Accepts Healthy Volunteers
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An interventional clinical study is where participants are assigned to receive one or more interventions (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes.
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|Eligible Ages||18 Years and Over|
Inclusion Criteria:Patients eligible for inclusion in this study have to fulfil all of the following criteria: 1. Patient must be able to understand and communicate with the investigator and comply with the requirements of the study and must give a written, signed and dated informed consent before any study assessment is performed. 2. Male or non-pregnant, non-nursing female patients at least 18 years of age. Before randomization, a woman of childbearing potential must be on a highly effective method of birth control consistent with local regulations regarding the use of birth control methods for subjects participating in clinical studies: eg, established use of oral, injected or implanted hormonal methods of contraception associated with inhibition of ovulation; placement of an intrauterine device (IUD) or intrauterine system (IUS); male partner sterilization (the vasectomized partner should be the sole partner for that subject); true abstinence (when this is in line with the preferred and usual lifestyle of the subject). A woman of childbearing potential must have a negative serum (β-human chorionic gonadotropin [β-hCG]) at baseline before randomization. A woman must agree not to donate ovocytes for the purposes of assisted reproduction during the study and for 3 months after receiving the last dose of study agent. Note: If the childbearing potential changes after start of the study (eg, woman who is not heterosexually active becomes active, premenarchal woman experiences menarche) that woman must begin a highly effective method of birth control, as described above. A man who is sexually active with a woman of childbearing potential and has not had a vasectomy must agree to use a barrier method of birth control eg, either condom with spermicidal foam/gel/film/cream/suppository or partner with occlusive cap (diaphragm or cervical/vault caps) with spermicidal foam/gel/film/cream/suppository, and all men must also not donate sperm during the study and for 3 months after receiving the last dose of study agent The method of birth control will be clearly documented in patient file. 3. Patients with active PsA according to CASPAR criteria for ≥6 months, despite ≥3 months of csDMARD therapy, and ≥4 weeks of non-steroidal anti- inflammatory drugs (NSAIDs) therapy. 4. At least 1 swollen joint at screening or baseline (despite csDMARD therapy) with ability to perform a synovial biopsy at W0. 5. Patients with newly documented latent TB are eligible provided initiation of appropriate treatment. 6. Concomitant MTX or SSZ is permitted if started ≥3 months prior to study start and at a stable dose (≤25 mg/week for MTX and ≤ 3 g/day for SSZ) for ≥4 weeks. 7. Patients on MTX must be on stable folic acid supplementation before randomization. 8. Concomitant NSAIDs and oral corticosteroids (≤10 mg prednisone/day) are permitted if stable for at least 2 weeks. 9. Allowed concomitant medications are to remain stable through week 24. 10. Patients cannot have previously received any biologic agent 11. DMARDs other than MTX or sulfasalazine (SSZ) must be interrupted. DMARDs other than MTX are not allowed within 4 weeks prior to or during trial participation. A washout period needs to be considered. (8 weeks for leflunomide). 12. At least one joint (small or large) to biopsy in order to get synovial tissue. Small joints must have an US grey-scale score > 2 on Doppler
Exclusion Criteria:Patients fulfilling any of the following criteria are not eligible for inclusion in this study. 1. Contraindications for needle-arthroscopy such as joint replacement (in the affected knee or ankle joint) or anticoagulation. 2. Use of any investigational drug and/or devices within 4 weeks of baseline, or a period of 5 half-lives of the investigational drug, whichever is longer. 3. Conditions/situations such as: 1. Patients with conditions/concomitant diseases making them non evaluable for the primary endpoint 2. Impossibility to meet specific protocol requirements (e.g. blood sampling) 3. Patient is the Investigator or any sub-investigator, research assistant, pharmacist, study coordinator, other staff or relative thereof directly involved in the conduct of the protocol 4. Uncooperative or any condition that could make the patient potentially noncompliant to the study procedures 4. Any therapy by intra-articular injections (e.g. corticosteroid) within 4 weeks before baseline. 5. Any intramuscular corticosteroid injection within 2 weeks before baseline. 6. Prior treatment with a biologic agent. 7. A history of active tuberculosis (TB).
