COBRA-Slim With or Without Fast Access to TNF Blockade for Remission Induction in Early RA
Launched by P. VERSCHUEREN · Aug 23, 2018
Trial Information
Current as of May 21, 2025
Completed
Keywords
ClinConnect Summary
No description provided
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Age 18 years and older
- • Diagnosis of RA as defined by the American College of Rheumatology (ACR)/ European League Against Rheumatism (EULAR) 2010 criteria for early RA
- • Early RA defined by a diagnosis made ≤ 1 year ago.
- • Use a reliable method of contraception for women of childbearing potential to be evaluated as in daily clinical practice
- • Able and willing to give written informed consent and to participate in the study
- • Understanding and able to write Dutch or French
- Exclusion Criteria:
- * Previous treatment with:
- • Methotrexate (MTX) or leflunomide
- • cyclophosphamide, azathioprine or cyclosporine
- • sulphasalazine (SSZ) for more than 3 weeks
- • hydroxychloroquine for more than 6 weeks
- • oral Glucocorticoids (GC) for more than 4 weeks within 4 months before screening
- • oral GC at a daily dosage of more than 10 mg prednisone equivalent within 4 weeks before baseline
- • oral GC at a daily dosage equal to or less than 10 mg prednisone equivalent within 2 weeks before baseline
- • intra-articular GC within 4 weeks before BL
- • an investigational drug for the treatment/prevention of RA
- • History of chronic heart failure
- • History of severe infections or chronic infection
- • History of malignant neoplasm within 5 years
- • Contra indications for GC
- • Contra indications for TNF blocking agents
- • Contra indications for MTX or leflunomide
- • Psoriatic Arthritis
- • Underlying cardiac, pulmonary, metabolic, renal or gastrointestinal conditions, chronic or latent infectious diseases or immune deficiency which in the opinion of the investigator places the patient at an unacceptable risk for participation in the study
- • Pregnancy, breastfeeding or no use of a reliable method of contraception for woman of childbearing potential (as in daily clinical practice)
- • Alcohol or drug abuse
- • Active tuberculosis (TB)
- • Latent TB unless adequate prophylactic treatment is given according to local guidelines
- • No access to the Belgian Health Insurance system-
About P. Verschueren
P. Verschueren is a dedicated clinical trial sponsor committed to advancing medical research and improving patient outcomes through innovative study designs and rigorous methodologies. With a focus on collaboration and ethical practices, the organization supports a diverse range of clinical trials across various therapeutic areas. P. Verschueren leverages a team of experienced professionals and state-of-the-art technologies to ensure the highest standards of data integrity and regulatory compliance. Their mission is to contribute to the development of safe and effective therapies by fostering partnerships with healthcare providers, research institutions, and regulatory agencies.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Leuven, , Belgium
Brussels, , Belgium
Liège, , Belgium
Hasselt, Limburg, Belgium
Bonheiden, Antwerpen, Belgium
Herentals, Antwerpen, Belgium
Merksem, Antwerpen, Belgium
Gilly, Henegouwen, Belgium
Genk, Limburg, Belgium
Genk, Limburg, Belgium
Yvoir, Namur, Belgium
Aalst, Oost Vlaanderen, Belgium
Leuven, Vlaams Brabant, Belgium
Vilvoorde, Vlaams Brabant, Belgium
Brugge, West Vlaanderen, Belgium
Brugge, West Vlaanderen, Belgium
Brussel, , Belgium
Brussel, , Belgium
Brussel, , Belgium
Patients applied
Trial Officials
Patrick Verschueren, MD, PhD
Principal Investigator
UZ Leuven
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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