clínica
  • Centro de Investigación Médica Aguascalientes
  • Oaxaca Site Management Organization SC.
  • Oncológico Potosino

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Group A: Glimepiride (2mg) / Vildagliptin (50mg) / Metformin (1000mg)

Group B: Glimepiride (2mg) / Vildagliptin (50mg) / Metformin (1000mg)

Arm Description

Tablets, orally, once a day

Tablets, orally, once a day

Outcomes

Primary Outcome Measures

Compare changes in HbA1
Mean change in HbA1c
Proportion of patients who change their HbA1c concentration
Proportion of patients who change their HbA1c by at least 1 percent
Mean difference change between groups in HbA1c concentration
Difference greater than 0.3 between group A and B HbA1c concentration

Secondary Outcome Measures

Mean glucose change
Compare changes in glucose between baseline, 3 and 6 months of treatment
Incidence of adverse events and reactions
Description of al the adverse events and reactions presented during the study

Full Information

First Posted
April 6, 2021
Last Updated
June 8, 2021
Sponsor
Laboratorios Silanes S.A. de C.V.
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1. Study Identification

Unique Protocol Identification Number
NCT04841096
Brief Title
Oral Combination of Glimepiride/Vildagliptin/Metformin in Patients With T2D and Dual Treatment Failure
Official Title
Efficacy and Safety of the Oral Combined Therapy Glimepiride / Vildagliptin / Metformin in Patients With Type 2 Diabetes With Dual Treatment Failure
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Unknown status
Study Start Date
June 2021 (Anticipated)
Primary Completion Date
August 2021 (Anticipated)
Study Completion Date
March 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Laboratorios Silanes S.A. de C.V.

4. Oversight

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

5. Study Description

Brief Summary
Phase IIIb, randomized, multicenter, double-blind, prospective study to evaluate the efficacy and safety of a daily fixed-dose combination of glimepiride / vildagliptin / metformin in patients with type 2 diabetes with a history of dual treatment failure and combined or individual oral antidiabetics with SGLT2 / Metformin, Biguanide / Sulfonylurea, Sulfonylurea / iDPP4 or Biguanide / iDPP4. To evaluate the changes in the percentage of HbA1c at 3 and 6 months with regard to their baseline measurement.
Detailed Description
To achieve glycemic control goals, a combination of medications with complementary mechanisms of action, with fasting and postprandial effects, may be required to achieve and maintain clinically acceptable glycemic control in some patients. A fixed combination of two or more therapeutic agents with complementary mechanisms of action makes it possible to optimize compliance and adherence to treatment among patients with T2D because it is administered once a day with the same efficacy of the separate components, but with fewer gastrointestinal effects. This is reflected in a reduction in HA1c and a lower evolution to long-term complications of T2D. Phase IIIb, randomized, multicenter, double-blind, prospective study to evaluate the efficacy and safety of a daily fixed-dose combination of glimepiride / vildagliptin / metformin in patients with type 2 diabetes with a history of dual treatment failure and combined or individual oral antidiabetics with SGLT2 / Metformin, Biguanide / Sulfonylurea, Sulfonylurea / iDPP4 or Biguanide / iDPP4.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes
Keywords
Type 2 diabetes, Combine therapy, Hypoglycemic agents

