Dapagliflozin in Non-diabetic Stage IV CKD

Chronic Kidney Diseases Clinical Trial

— ADAPT  

Official title:

Evaluating the Short-term Renal and Systemic Effects of Dapagliflozin in Non-diabetic Patients With Stage IV CKD at Risk of ESKD Because of Severe Renal Insufficiency and Persistent Proteinuria: A Prospective, Randomized, Double-blind, Placebo-controlled, Cross-over Study

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT04794517
• Other study ID #: ADAPT
• Secondary ID: 2021-000726-10
• Status: Active, not recruiting
• Phase: Phase 2
• Start date: November 8, 2021
• Est. completion date: May 2024

Study information

• Verified date: December 2023
• Source: Mario Negri Institute for Pharmacological Research
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

As chronic kidney disease (CKD) continues to increase worldwide, along with the demand for related life-saving therapies, the financial burden of CKD will place an increasing drain on health care systems. Experimental studies showed that glomerular capillary hypertension and impaired sieving function with consequent protein overload play a pathogenic role in the progression of CKD. Consistently, human studies show that proteinuria is an independent predictor of progression and that its reduction is renoprotective. At comparable BP control, inhibitors of the renin-angiotensin system (RAS), including angiotensin converting enzyme (ACE) inhibitors and angiotensin II receptor blockers (ARBs), more effectively than non-RAS inhibitor therapy reduce proteinuria, slow progression to ESRD, and even improve the kidney function achieving disease regression in some cases. In participants with diabetes, RAS inhibitors delay the onset of microalbuminuria and its progression to macroalbuminuria, and ACE inhibitors may reduce the excess cardiovascular mortality associated with diabetic renal disease. In addition to RAS inhibitors, however, multimodal approaches including lifestyle modifications and multidrug therapy will be required in most cases to optimize control of the several risk factors for CKD and related cardiovascular morbidity. Novel medications, including proximal tubular sodium - glucose co-transporter -2 (SGLT2 inhibitors - that ameliorate glomerular hyperfiltration and proteinuria and slow renal disease progression in type 2 diabetes by mechanisms apparently independent of improved metabolic control - might help further improve the cost-effectiveness of renoprotective interventions even in non-diabetic CKD. This phase 2, prospective, randomized, cross over, placebo-controlled trial will primarily aim to assess whether the SGLT2 inhibitor dapagliflozin ameliorates hyperfiltration and reduces proteinuria as compared to placebo in patients with non-diabetic CKD, with particular focus on those at highest risk of progression to end stage kidney disease (ESKD) because of severe renal insufficiency (Stage IV CKD) and proteinuria (>0.5 g/24 hours).

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 32
• Est. completion date: May 2024
• Est. primary completion date: May 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Provision of informed consent prior to any study specific procedures

2. Male or female more than 18 year old

3. Non-diabetic Stage-IV CKD

4. Fasting blood glucose = 125 mg (= 6.9 mmol/l) and HbA1C =6.4% (= 47 mmol/mol)58 without treatment with oral blood glucose lowering medications and/or insulin

5. Two-hour plasma glucose <200 mg/dl during 75-g oral glucose tolerance test (OGTT)58

6. Persistent proteinuria (24-hour urinary protein excretion = 0.5 grams in at least two consecutive evaluations >1 week apart) despite RAS inhibitor therapy with ACE inhibitors and/or ARBs (or without RAS inhibitors in patients with specific contraindications to these medications)

7. eGFR 15 to 30 ml/min/1.73 m2 by CKD-Epi equation

8. Blood pressure <150/90 mmHg without changes in blood pressure lowering medications over the last four weeks before the randomization

9. Negative pregnancy test (urine or serum) for female subjects of childbearing potential.10

10. Female subjects must be 1 year post-menopausal, surgically sterile, or using an acceptable method of contraception (an acceptable method of contraception is defined as a barrier method in conjunction with a spermicide) for the duration of the study (from the time they sign consent) and for 3 months after the last dose of dapagliflozin\placebo to prevent pregnancy. In addition, oral contraceptives, approved contraceptive implant, long-term injectable contraception, intrauterine device, or tubal ligation are allowed. Oral contraception alone is not acceptable; additional barrier methods in conjunction with spermicide must be used.

11. Male subjects must be surgically sterile or using an acceptable method of contraception (defined as barrier methods in conjunction with spermicides) for the duration of the study (from the time they sign consent) and for 3 months after the last dose of IMP to prevent pregnancy in a partner.

12. Subjects who are blood donors should not donate blood during the study and for 3 months following their last dose of dapagliflozin\placebo.

Exclusion Criteria:

1. Involvement in the planning and/or conduct of the study (applies to both Investigator staff and/or staff at the study site)

2. Participation in another clinical study with an investigational product during the last month

3. Ischemic kidney disease (because of possible excess risk of acute kidney injury upon SGLT2-inhibitor associated reduction in sodium pool and kidney perfusion pressure)

4. Rapidly progressive kidney disease (e GFR reduction = 30% over the last three months) and expected risk of progression to end stage kidney failure and need of renal replacement therapy by dialysis or transplantation during the study period.

5. Active systemic autoimmune diseases;

6. Concomitant treatment with steroids or any other immunosuppressive agent

7. Hypersensitivity to the active principle (dapagliflozin) or any of the excipients (e.g. lactose);

8. Severe/unstable heart failure with or without decreased systolic function requiring hospitalization or changes in pharmacological therapy over the last three months

9. Uncontrolled hypertension (BP >150/90 mmHg despite optimized pharmacological treatment and diet or symptomatic hypotension

10. Positive hepatitis C antibody hepatitis B virus surface antigen or hepatitis B virus core antibody, at screening

11. Known to have tested positive for human immunodeficiency virus

12. Drug or alcohol abuse

13. Inability to fully understand the possible risks and benefits related to study participation

14. If female, the subject is pregnant or lactating or intending to become pregnant before, during, or within 90 days after last dose; or intending to donate ova during such time period;

15. If male, the subject intends to donate sperm while on the study this study or for 90 days after last dose;

16. Participation in another interventional clinical trial within the 4 weeks prior to screening.

Related Conditions & MeSH terms

• Chronic Kidney Diseases
• Kidney Diseases
• Renal Insufficiency, Chronic

Intervention

Drug:
• Dapagliflozin 10Mg Tab
Dapagliflozin 10 mg/die will be administered orally for six-weeks.

Other:
• Placebo
Placebo one tablet/die will be administered orally for six-weeks.

Locations

Country	Name	City	State
Italy	Centro di Ricerche Cliniche per le Malattie Rare "Aldo e Cele Daccò"	Ranica	BG

Sponsors (2)

Lead Sponsor	Collaborator
Mario Negri Institute for Pharmacological Research	AstraZeneca

Country where clinical trial is conducted

Italy, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Glomerular Filtration rate (GFR)	GFR measured by the Iohexol plasma clearance technique	Changes from baseline and day 1, 8, 42,84, 92,126 and 140.
Primary	24-hour urinary protein excretion	24-hour urinary protein excretion will be measured as median of three measurements in three consecutive 24-hour urine collections	Changes from start (day 0, day 84) and end (day 42, day 126) of each Treatment Period with dapagliflozin or placebo
Secondary	Renal plasma flow (RPF)	RPF will be assessed by the Para Amino Hippuric (PAH) plasma clearance technique.	Changes from baseline and day 1, 8, 42,84, 92,126 and 140.