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An Open-Label Extension of the Dose Finding Study (DSC/08/2357/36) in Patients With Poly Juvenile Idiopathic Arthritis (JIA)

This study has been terminated.
(Previous study DSC/08/2357/36 did not show efficacy for Givinostat in JIA. Decision wasn't related to any tolerability concerns)
Information provided by (Responsible Party):
Italfarmaco Identifier:
First received: March 14, 2012
Last updated: February 26, 2014
Last verified: February 2014
Givinostat is expected to exert a clinically relevant therapeutic effect on polyarticular JIA through the inhibition of the production/release of pro-inflammatory cytokines, such as IL-1β, IL-6 and TNFα, which are involved in the pathogenesis of the arthritic process.

Condition Intervention
Juvenile Idiopathic Arthritis Drug: Givinostat

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: An Open-Label Extension of the Dose Finding Study (DSC/08/2357/36) in Patients With Polyarticular Course Juvenile Idiopathic Arthritis (Poly JIA) JIA

Resource links provided by NLM:

Further study details as provided by Italfarmaco:

Primary Outcome Measures:
  • long-term safety [ Time Frame: 1 year ]
    Incidence of SAEs and AEs of interest

Secondary Outcome Measures:
  • ACR pediatric 30 level of response [ Time Frame: 3 months ]
    To maintan the Pediatric ACR 30 level(ACR: American COllege of Rheumatology) reached during the participation to the previous study (DSC/08/2357/36)

  • ACR pediatric 50 and 70 levels of response [ Time Frame: 3 months ]
    To improve the Pediatric ACR levels to PedACR50 or PedACR70

Enrollment: 1
Study Start Date: December 2011
Study Completion Date: January 2014
Primary Completion Date: January 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Givinostat Drug: Givinostat
oral suspension, 0,75 mg/Kg b.i.d. in fed conditions


Ages Eligible for Study:   2 Years to 18 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • subjects who had successfully completed the previous Dose Finding Study and were fully compliant to the inclusion/exclusion criteria described in the previous DSC/08/2357/36

Exclusion Criteria:

  • patients with fever related to JIA or other systemic features of JIA during 12 months before entering the study
  • active bacterial or mycotic infection requiring antimicrobial treatment
  • episode of macrophage activation syndrome over the last 6 months
  • baseline prolongation of QT/QTc interval, use of concomitant medications that prolong the QT/QTc interval or history of additional risk factors for TdP.
  • clinically significant cardiovascular disease
  • clinically significant illness i.e. any condition that in the opinion of the Investigator places the patient to unacceptable risk for adverse outcome if he/she were to participate in the study
  • psychiatric illness/social situation that would limit compliance with study medication and protocol requirements
  • inherited metabolic diseases
  • presence of malignancy
  • pregnancy or lactation
  • positive blood test for HIV
  • active EBV infection, active B and/or C hepatitis
  • platelet count <100x10(9)/L
  Contacts and Locations
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Please refer to this study by its identifier: NCT01557452

Czech Republic
1st Faculty of Medicine and General Faculty Hospital
Praha, Czech Republic, 12109
Sponsors and Collaborators
  More Information

Responsible Party: Italfarmaco Identifier: NCT01557452     History of Changes
Other Study ID Numbers: DSC/11/2357/42
Study First Received: March 14, 2012
Last Updated: February 26, 2014

Keywords provided by Italfarmaco:

Additional relevant MeSH terms:
Arthritis, Juvenile
Joint Diseases
Musculoskeletal Diseases
Rheumatic Diseases
Connective Tissue Diseases
Autoimmune Diseases
Immune System Diseases processed this record on September 21, 2017