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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02963402
Other study ID # IIBSP-TOC-2016-09
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 9, 2016
Est. completion date October 1, 2018

Study information

Verified date November 2018
Source Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

We can speculate that the best responders to tocilizumab should have multiple related elements (Treg CD39, adenosine, IL-35) successfully induced and expressed in order to play its beneficial role. The study of these elements and its pathways could help identify the best responders to tocilizumab treatment.


Recruitment information / eligibility

Status Completed
Enrollment 35
Est. completion date October 1, 2018
Est. primary completion date October 1, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Patients of all sexes, aged = 18 years.

- RA Patients (according to ACR / EULAR criteria 2010) of moderate to severe activity (DAS 28> 3.2 or SDAI> 11), and 6 months or more of evolution, starting treatment with ACTEMRA (tocilizumab) or with an anti-TNF, according to the product data.

- Patients with body weight = 150 kg.

- Patients who have received written information about the study and gave their informed consent to participate in the study

Exclusion Criteria:

- Patients with a history of autoimmune disease or inflammatory joint disease other than RA.

- Patients treated with any investigational agent within 4 weeks (or 5 half-lives of investigational agent, whichever is greater) before starting treatment with tocilizumab

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Tocilizumab

Adalimumab


Locations

Country Name City State
Spain Insitut de Recerca 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 Treg phenotype Baseline to 6 months change
Primary ATP (adenosine triphosphate) Baseline to 6 months change
See also
  Status Clinical Trial Phase
Completed NCT01288287 - Long Term Effects of an Early Response to Certolizumab Pegol (CZP, Cimzia®) in Rheumatoid Arthritis (RA) Patients N/A