Randomized Trial Comparing Efficacy of Adalimumab, Anakinra and Tocilizumab in Non-infectious Refractory Uveitis

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:

• Active inflammatory chorioretinal and/or inflammatory retinal vascular lesions and/or macular edema (CRT ≥300 microns) OR
• Vitreous haze grade ≥4 on the Miami 9-step scale (or VH >1+ according to SUN/NEI classification)
• 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:

• oral
• intravaginal
• transdermal
• progestogen-only hormonal contraception associated with inhibition of ovulation 1:

• oral
• injectable
• implantable
• 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:

• Fever or infection requiring treatment with antibiotics within 3 weeks prior to Inclusion
• History of recurrent infection or predisposition to infection
• Known immunodeficiency
• History of multiple sclerosis and/or demyelinating disorder
• Laboratory values assessed during Inclusion:

• Hemoglobin < 8g/dL
• White Blood Cell Count (WBC) < 2.0 x 10^3/mm3
• Platelet count < 80 x 10^3/mm3
• Glomerular filtration rates (GFR) <30ml/min.
• Transaminases > 3 times upper normal value
• Use of the following systemic treatments during the specified periods:

• Any other previous systemic biologic therapy
• Treatment with any systemic alkylating agents within 12 months prior to Inclusion or between Inclusion and Day 0 (e.g., cyclophosphamide, chlorambucil)
• Any live (attenuated) vaccine within 3 months prior to Inclusion
• Use of the following ocular treatments during the specified periods:

• Previous anti Vascular Endothelial Growth Factor (VEGF) intravitreal therapy (applied to both eyes) within 3 months prior to Inclusion, or anticipated use during the study period
• Treatment with dexamethasone intravitreal implant [Ozurdex®]) within 6 months prior to Inclusion
• Intravitreal corticosteroids within 3 months prior to Inclusion. Previous Subtenon's corticosteroid injections are permitted if administered at least 2 months prior to Inclusion
• Stage III and IV New York Heart Association (NYHA) cardiac insufficiency