This trial id was obtained from ClinicalTrials.gov, a service of the U.S. National Institutes of Health, providing information on publicly and privately supported clinical studies of human participants with locations in all 50 States and in 196 countries.
Phase 1: Studies that emphasize safety and how the drug is metabolized and excreted in humans.
Phase 2: Studies that gather preliminary data on effectiveness (whether the drug works in people who have a certain disease or condition) and additional safety data.
Phase 3: Studies that gather more information about safety and effectiveness by studying different populations and different dosages and by using the drug in combination with other drugs.
Phase 4: Studies occurring after FDA has approved a drug for marketing, efficacy, or optimal use.
The sponsor is the organization or person who oversees the clinical study and is responsible for analyzing the study data.
|Cliniques universitaires Saint-Luc- Université Catholique de Louvain|
The person who is responsible for the scientific and technical direction of the entire clinical study.
|Adrien NZEUSSEU TOUKAP, MDDirk ELEWAUT, MD, PhD|
|Principal Investigator Affiliation||Cliniques universitaires Saint-Luc- Université Catholique de LouvainUniversity Hospital, Ghent|
Category of organization(s) involved as sponsor (and collaborator) supporting the trial.
The disease, disorder, syndrome, illness, or injury that is being studied.
1. STUDY SYNOPSIS 1.1 Rationale Psoriatic arthritis (PsA) is a chronic inflammatory disease, leading to impaired function, reduced quality of life, comorbidities and increased mortality. Fortunately, improved knowledge about disease mechanisms catalyzed rapid development of effective targeted therapies for this disease. PsA is a clinically heterogenous disease. Connections between clinical manifestations, disease activity, disease severity and entheseal/synovial molecular patterns are still not understood. In addition, although many treatments targeting different molecules or cytokines are now available, clinicians are still facing difficulties in the treatment choice, owing to the lack of reliable markers improving patients stratification. In the present project, we want to take advantage of our expertise in the field to compare global molecular profiles up- or down-regulated in synovitis of patients with PsA resistant to conventional synthetic disease modifying anti-rheumatic drugs (csDMARDs), before and after administration of targeted therapies, in order to identify molecular markers associated with response to therapy. This may allow us to move further towards precision medicine. 1.2 Aim of the study We intend to evaluate global transcriptomic effects of ustekinumab (IL-12/IL-23/p40 blocker) and guselkumab (IL-23/p19 blocker) in synovial biopsies from csDMARD-resistant, biologic-naive patients with PsA, obtained prior to and 24 weeks after initiation of therapy. In parallel, synovial biopsies will be obtained before and after initiation of adalimumab (a widely used TNFα blocker) to evaluate the different molecular pathways affected by the different drugs. In order to deliver, this project will be based on the use of an Affymetrix platform (GeneChip HGU133 Plus2.0 chips). We and others amply demonstrated the power of this analytical approach in identifying synovial pathways associated with disease activity and response to therapy in the past (resulting in the development of a diagnostic and theranostic commercial kit). However, the material collected throughout the study will be a unique opportunity to carry out a more exploratory single cell RNASeq procedure on our samples, thereby potentially unravelling molecular effects of therapies in specific cell populations. Identification of the synovial effects of those treatments in psoriatic arthritis will be a step forward in understanding not only the mode of action of the drug at the site of inflammation, but also in the identification of molecular patterns associated with good response to therapy. The main advantage of our approach compared to other biomarker studies, is that we use synovial material as such, and not peripheral blood, which is a more remote location in terms of cellular targets of the drug. This project takes advantage of our strong experience in the field of molecular profiling of synovial biopsies, and evaluation of responses to biological agents. Key to the success of our translational approach is the association of reliable molecular techniques with a well-validated clinical evaluation of disease activity and response to therapy, using a panel of clinical, biological and imaging techniques. 