A clinical study to assess the efficacy and safety of Dapagliflozin plus Telmisartan Tablets in kidney patients.

Phase 3

• Conditions: Health Condition 1: N189- Chronic kidney disease, unspecified

• Registration Number: CTRI/2024/01/061927
• Lead Sponsor: Exemed Pharmaceuticals

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 4 March 2024

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

1. Male or female patients aged 18 to 65 years (both inclusive).

2. Patients with estimated glomerular filtration rate (eGFR) more than 30 mL per min per 1.73 m2 and less than 90 mL min per 1.73 m2 (using the CKD-EPI formula) for more than 3 months and at screening visit.

3. Patients with evidence of increased albuminuria for 3 months or more before screening visit and urine albumin ?to ?creatinine ratio (UACR) more than or equal to 100 mg per g and less than or equal to 3500 mg per g at screening visit.

4. Patients with serum potassium levels less than or equal to 5 mmol per L at screening visit.

5. Patients who were on the highest dose of Telmisartan Tablets 80 mg for more than 4 weeks.

6. Women of childbearing potential (WOCBP) must be using an acceptable method of contraception to avoid pregnancy throughout the study. WOCBP must have a negative urine pregnancy test at screening or baseline visit.

7. Patient with ability to understand and provide written, signed and dated informed consent form, which must have been obtained prior to screening.

8. Patients willing to comply with all the protocol requirements.

Exclusion Criteria

1. Patients with a history of Type 1 diabetes mellitus or secondary diabetes mellitus or diabetes insipidus.

2. Patients with a history of metabolic acidosis or diabetic ketoacidosis.

3. Patients with autosomal dominant or autosomal recessive polycystic kidney disease, lupus nephritis or ANCA-associated vasculitis.

4. Patients who are receiving cytotoxic therapy, immunosuppressive therapy or other immunotherapy for primary or secondary renal disease within 6 months prior to enrolment.

5. Patients with a history of organ transplantation.

6. Patients with MI, unstable angina, stroke or transient ischemic attack (TIA) within 12 weeks prior to screening.

7. Patients with significant cardiovascular disease such as myocardial infarction, angina pectoris, percutanous transluminal coronary angioplasty, coronary artery bypass grafting, stroke, heart failure (NYHA I-IV) less than 6 months before screening.

8. Patients with Coronary revascularization (percutaneous coronary intervention [PCI] or coronary artery bypass grafting [CABG]) or valvular repair or replacement within 12 weeks prior to randomization or planned to undergo any of these operations after randomization.

9. Female patients who are pregnant or breast-feeding or expecting to conceive within the projected duration of the study.

10. Female patients who are of childbearing potential and who are neither surgically sterilized nor willing to use reliable contraceptive methods (like hormonal, barrier methods or intrauterine device).

11. Patients with type 2 diabetes mellitus whose diabetes has not been stable and controlled for the previous three months and with HbA1c value more than or equal to 8%.

12. Patients with clinically significant impaired hepatic function (SGOT & SGPT more than 3X the UNL and or Total bilirubin more than 2X the UNL) at screening.

13. Patients with uncontrolled hypertension with sitting systolic BP more than or equal to 160 mmHg and or diastolic BP more than or equal to 100 mmHg at screening.

14. Patients with a history of autonomic dysfunction (e.g., history of fainting or clinically significant orthostatic hypotension).

15. Patients with a history of amputations.

16. Patients with eGFR change more than 30% in the last six months before screening.

17. Patients suffering from severe urinary tract infections (e.g., urosepsis, pyelonephritis), necrotizing fasciitis of the Perineum (Fournier’s Gangrene), intravascular volume contraction and or female genital mycotic infections prior to 6 months from screening.

18. Patients with history of inflammatory bowel disease or intestinal ulcers or chronic enteric diseases related to digestion and absorption.

19. Patients with any abnormality on 12-lead ECG at screening that in the opinion of the investigator is clinically significant and is judged as potential risk for patient’s participation in the study.

20. Patients with a history of anaemia or haemoglobinopathy and or haemoglobin less than 10 g per dL for men; haemoglobin less than 9 g per dL for women at screening.

21. Patients with intolerance, contraindication or potential allergy or hypersensitivity to any of the ingredients of study medication.

22. Patients with known immunocompromised status.

23. Patients with a history of any malignancy.

24. Patients with known case of infection with hepatitis B, hepatitis

Study & Design

• Study Type: Interventional
• Study Design: Not specified