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Safety And Efficacy Of Empagliflozin In Pakistani Muslim Population With Type Ii Diabetes Mellitus (SAFE-PAK)

Primary Purpose

Type II Diabetes Mellitus

Status
Completed
Phase
Phase 4
Locations
Pakistan
Study Type
Interventional
Intervention
Empagliflozin
Usual care group
Sponsored by
Getz Pharma
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Type II Diabetes Mellitus

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Pakistani muslim male / female, type 2 diabetic patient having age from 18 years to 75 years
  • Patient who give informed consent voluntarily
  • BMI ≤45 kg/m2
  • Glycosylated hemoglobin of 7 - ≤10%

Exclusion Criteria:

  • Patients who are on empagliflozin treatment
  • Indication of liver disease, defined by serum levels of either alanine aminotransferase, aspartate aminotransferase, and alkaline phosphatase above 3 times upper limit to normal
  • Estimated glomerular filtration rate (eGFR) <45 mL /min /1.73m2
  • History of recurrent urinary tract infection (UTI) and/or past 3 months' history of UTI and its treatment
  • Patients with positive urine culture for UTI at the time of screening
  • Patients who have been admitted to the hospital in the past 3 months for diabetic ketoacidosis (DKA) and hyperosmolar hyperglycemic state
  • Patients with past 3 months' history of fungal infection and its treatment
  • History of blood dyscrasias or any disorders causing haemolysis or unstable red blood cell
  • History of benign prostate hyperplasia
  • Any acute coronary syndrome, stroke and/or transient ischemic attack (TIA) in the previous 3 months
  • Any contraindication for patients to Biguanides, Sulfonylureas, DPP-IV inhibitors, SGLT-2 Inhibitors
  • Treatment with anti-obesity drugs or any other treatment leading to unstable body weight
  • Patients with past 6 weeks treatment history with systemic steroids or thyroid hormones or any other uncontrolled endocrine disorder except T2DM
  • Pre-menopausal women who are nursing or pregnant or are of childbearing potential and not practicing an acceptable method of birth control
  • Any other clinical condition that would jeopardize patients safety while participating in this study

Sites / Locations

  • Balochistan Medical Center
  • Lady Reading Hospital
  • Post Graduate Medical Institute
  • Hanif Medical Center
  • Shifa International Hospital
  • Diabetes Institute of Pakistan
  • Jinnah Hospital
  • National Defence Center
  • Al-Khaliq Hospital
  • Fatimiyah Hospital
  • National Institute of Cardiovascular Disease

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Empagliflozin

Usual Care Group

Arm Description

Outcomes

Primary Outcome Measures

Number of participants reported adverse events
Number of participants reported adverse events such as Hypoglycemic events, Hypotension, Dehydration, Urinary tract infection, Diabetic Ketoacidosis, Fungal infection or any other

Secondary Outcome Measures

Frequency of participants achieved HbA1c level <7%
Frequency of participants achieved HbA1c level <7%
Frequency of participants achieved FBS level within normal range
Frequency of participants achieved FBS level within normal range

Full Information

First Posted
November 27, 2020
Last Updated
December 10, 2020
Sponsor
Getz Pharma
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1. Study Identification

Unique Protocol Identification Number
NCT04665284
Brief Title
Safety And Efficacy Of Empagliflozin In Pakistani Muslim Population With Type Ii Diabetes Mellitus
Acronym
SAFE-PAK
Official Title
Safety And Efficacy Of Empagliflozin In Pakistani Muslim Population With Type Ii Diabetes Mellitus
Study Type
Interventional

2. Study Status

Record Verification Date
December 2020
Overall Recruitment Status
Completed
Study Start Date
June 1, 2019 (Actual)
Primary Completion Date
September 15, 2020 (Actual)
Study Completion Date
September 28, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Getz Pharma

