Albuminuria Reduction Trial and Investigation with Survodutide Treatment in CKD (ARTIST-CKD)

Trial details

Who runs it

Universitair Medisch Centrum Groningen

Trial code

EU 2025-525068-13-00

Record updated

2026. május 19.

Original description

The primary objective of the ARTIST-CKD trial is to evaluate the effect of survodutide 3.6 mg per week on albuminuria in people with CKD, irrespective of the presence or absence of diabetes.Read full original descriptionShow less

The primary objective of the ARTIST-CKD trial is to evaluate the effect of survodutide 3.6 mg per week on albuminuria in people with CKD, irrespective of the presence or absence of diabetes.

Inclusion: Age ≥ 18 years; eGFR ≥ 20 and <90 mL/min/1.73m2; Urinary albumin to creatinine ratio ≥30 mg/g and <3500 mg/g; BMI ≥ 23 kg/m2 (with participants with BMI ≥23 to <25 capped at 10% of the total study population); Stable kidney function (no more than 30% change in eGFR in the 3 months prior to enrolment); On a stable maximum tolerated dose of an ACEi/ARB for at least 4 weeks prior to enrolment; If using an SGLT2 inhibitor, receiving a stable dose for at least 8 weeks prior to enrolment; Willing to sign an informed consent; If using an MRA, receiving a stable dose for at least 8 weeks prior to enrolment.

Exclusion: Donation or loss of ≧400 ml blood within 8 weeks prior to initial dosing; Cardiovascular event within 3 months prior to enrolment; Treatment with GLP-1RA for <12 weeks prior to screening; Participation in any clinical trial within 3 months prior to initial dosing; Diagnosis of type 1 diabetes; History of chronic pancreatitis or idiopathic acute pancreatitis; History of noncompliance to medical regimens or unwillingness to comply with the study protocol; Any surgical or medical condition, which in the opinion of the investigator, may place the patient at higher risk from his/her participation in the study, or is likely to prevent the patient from complying with the requirements of the study or completing the study; Personal or family history of multiple endocrine neoplasia type 2 (MEN2) or familial medullary thyroid carcinoma; Personal history of non-familial medullary thyroid carcinoma; History of severe hypersensitivity or contraindications to any glucagon RA or GLP-1 RA; Uncontrolled arterial hypertension (mean semi supine systolic blood pressure (SBP) ≥180 mmHg or diastolic blood pressure (DBP) ≥110 mmHg); Additional criteria applicable for sub-set of participants for MRI assessment of perirenal, epicardial, subcutaneous and visceral fat: o Contraindication to MRI including, but not limited to severe claustrophobia, extensive tattoos, inner ear implant, pacemakers incompatible with MRI, other implanted cardiac rhythm management device, intracranial aneurism clips incompatible with MRI, any other metallic, non-MRI compatible implanted devices (e.g. hip replacement), a history of intra-orbital metal fragments that have not been removed, and weight or girth that exceeds scanner capabilities o Participants who do not fulfil the MRI criteria are eligible for the main trial if the eligibility criteria for the main trial are fulfilled; History of kidney or liver transplant; Active malignancy; Suggestive evidence of adrenal insufficiency; A history of acute pancreatitis; Any medication, surgical or medical condition which might significantly alter the absorption, distribution, metabolism, or excretion of medications including, but not limited to any of the following: History of active inflammatory bowel disease within the 6 months; Major gastrointestinal tract surgery as determined by the physician; A history of pancreatitis; GI ulcers and/or bleeding within 6 months; Evidence of urinary obstruction or difficulty in voiding at screening; History of drug or alcohol abuse within the 12 months prior to dosing, or evidence of such abuse as indicated by the laboratory assays conducted during the screening or according to investigator’s assessment; Women of childbearing potential (WOCBP): WOCBP who are unwilling or unable to use an acceptable method of contraception to avoid pregnancy throughout the study and for up to 8 weeks after the last dose of study drug in such a manner the risk of pregnancy is minimized; WOCBP without a negative serum or urine pregnancy test result (minimum sensitivity 25 IU/L or equivalent of HCG) at screening; Evidence of severe hepatic impairment determined by any one of: ALT or AST values exceeding 3x ULN, a history of hepatic encephalopathy, a history of oesophageal varices, or a history of portocaval shunt; Elevation of serum lipase (>3 x ULN); HbA1c > 10.5%; Vulnerable (i.e. under guardianship) or mentally incapacitated subjects (i.e. not able to understand and sign the informed consent); Calcitonin levels ≥100 pg/mL or 29.26 pmol/L; Use of sensitive CYP3A4 substrates with a narrow therapeutic index (e.g. alfentanil, fentanyl, carbamazepine, cyclosporine, tacrolimus, sirolimus) or use of any GLP-1, GIP/GLP-1 or GIP/GLP-1/glucagon receptor agonist; Uncontrolled unstable diabetic retinopathy or maculopathy; Active pregnancy or breastfeeding.

EU CTIS 2025-525068-13-00