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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05045001
Other study ID # IIBSP-IIL-2020-148
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 2, 2021
Est. completion date December 2022

Study information

Verified date April 2022
Source Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Contact Luis Sainz
Phone 679743541
Email lsainz@santpau.cat
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Tocilizumab and Sarilumab are first-line biological disease-modifying anti-rheumatic drug (bDMARD) which inhibits Interleukin 6 (IL-6) pathway through blockade of its receptor on the treatment of Rheumatoid Arthritis and other rheumatic diseases as Giant Cell Arteritis, Still's disease and Idiopathic Juvenile Arthritis. At present, there is a lack of evidence to recommend the treatment of one bDMARD over another. Seeking for genetic biomarkers to predict response to treatment could be key towards a personalized treatment strategy in rheumatology. The investigators aime to evaluate whether functional single nucleotide polymorphisms (SNPs) in the IL6R gene could predict response and/or toxicity in patients with rheumatic diseases treated with anti-IL-6 receptor drugs.


Recruitment information / eligibility

Status Recruiting
Enrollment 140
Est. completion date December 2022
Est. primary completion date June 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Diagnosis of Rheumatoid Arthritis by the American College of Rheumatology (ACR) 2010 criteria or - Diagnosis of Giant Cell Arteritis by the International League of Associations for Rheumatology (ILAR) criteria or - Diagnosis of Still disease by classification criteria (Yamaguchi et al.) or - Diagnosis of Idiopathic Juvenile Arthritis by ACR 1990 criteria. - All of the previous must have been treated with anti-IL-6R monoclonal antibodies in the last 5 years Exclusion Criteria: - <18 years at recruitment - Another rheumatic disease different of the ones in the inclusion criteria

Study Design


Locations

Country Name City State
Spain Hospital de la Santa Creu i Sant Pau Barcelona

Sponsors (1)

Lead Sponsor Collaborator
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary DAS28-C-reactive Protein (CRP) change Activity measure for patients with Rheumatoid Arthritis (RA) at 6 months
Primary Rate of adverse events Known adverse events during treatment with anti-IL6R drugs During treatment with anti-IL6R drugs
Primary CRP change Acute phase reactant reduction in the other diseases different of RA. 6 months
Primary Erythrocyte sedimentation rate (ESR) change Acute phase reactant reduction in the other diseases different of RA. 6 months
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