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
To compare the safety and efficacy of empagliflozin versus other treatments in Pakistani Muslim population with type II diabetes mellitus.
Detailed Description
Diabetes is the one of the most common non-communicable diseases affecting 425 million adults worldwide. This figure is expected to rise to 629 million by the year 2045.1 90% of the diabetic population has type 2 diabetes. 2 As of 2018, more than 500 million individuals are residing with type 2 diabetes mellitus globally. 3 In Pakistan, the situation is similarly alarming. According to a recent survey, 16.98% of the Pakistani population has diabetes.4 The primary target of therapy in diabetes mellitus is optimum blood glucose control. In case of type 2 diabetes, this is achieved by a combination of oral hypoglycemic agents and injectable drugs with insulin as a last resort. A number of oral agents targeting various sites of action are available. Sodium-glucose cotransporter-2 (SGLT2) inhibitors are newer class of drugs that have been introduced. They have a unique mechanism of action. By acting at the sodium glucose co-transporter, they block the reabsorption of glucose leading to an increase in urinary glucose excretion and lowering of plasma glucose.5 This action is completely independent of the beta cell function. There are several theoretical advantages to this approach. In addition to lowering blood glucose, the urinary glucose excretion results in loss of calories and weight reduction and the associated osmotic diuretic effect can aid in lowering blood pressures.6,7 Numerous studies have demonstrated a favorable risk benefit ratio of empagliflozin as monotherapy8 as well as add-on therapy to other hypoglycemic agents.9,10,11,12 They also have additional cardiovascular benefits with several studies documenting a reduction in mortality.13,14 Moreover, the sodium glucose co-transporters also demonstrated a reduction in the onset and worsening of nephropathy and preservation of renal function.15 This effect is not restricted to empagliflozin alone, as other drugs in the class have also demonstrated this benefit.16 Empagliflozin with its novel mechanism of action has its own set of side effects. Increased urinary glucose losses lead to a higher proportion of urinary tract infections and genital tract infections. This has been evidenced in various studies.17 The osmotic diuresis that benefits in lowering blood pressures at one end, also predisposes the patients to volume depletion.Empagliflozin, one of the three drugs from this class, approved by the FDA for treatment of type 2 diabetes. According to the recent ADA and the EASD guidelines, they have become an essential component of the algorithm recommended for managing type 2 diabetes.18 The recently published consensus statement by the South Asian Federation of Endocrine Societies has incorporated sodium glucose co-transporter 2 inhibitors in the treatment of patients with type 2 diabetes as monotherapy in patients who are intolerant to or have any contraindication to metformin therapy. Additionally, drugs belonging to this class are also recommended as combination therapy with other oral hypoglycemic agents as well as insulin.19 Empagliflozin, however, has not been studied in the Pakistani population as yet. The main aim of this study is to establish the efficacy and safety of empagliflozin in optimum control of blood sugar in type 2 diabetes. This is the first study of its kind being performed in the Pakistani population.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
244 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Empagliflozin
Arm Type
Experimental
Arm Title
Usual Care Group
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Empagliflozin
Other Intervention Name(s)
Group A
Intervention Description
Group A: Empagliflozin 10/25 mg once daily with or without antidiabetic drugs
Intervention Type
Drug
Intervention Name(s)
Usual care group
Other Intervention Name(s)
Group B
Intervention Description
Group B: usual care group but without Empagliflozin with adjustment of therapy as the standard of care
Primary Outcome Measure Information:
Title
Number of participants reported adverse events
Description
Number of participants reported adverse events such as Hypoglycemic events, Hypotension, Dehydration, Urinary tract infection, Diabetic Ketoacidosis, Fungal infection or any other
Time Frame
24 weeks
Secondary Outcome Measure Information:
Title
Frequency of participants achieved HbA1c level <7%
Description
Frequency of participants achieved HbA1c level <7%
Time Frame
24 weeks
Title
Frequency of participants achieved FBS level within normal range
Description
Frequency of participants achieved FBS level within normal range
Time Frame
24 weeks
Other Pre-specified Outcome Measures:
Title
Number of participants reduces weight during the therapy
Description
