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About
RUBI, is the first prospective randomized, head to head study, comparing Adalimumab to either anakinra, or tocilizumab in refractory Non Infectious Uveitis (NIU). There is no firm evidence or randomized controlled trials directly addressing the best biologic agent in severe and refractory NIU. NIU can cause devastating visual loss and up to 20% of legal blindness. Corticosteroids and immunosuppressants failed to demonstrate sustainable remission over 70 % of refractory/relapsing severe uveitis. The incidence of blindness in NIU has been dramatically reduced in the recent years with the use of biologics, raising the question of whether these compounds should be used earlier in the treatment of severe non infectious uveitis. Contrasting with immunosuppressors, biotherapies act rapidly and are highly effective in steroid's sparing thus preventing occurrence of cataract and/or glaucoma.
Despite a strong rationale, these compounds are not yet approved in uveitis, which guarantees the innovative nature of this study that aims selecting or dropping any arm when evidence of efficacy already exists.
Enrollment
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Ages
Volunteers
Inclusion criteria
Provide written, informed consent prior to the performance of any study specific procedures
Diagnosis of non-infectious intermediate, posterior-, or pan-uveitis in at least one eye fulfilling the International Study Group Classification Criteria (Standardization of Uveitis Nomenclature [SUN] criteria) of posterior, or pan- uveitis confirmed by documented medical history
Currently uncontrolled uveitic disease. Uncontrolled uveitic disease is defined as fulfilling one of the two following criteria at Inclusion:
a. Patient who are receiving prednisone ≥10 mg/day and <80mg/day (or equivalent dose of another corticosteroid) at stable dose 30 days prior to the first study drug administration on Day 0 and who received at least 1 other systemic immunosuppressant (All systemic immunosuppressants must have been discontinued 30 days prior to the first study drug administration on Day 0), or, b. Patient who received IFN alpha (All systemic immunosuppressants must have been discontinued 30 days prior to the first study drug administration on Day 0), or, c. To be intolerant to immunosuppressant
Best corrected visual acuity (BCVA) by ETDRS ≥ to 20/400 in either eye
Stable dose for two weeks prior to inclusion of topical corticosteroids and/or NSAIDs
Male or female , Age >= 18 years at Inclusion
Weight 40 - 120 kg (88.2 - 264 lbs) at Inclusion
Chest X-ray or thoracic CT scan results (postero-anterior and lateral) within 12 weeks prior to Inclusion with no evidence of active Tuberculosis, active infection, or malignancy
For female subjects of child-bearing age, a negative serum or urine pregnancy test
For subjects with reproductive potential, a willingness to use contraceptive measures adequate to prevent the subject or the subject's partner from becoming pregnant during the study and 3 and 5 months after stopping therapy for roactemra and adalimumab, respectively. Birth control methods which may be considered as highly effective methods that can achieve a failure rate of less than 1% per year when used consistently and correctly are considered as highly effective birth control methods (according to CTFG recommendations). Such methods include :
combined (estrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation 1:
progestogen-only hormonal contraception associated with inhibition of ovulation 1:
intrauterine device (IUD)
intrauterine hormone-releasing system ( IUS)
bilateral tubal occlusion
vasectomised partner
sexual abstinence (In the context of this guidance sexual abstinence is considered a highly effective method only if defined as refraining from heterosexual intercourse during the entire period of risk associated with the study treatments. The reliability of sexual abstinence needs to be evaluated in relation to the duration of the clinical trial and the preferred and usual lifestyle of the subject).
A QuantiFERON®-Tuberculosis (TB) test within 6 months prior to Screening
Exclusion criteria
Infectious uveitis, masquerade syndromes (idiopathic uveitis is permitted)
Isolated anterior uveitis
Presence of cataract or posterior capsular opacification so severe that an assessment of the posterior segment of either eye is inadequate or impossible
Contraindication to mydriasis in either eye or presence of posterior synechiae in the study eye such that mydriasis is inadequate for posterior segment examination
Intraocular pressure ≥ 25 mmHg by Goldmann tonometry or advanced glaucoma in either eye
Monocular patient
Active tuberculosis
Known positive syphilis serology, HIV antibody, hepatitis B surface antigen and/or anti-nucleocapsid antibody of hepatitis B virus and/or Hepatitis C virus, within 1 month prior to inclusion.
History of malignancy within 5 years prior to Inclusion other than carcinoma in situ of the cervix or adequately treated, non-metastatic squamous or basal cell carcinoma of the skin.
History of severe allergic or anaphylactic reactions to monoclonal antibodies
Infectious disease:
Known immunodeficiency
History of multiple sclerosis and/or demyelinating disorder
Laboratory values assessed during Inclusion:
Use of the following systemic treatments during the specified periods:
Use of the following ocular treatments during the specified periods:
Stage III and IV New York Heart Association (NYHA) cardiac insufficiency
Primary purpose
Allocation
Interventional model
Masking
112 participants in 3 patient groups
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Central trial contact
matthieu Resche-Rigon, MD PHD; David Saadoun, MD PHD
Data sourced from clinicaltrials.gov
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