1.3 Study design Dual centre, 24-week open-label randomised study in subjects with clinically active peripheral PsA receiving treatment with the relevant drugs. Synovial biopsies will be obtained from patients before and after 24 weeks of treatment with the different drugs. 1.4 Study population DMARD-resistant, biological naive patients with a diagnosis of psoriatic arthritis according to the CASPAR criteria with at least one swollen joint (either small or big joint) who are planning to receive treatment with one of the targeted drugs. In total, 36 patients will be included. Patients will be randomized 1:1:1 between: Group 1 (n=12): ustekinumab 45 mg (or 90 mg for patients > 100 kg) subcutaneously at baseline (W0), 4 weeks later (W4), and every 12 weeks until week 24 (i.e. W0, W4, and W16). Group 2 (n=12): guselkumab 100 mg subcutaneously (regardless of the weight of the patient) at weeks 0 and 4, followed by a maintenance dose every 8 weeks through week 24 (i.e. W0, W4, W12 and W20). Group 3 (n=12): adalimumab 40 mg (regardless of the weight of the patient), subcutaneously every other week, starting from the baseline until week 24 (i.e.W0, W2, W4, W6, W8, W10, W12, W14, W16, W18, W20 and W22). 1.5 Synovial biopsy procedure Synovial biopsies will be harvested either by ultrasound guided biopsy (USGB) for small joints (wrist, MCP, PIP), or large joints (elbow, knee, ankle) or by needle-arthroscopy procedure (NAP) for large joints such as the knee. In the case of large joint involvement, the same joint will be biopsied at W0 and W24. Based on our experience, repeating the procedure in a large joint, even if it is not swollen, is readily achieved by NAP. In the case of small joint involvement, the choice of the joint to biopsy will be based on ultrasound (US) examination. An US assessment with a score of more than 2 on Grey Scale/Power Doppler (see data on US scoring below in appendices) increases the amount of gradable synovial tissue after the procedure, and the quality of the RNA extracted from the synovial tissue. If the small joint biopsied at W0 is not clinically affected and/or has low US Grey Scale/Power Doppler scores lower by W24, another small joint will be considered for the biopsy if clinically affected. However, At W24 the procedure will be done preferably in the same joint, in order to avoid bias or too much heterogeneity in the analyses of the data. A window of no more than 15 days is allowed around the baseline (W0) and W24 visit. 1.6 Main study parameters/endpoints Primary endpoints:
- - identification of molecular pathways targeted by ustekinumab, guselkumab versus TNF-blockade in synovial biopsies (total and single cells) from PsA patients with active disease despite a csDMARDs, obtained prior to and 24 weeks after initiation of therapy.
- - clinical response at W24, by using DAS-44 or ACR20/50/70 response criteria.
- - identification of candidate synovial markers/pathways associated with response to ustekinumab, guselkumab, and anti-TNFalpha therapy in PsA by correlating molecular signals at baseline with the clinical response observed at week 24.
- - composite analyses of the association between molecular changes induced by anti-IL23, anti-IL23/12 and anti-TNF in the synovium, and core or non-core (clinical, biological, imaging) variables informative about response to therapy.
- - Chest x-ray A posterior-anterior view chest x-ray will be obtained locally at screening, unless results from a chest x-ray obtained no more than 3 months prior to the screening (or baseline) according to the general recommendations related to the use of biologics.
Group 1 (n=12): ustekinumab 45 mg (or 90 mg for patients > 100 kg) subcutaneously at baseline (W0), 4 weeks later (W4), and every 12 weeks until week 24 (i.e. W0, W4, and W16).
Group 2 (n=12): guselkumab 100 mg subcutaneously (regardless of the weight of the patient) at weeks 0 and 4, followed by a maintenance dose every 8 weeks through week 24 (i.e. W0, W4, W12 and W20).
Active Comparator: ADALIMUMAB
Group 3 (n=12): adalimumab 40 mg (regardless of the weight of the patient), subcutaneously every other week, starting from the baseline until week 24 (i.e.W0, W2, W4, W6, W8, W10, W12, W14, W16, W18, W20 and W22).
Procedure: - Global/single cell gene expression profiles obtained from Synovial biopsies
Global/single cell gene expression profiles obtained from synovial biopsies before and after 24 weeks of treatment with the drug.
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