Number of participants reduces weight during the therapy or mean reduction in weight overtime
Time Frame
24 weeks
Title
Number of participants reduces BMI level as per WHO Asian classification during the therapy
Description
Number of participants reduces BMI or mean reduction in BMI overtime
Time Frame
24 weeks
Title
Number of participants reduces Waist circumference during the therapy
Description
Number of participants reduces Waist circumference or mean reduction in BMI overtime
Time Frame
24 weeks
Title
Number of participants changes systolic blood pressure and diastolic blood pressure during the therapy
Description
Number of participants reduces systolic blood pressure and diastolic blood pressure or mean reduction in systolic blood pressure and diastolic blood pressure overtime
Time Frame
24 weeks
Title
Number of participants changes LDL level and HDL Level during the therapy
Description
Number of participants reduces LDL level and HDL Level or mean reduction in LDL level and HDL Level overtime
Time Frame
24 weeks
Title
Mean score of diabetes mellitus quality of life
Description
The instrument provides an overall scale score, as well as two subscale scores for 1) satisfaction with treatment, 2) adherence with Self Care Regimen. 15 Items are scored on a 5-point Likert scale and are of two general formats.One format asks about the frequency of negative impact of diabetes itself or of the diabetes treatment and provides response options from 1 (never) to 5 (all the time). The second format asks about satisfaction with treatment and quality of life and is scored from 1 (very satisfied) to 5 (very dissatisfied). Higher scores on DQOL items and subscales are, therefore, negatively valenced, indicating problem frequency or dissatisfaction.
Time Frame
24 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Pakistani muslim male / female, type 2 diabetic patient having age from 18 years to 75 years Patient who give informed consent voluntarily BMI ≤45 kg/m2 Glycosylated hemoglobin of 7 - ≤10% Exclusion Criteria: Patients who are on empagliflozin treatment Indication of liver disease, defined by serum levels of either alanine aminotransferase, aspartate aminotransferase, and alkaline phosphatase above 3 times upper limit to normal Estimated glomerular filtration rate (eGFR) <45 mL /min /1.73m2 History of recurrent urinary tract infection (UTI) and/or past 3 months' history of UTI and its treatment Patients with positive urine culture for UTI at the time of screening Patients who have been admitted to the hospital in the past 3 months for diabetic ketoacidosis (DKA) and hyperosmolar hyperglycemic state Patients with past 3 months' history of fungal infection and its treatment History of blood dyscrasias or any disorders causing haemolysis or unstable red blood cell History of benign prostate hyperplasia Any acute coronary syndrome, stroke and/or transient ischemic attack (TIA) in the previous 3 months Any contraindication for patients to Biguanides, Sulfonylureas, DPP-IV inhibitors, SGLT-2 Inhibitors Treatment with anti-obesity drugs or any other treatment leading to unstable body weight Patients with past 6 weeks treatment history with systemic steroids or thyroid hormones or any other uncontrolled endocrine disorder except T2DM Pre-menopausal women who are nursing or pregnant or are of childbearing potential and not practicing an acceptable method of birth control Any other clinical condition that would jeopardize patients safety while participating in this study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
A H Aamir
Organizational Affiliation
Post Graduate Medical Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Balochistan Medical Center
City
Quetta
State/Province
Balochistan
Country
Pakistan
Facility Name
Lady Reading Hospital
City
Peshawar
State/Province
Khyber Pakhtunkhwa
Country
Pakistan
Facility Name
Post Graduate Medical Institute
City
Peshawar
State/Province
Khyber Pakhtunkhwa
Country
Pakistan
Facility Name
Hanif Medical Center
City
Islamabad
State/Province
Punjab
Country
Pakistan
Facility Name
Shifa International Hospital
City
Islamabad
State/Province
Punjab
Country
Pakistan
Facility Name
Diabetes Institute of Pakistan
City
Lahore
State/Province
Punjab
Country
Pakistan
Facility Name
Jinnah Hospital
City
Lahore
State/Province
Punjab
Country
Pakistan
Facility Name
National Defence Center
City
Lahore
State/Province
Punjab
Country
Pakistan
Facility Name
Al-Khaliq Hospital
City
Multān
State/Province
Punjab
Country
Pakistan
Facility Name
Fatimiyah Hospital
City
Karachi
State/Province
Sindh
Country
Pakistan
Facility Name
National Institute of Cardiovascular Disease
City
Karachi
State/Province
Sindh
Country
Pakistan

12. IPD Sharing Statement

Plan to Share IPD
No

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Safety And Efficacy Of Empagliflozin In Pakistani Muslim Population With Type Ii Diabetes Mellitus

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