Ireland
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Recruiting Phase 3

A Trial to Evaluate the Efficacy of Pioglitazone to Promote Renal Tolerance in ANCA-associated Vasculitis - RENATO Trial

NCT05946564 · tracked via the Priya Life Science France tracker
Phase
Phase 3
Started
2023-10-24
Last updated
2026-07-01

Condition(s) studied

ANCA Associated VasculitisRapidly Progressive GlomerulonephritisCrescentic Glomerulonephritis

Investigational drug(s) / intervention(s)

Pioglitazone (ACTOS®) →Placebo of Pioglitazone

Pioglitazone (ACTOS®): Patient will be randomize in the intervention group receive treatment by pioglitazone (30 mg/day orally) for 26 weeks on top of a SOC immunosuppressive treatment.

Placebo of Pioglitazone: Patient will be randomize in the intervention group receive treatment by placebo of pioglitazone (30 mg/day orally) for 26 weeks on top of a SOC immunosuppressive treatment.

Study summary

The RENATO trial is a multicenter randomized controlled trial that evaluates the efficacy of pioglitazone to improve renal outcomes in ANCA-associated vasculitis.

Patients with biopsy-proven kidney involvement of ANCA vasculitis will be included in this trial at diagnosis. All patients will receive a standard of care immunosuppressive (SOC) therapy combining corticosteroids and rituximab (375 mg/m2/week for 4 consecutive weals followed by 500 mg re-infusion every 6 months). They will be randomized 1:1 to receive either pioglitazone 30 mg/day or placebo for 6 months, on top of SOC. The primary objective of this trial is to demonstrate that pioglitazone reduces kidney damage, reflected by the early improvement of proteinuria and serum creatinine levels. The secondary objectives will be to assess the efficacy of this drug on the reduction of hypertension and metabolic effects of glucocorticoids, to measure its impact on vasculitis activity and to evaluate the safety profile of pioglitazone in this population.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * Newly-diagnosed or relapsing ANCA-associated vasculitis, i.e. granulomatosis with polyangitis (GPA) or microscopic polyangiitis (MPA), according to ACR 1990 criteria and/or revised Chapel Hill Consensus Conference definitions and/or European Medical Agency algorithm, with an active disease defined as a BVAS ≥3 * Presence of proteinuria (UPCR \>300 mg/g), haematuria (\>10 RBC/hpf), and eGFR ≥15 mL/min/1.73 m2 (CKD-EPI formula) at inclusion (\<1 month) * Recent (\<4 weeks) renal biopsy that confirms active renal involvement of ANCA-associated vasculitis * Patients aged of 18 to 80 years * Participant written informed consent prior to participation in the study * Participants affiliated to a French health insurance system (registered or being a beneficiary of such a scheme) Exclusion Criteria: * Alveolar haemorrhage requiring pulmonary ventilation support at inclusion * Patients with eosinophilic granulomatosis with polyangiitis (EGPA, Churg-Strauss) * Active cancer (except non-melanoma skin cancer) within the past 24 months * Active severe bacterial, viral or fungal infectious disease * Past history of bladder or urinary tract cancer * History of Class 3/4 congestive heart failure symptoms, any time * History of Class 2 heart failure symptoms within the past 3 months and/or ejection fraction \<40% on recent echocardiography (\<1 month) * Transaminases levels above 2 times the normal range value (\<1 month) or any severe chronic liver disease * Positive serology for HIV, HBV (Ag HBs positivity) or active HCV infection at inclusion * Presence of neutropenia \<1000 cells/l (\<1 month) * History of intolerance to any thiazolidinedione (including Pioglitazone), to rituximab or any excipient listed in SmPc * Diabetic ketoacidosis, any time * A pre-existing or an important risk of new-onset macular edema (confirmed by an ophthalmological examination) * Pregnant or breast-feeding women, or desire to become pregnant within 24 months All women of childbearing potential (WOCBP) are required to have a negative pregnancy test before treatment and must agree to maintain highly effective contraception by practicing abstinence or by using an effective method of birth control from the date of consent through the end of the study and another 12 months after (or 12 months after the last rituximab infusion in case of premature termination): Combined (estrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation (Oral, Intravaginal, Transdermal); Progestogen-only hormonal contraception associated with inhibition of ovulation (Oral, Injectable, Implantable); Intrauterine device (IUD); Intrauterine hormone-releasing system (IUS); Bilateral tubal occlusion; Vasectomised partner * Severe neurologic or psychiatric disease (e.g., dementia or schizophrenia) * Kidney transplant recipients * Cyclophosphamide or rituximab (dose \> 375 mg/m2) use within 26 weeks prior to screening; if on azathioprine, mycophenolate mofetil or methotrexate at the time of screening, these drugs must be withdrawn prior to receiving the first rituximab dose. Patients that have initiated induction therapy with rituximab for the actual flare, can be included in the present study within 48h following the first rituximab infusion * Intravenous glucocorticoids, \>3000 mg methylprednisolone equivalent, within 4 weeks prior to screening * Patients who have been taking an oral daily dose of a glucocorticoid of more than 10 mg prednisone-equivalent for more than 6 weeks continuously prior to screening * Current participation in another research study involving a therapeutic intervention. Participation to an observational research, or a non-interventional research is allowed * Patients under guardianship or curators and protected adults * Patients not able to understand and follow study procedures * Patients on AME (Aide Médicale de l'Etat = State Medical Assistance)

Primary outcome measure(s)

  • Appearance of a success defined as (1) Delta sCreat > 30% (between D0 and week 26) AND (2) urine protein-to-creatinine (uPCR) < 1g/mmol — Week 26

Trial sites (25)

FacilityCityRegionStatus
CHU Amiens Amiens France Recruiting
CHU d'Angers Angers France Recruiting
CH de Boulogne sur Mer Boulogne-sur-Mer France Recruiting
CHU Brest - Hôpital de la Cavale Blanche Brest France Recruiting
CHU de Dijon Dijon France Recruiting
CHU de Grenoble - Hôpital Michalon site nord Grenoble France Recruiting
Centre Hospitalier Départemental Vendée La Roche-sur-Yon France Recruiting
Hopital Le Kremlin Bicetre - Aphp Le Kremlin-Bicêtre France Recruiting
AP-HM - Hôpital la Conception Marseille France Recruiting
CHU de Nantes - Hotel Dieu Nantes France Recruiting
CHU Pasteur 2 - Nice Nice France Recruiting
CHU Nîmes - Hôpital universitaire Caremeau Nîmes France Recruiting
AP-HP - Hôpital Cochin Paris France Recruiting
AP-HP - Necker enfants malades Paris France Recruiting
HEGP Paris France Recruiting
AP-HP - Hôpital Bichat Paris France Recruiting
AP-HP - Tenon Paris France Recruiting
AP-HP - Henri Mondor Paris France Recruiting
AP-HP - Hôpital Ambroise-Paré Paris France Recruiting
CHU de Rouen Rouen France Recruiting
CHU de Strasbourg Strasbourg France Recruiting
CHU de Toulouse - Hôpital Rangueil Toulouse France Recruiting
CH Valenciennes Valenciennes France Recruiting
Chru de Nancy Vandœuvre-lès-Nancy France Recruiting
Hôpital Robert Schuman (UNEOS) Vantoux France Not Yet Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05946564 on ClinicalTrials.gov ↗ ← All trials in France