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Group A: Glimepiride (2mg) / Vildagliptin (50mg) / Metformin (1000mg)
Arm Type
Experimental
Arm Description
Tablets, orally, once a day
Arm Title
Group B: Glimepiride (2mg) / Vildagliptin (50mg) / Metformin (1000mg)
Arm Type
Experimental
Arm Description
Tablets, orally, once a day
Intervention Type
Drug
Intervention Name(s)
Glimepiride / Vildagliptin / Metformin (2 mg/ 50 mg/ 1000 mg)
Other Intervention Name(s)
G/V/M (1)
Intervention Description
Take one tablet of the prescribed dose of the investigational drug by mouth, preferably with food and in the morning
Intervention Type
Drug
Intervention Name(s)
Glimepiride / Vildagliptin / Metformin (4 mg/ 50 mg/ 1000 mg)
Other Intervention Name(s)
G/V/M (2)
Intervention Description
take one tablet of the prescribed dose of the investigational drug by mouth, preferably with food and in the morning
Primary Outcome Measure Information:
Title
Compare changes in HbA1
Description
Mean change in HbA1c
Time Frame
baseline, 3 and 6 months of treatment
Title
Proportion of patients who change their HbA1c concentration
Description
Proportion of patients who change their HbA1c by at least 1 percent
Time Frame
baseline, 3 and 6 months of treatment
Title
Mean difference change between groups in HbA1c concentration
Description
Difference greater than 0.3 between group A and B HbA1c concentration
Time Frame
baseline, 3 and 6 months of treatment
Secondary Outcome Measure Information:
Title
Mean glucose change
Description
Compare changes in glucose between baseline, 3 and 6 months of treatment
Time Frame
baseline, 3 and 6 months of treatment
Title
Incidence of adverse events and reactions
Description
Description of al the adverse events and reactions presented during the study
Time Frame
baseline, 3 and 6 months of treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Male or Female. Age >18 years old at the beginning of the study. Diagnosis of type 2 diabetes prior to the start of the study. Therapeutic failure to a dual treatment with SGLT2 / Metformin, Biguanide / Sulfonylurea, Sulfonylurea / iDPP4, Biguanide / iDPP4. HbA1c ≥ 7.5% and ≤ 11% during screening tests. Women of childbearing potential using a contraceptive method (barrier, oral hormonal, injectable, subdermal) or naturally or surgically sterile in menopause. Subject agree to participate in the study and give informed consent in writing. Exclusion Criteria: The drug is contraindicated for medical reasons. History of Type 1 Diabetes Mellitus. History of metabolic complications such as ketoacidosis or nonketotic hyperosmolar state. History of gastric bariatric surgery or gastric band in the last year. History of drug or alcohol abuse in the past year. Body Mass Index <20 kg/m2 and >40 kg/m2. Acute or severe renal dysfunction (glomerular filtration <30 ml / min / 1.72 m2). History of chronic liver disease or ALT and / or AST ≥3 times the normal upper limit and / or Total Bilirubin> 2.5 times the upper limit of normal, or GGT ≥3 times the upper limit of normal. Pregnant and / or lactating women. The patient is participating in another clinical study involving an investigational treatment or participated in one in the previous 4 weeks. At medical criteria, a disease that affects the prognosis and prevents outpatient management, for example, but not restricted to: end-stage cancer, kidney, heart, respiratory or liver failure, mental illness, with scheduled surgical or hospital procedures. Be a patient with a working relationship with the main researcher or the research center or deprived of liberty.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jorge A González, PhD
Phone
5254883785
Ext
3761
Email
jogonzalez@silanes.com.mx
First Name & Middle Initial & Last Name or Official Title & Degree
Yulia Romero-Antonio, B.S.
Phone
5554883700
Ext
3777
Email
yromero@silanes.com.mx
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Salvador Pérez Jaime, M.D
Organizational Affiliation
Centro de Investigación Médica Aguascalientes (Red OSMO)
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Juan A Becerra Hernández, M.D
Organizational Affiliation
Centro de Investigación y Avances Médicos Especializados (Red OSMO)
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ana L Flores Barranco, M.D
Organizational Affiliation
Oaxaca Site Management Organization SC. (Red OSMOS)
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Abraham S Álvarez, M.D
Organizational Affiliation
Oncológico Potosino (Red OSMO)
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Victor C Bohórquez López, M.D
Organizational Affiliation
Mérida Investigación Clínica (Red OSMO)
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centro de Investigación y Avances Médicos Especializados
City
Cancún
State/Province
Quintana Roo
ZIP/Postal Code
77506
Country
Mexico
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Juan A Becerra Hernández, M.D
Phone
998 138 2821
Facility Name
Mérida Investigación Clínica
City
Merida
State/Province
Yucatan
ZIP/Postal Code
97125
Country
Mexico
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Victor C Bohórquez López, M.D
Phone
999 688 9735
Facility Name
Centro de Investigación Médica Aguascalientes
City
Aguascalientes
ZIP/Postal Code
20116
Country
Mexico
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Salvador Pérez Jaime, M.D
Phone
449 994 9458
Facility Name
Oaxaca Site Management Organization SC.
City
Oaxaca
ZIP/Postal Code
68000
Country
Mexico
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ana L Flores Barranco, M.D
Phone
951 514 7056
Facility Name
Oncológico Potosino
City
San Luis Potosí
ZIP/Postal Code
78250
Country
Mexico
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Abraham S Álvarez, M.D
Phone
444 139 7700

12. IPD Sharing Statement

Plan to Share IPD
No
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Citation
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15850551
Citation
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Oral Combination of Glimepiride/Vildagliptin/Metformin in Patients With T2D and Dual Treatment Failure

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