ClinConnect ClinConnect Logo
Search / Trial NCT03649061

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

Cobra Slim Accelerated Access To Anti Tnf Treat To Target Remission Induction

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.

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

0 patients applied

Trial Officials

Patrick Verschueren, MD, PhD

Principal Investigator

UZ Leuven

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Similar Trials