Phase
Condition
Nephropathy
Hypertriglyceridemia
Diabetes And Hypertension
Treatment
Finerenone (Kerendia, BAY94-8862)
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Participants capable of giving signed informed consent signed before anystudy-specific procedure and willing to comply with the study-related procedures.
Diagnosis of chronic kidney disease (CKD) associated with type 2 diabetes (T2D).
Participants who are drug naïve for finerenone or patients who have been initiatedon finerenone therapy within 4 weeks before signing the informed consent.
Participants with serum potassium level ≤ 4.8 mmol/L at the time of Screening. Ifserum potassium level > 4.8 to 5.0 mmol/L, participants may be enrolled in thestudy, but additional potassium samples may be required; the potassium level needsto be confirmed during Screening. Participants with potassium level > 5.0 mmol/L arenot allowed. The sample for potassium assessment for confirming eligibility shall beavailable before initiation of treatment with finerenone.
Contraceptive use by women should be consistent with local regulations regarding themethods of contraception for those participating in clinical studies.
Exclusion
Exclusion Criteria:
- Contraindications according to the local marketing authorization:
Participants with eGFR < 25 mL/min/1.73 m^2 (calculated based on the CKD-EPIequation, using 2009 formula). eGFR can be reassessed once within 48 hours.
Participants with severe hepatic impairment (Child-Pugh C).
Participants with known hypersensitivity to the study treatment (activesubstance or excipients).
Participants with Type 1 Diabetes.
Participants taking concomitant medications that are strong CYP3A4 inhibitors.
Participants with Addison's disease.
Glycated hemoglobin > 12% (17.5 mmol/L) at the Screening visit.
Participants treated with another mineralocorticoid receptor antagonist (MRA), arenin inhibitor, potassium supplements, a potassium sparing diuretic, a potassiumbinder agent, or angiotensin receptor neprilysin inhibitor (ARNI) within 8 weeksprior to the Screening visit and during finerenone treatment.
Participation in another interventional clinical trial within 30 days prior to theScreening visit and during finerenone treatment.
Female participants who are pregnant or breast-feeding or plan to become pregnant orto breastfeed during the course of the study.
Participants known for lack of compliance with clinic visits or prescribedmedication.
Study Design
Connect with a study center
Bhate Hospital
Karnataka, Belagavi 590002
IndiaSite Not Available
All India Institute of Medical Sciences
New Delhi, Delhi 110029
IndiaActive - Recruiting
PSRI Institute of Renal Sciences
New Delhi, Delhi 110017
IndiaSite Not Available
Vardhman Mahavir Medical College & Safdarjung Hospital
New Delhi, Delhi 110029
IndiaActive - Recruiting
Vardhman Mahavir Medical College & Safdarjung Hospital (VMMC-SJH)
New Delhi, Delhi 110029
IndiaSite Not Available
Muljibhai Patel Urological Hospital
Nadiad, Gujarat 387001
IndiaActive - Recruiting
Muljibhai Patel Urological Hospital (MPUH) (Kidney Hospital)
Nadiad, Gujarat 387001
IndiaSite Not Available
Accord Superspeciality Hospital
Faridabad, Haryana 121002
IndiaSite Not Available
Kempegowda Institute of Medical Sciences Hospital & R C
Bangalore, Karnataka 560004
IndiaSite Not Available
Christian Medical College
Vellore, Kerala 632004
IndiaSite Not Available
Global Hospital-Super Speciality And Transplant Centre
Mumbai, Maharashtra 400012
IndiaSite Not Available
Lancelot Medical Centre
Mumbai, Maharashtra 400092
IndiaSite Not Available
Dr Balabhai Nanavati Hospital
Mumbai, Maharashtra,, Maharashtra 400056
IndiaSite Not Available
All India Institute of Medical Sciences
Bhubaneswar, Odisha 751019
IndiaSite Not Available
Jawaharlal Institute Of Postgraduate Medical Education and R
Gorimedu, Pondicherry 605006
IndiaSite Not Available
Government Stanley Medical College & Hospital
Chennai, Tamil Nadu 600001
IndiaActive - Recruiting
Government Stanley Medical College and Hospital
Chennai, Tamil Nadu 600001
IndiaSite Not Available
M.V. Hospital & Research Centre 314/30
Chowk Lucknow, Uttar Pradesh 226003
IndiaSite Not Available
Sanjay Gandhi Post Graduate Institute of Medical Sciences
Lucknow, Uttar Pradesh 226 014
IndiaActive - Recruiting
Sanjay Gandhi Postgraduate Institute of Medical Sciences (SGPGIMS)
Lucknow, Uttar Pradesh 226 014
IndiaSite Not Available
Medica Superspecialty Hospital
Kolkata, West Bengal 700099
IndiaSite Not Available
Nizam's Institute of Medical Sciences
Hyderabad, 500082
IndiaActive - Recruiting
Nizam's Institute of Medical Sciences (NIMS)
Hyderabad, 500082
IndiaSite Not Available
Many Locations
Multiple Locations,
IndiaSite Not Available
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