Treatment of Lupus Nephritis With Allogeneic Mesenchymal Stem Cells

A vizsgálat adatai

Ki végzi

Red de Terapia Celular

Azonosító

NCT03673748EU 2024-514750-67-00

A regiszteradat frissítve

2026. augusztus 18.

Eredeti leírás

The purpose of this study is to evaluate the safety and efficacy of mesenchymal stem cells (MSCs) obtained from bone marrow for the treatment of adults with active proliferative lupus nephritis. The objective of this study is to evaluate the efficacy of mesenchymal stem cells (MSCs) in achieving a full or partial response in the treatment of Lupus Nephritis (LN) during its induction period.A teljes eredeti leírásKevesebb

Phase II, Double-Blind, Placebo-Controlled Clinical Trial to Evaluate Safety and Efficacy of Mesenchymal Stem Cells (MSV-allo) in the Treatment of Lupus Nephritis

The purpose of this study is to evaluate the safety and efficacy of mesenchymal stem cells (MSCs) obtained from bone marrow for the treatment of adults with active proliferative lupus nephritis. The objective of this study is to evaluate the efficacy of mesenchymal stem cells (MSCs) in achieving a full or partial response in the treatment of Lupus Nephritis (LN) during its induction period.

Bevonási feltételek: Females or males ≥18 years old who provide written informed consent at the selection visit; Diagnosis of systemic lupus erythematosus (SLE) by meeting at least 4 of the 11 criteria included in the American College of Rheumatology (ACR) classification and/or the Systemic Lupus International Collaborating Clinics (SLICC) criteria, at the selection visit; Diagnosis of lupus nephritis (LN) using the 2003 classification of the International Society of Nephrology and the Society of Renal Pathology, by biopsy performed no more than 6 months before the selection visit if they enter from the induction period, and no more than one year if they enter with a moderate/severe recurrence; No response or partial response to standard treatment, or moderate/severe recurrence of lupus nephritis; SLEDAI-2K ≥ 10 during the selection period; Women of childbearing potential should use effective methods of contraception to prevent pregnancy; Have been vaccinated against pneumococcus and influenza at the time the vaccination campaign is carried out.

Kizáró feltételek: A - Related to previous treatments:; Use of rituximab, belimumab, ocrelizumab or other biologic therapies against B cells in the 6 months prior to selection; Use of cyclophosphamide in the 6 months prior to selection; Use of any tumor necrosis factor inhibitor treatment in the 6 months prior to selection; Use of immunoglobulins in the 6 months prior to selection; Change in doses of an angiotensin converting enzyme inhibitor or an angiotensin receptor inhibitor in the two months prior to selection; Treatment with another investigational medicinal product within three months prior to selection or 5 times the half-life of the agent; B - Related to medical problems:; Cardiac, peripheral, or cerebrovascular cardiovascular events in the 6 months prior to the selection visit; Thromboembolic events in the 12 months prior to or during selection, whether or not associated with associated antiphospholipid syndrome, or inadequate anticoagulation tests 6 weeks immediately prior to or during selection visit; Active central nervous system SLE that is considered severe or progressive (recent uncontrolled seizures, changes in anticonvulsant treatment within 3 months prior to selection visit, or resulting in significant cognitive impairment); Comorbidities that require treatment with systemic corticosteroids (oral, rectal or injectable) such as asthma or inflammatory bowel disease; Antecedents or plans for an organ transplant; Clinically significant active viral, bacterial or fungal infection, or having suffered a major episode of infection that required hospitalization or parenteral treatment in the 4 weeks prior to the selection visit, during the selection visit, or having finished anti-infective treatment within 2 weeks prior to or during selection, or a history of recurrent infections (three or more cases of the same type of infection in a consecutive 12-month period). Controlled vaginal candidiasis, onychomycosis, and genital or oral herpes simplex virus would not be reasons for exclusion; Diagnosis of active or latent tuberculosis (TB) using a purified protein derivative TB skin test (induration ≥ 5 mm) or a positive Quantiferon test result, at selection or within 3 months prior to the selection visit. Patients who have completed previous adequate treatment or who are receiving treatment will not repeat the test. Patients who are receiving adequate TB treatment for at least 4 continuous weeks prior to the selection visit and who are expected to complete the treatment regimen will not be excluded; Major surgical intervention within 6 weeks prior to selection visit or planned during the trial period, including follow-up; Chest X-ray with significant changes indicating active TB. The chest X-ray must have been performed within 3 months prior to the selection visit or during the selection period; D - Others:; Use of corticosteroids or mycophenolate above the doses allowed for induction, according to the Consensus Document of the Systemic Autoimmune Diseases Group of the Spanish Society of Internal Medicine and the Spanish Society of Nephrology; Any pathology, including an uncontrolled disease other than SLE, which, in the opinion of the investigator, the sponsor or the person they designate, constitutes an inappropriate risk or a contraindication for participation in the trial or that could interfere with the objectives of the trial, its performance or evaluation; Active cardiac arrhythmia or clinically significant electrocardiogram abnormalities at selection visit or on the day of randomization that, in the opinion of the investigator, sponsor, or designee, constitute an inappropriate risk or contraindication to participation in the study; History or current diagnosis of a demyelinating disease such as multiple sclerosis or optic neuritis; History of or positive human immunodeficiency virus (HIV) test result, hepatitis C antibodies and/or detection by polymerase chain reaction, hepatitis B surface antigen (HBsAg+), and/or IgM or total antibodies against hepatitis B nuclear antigen at selection; Presence of class 3 or 4 uncontrolled congestive heart failure according to the New York Heart Association; Active cancer; Pregnant or lactating women; C - Laboratory abnormalities:; Clinically significant laboratory test abnormalities not attributed to active SLE; Legal incapacity.

ClinicalTrials.gov NCT03673748 · EU CTIS 2024-514750-67-00