E.1 Medical condition or disease under investigation |
E.1.1 | Medical condition(s) being investigated |
Subjects with clinically quiescent sight threatening, non-infectious, intermediate-, anterior and intermediate-, posterior- or pan-uveitis.
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MedDRA Classification |
E.1.2 Medical condition or disease under investigation |
E.1.2 | Version | 8.1 |
E.1.2 | Level | LLT |
E.1.2 | Classification code | 10046851 |
E.1.2 | Term | Uveitis |
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E.1.3 | Condition being studied is a rare disease | No |
E.2 Objective of the trial |
E.2.1 | Main objective of the trial |
The objective of this study is to assess the safety and efficacy of LX211 as therapy in subjects with clinically quiescent sight-threatening, non-infectious intermediate-, anterior and intermediate-, posterior- or pan- uveitis. |
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E.2.2 | Secondary objectives of the trial |
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E.2.3 | Trial contains a sub-study | No |
E.3 | Principal inclusion criteria |
• A diagnosis of non-infectious intermediate-, anterior and intermediateposterior- or pan- uveitis of at least three months duration prior to enrollment, requiring treatment during that period to control intraocular inflammatory disease and avoid sight-threatening complications due to inflammation. Subjects are anticipated to have, but are not restricted to, the following conditions: intermediate uveitis of the pars planitis subtype, sarcoidosis, the Vogt-Koyanagi-Harada (VKH) syndrome, birdshot retinochoroidopathy, retinal vasculitis, sympathetic ophthalmia and multifocal choroiditis with panuveitis • Minimum prescribed therapy upon enrollment is either a dose averaging ≥ 10 mg/day of systemic prednisone or equivalent or a more intensive immunosuppression regimen (e.g. corticosteroid combined with a corticosteroid-sparing agent) and/or repeated periocular/intravitreal corticosteroid administration (i.e. ≥ 2 administrations within the previous 6 months) for control of inflammatory disease. More intensive regimens may include one additional immunosuppressive drug from among the following (or related) compounds: - cyclosporine - tacrolimus - azathioprine - mycophenolate mofetil - methotrexate • Subjects who are intolerant of local corticosteroid therapy due to the development of an ocular hypertensive episode • Subjects may also enter the study if they are receiving treatment with topical corticosteroids for control of anterior inflammation • Subjects may also enter the study if they are receiving treatment with a single immunomodulatory drug for uveitis control • The subject’s uveitis is considered clinically quiescent on current medications at the time of enrollment. Clinical quiescence means that the prescribed dosage(s) for their current uveitis medications at enrollment have neither been increased in the 6 weeks prior to enrollment, nor there have been any symptoms, signs or history of exacerbation of intraocular inflammation during this same 6-week period • Subjects are considered by the investigator to require corticosteroid-sparing therapy. Reasons may include such considerations as need for steroidsparing therapy, corticosteroid-intolerance, history of diabetes, adverse experiences with current therapy or conditions for which immunosuppressive therapy is used typically (e.g. posterior uveitides, birdshot retinochoroidopathy, multifocal choroiditis with panuveitis) • Subjects have BCVA in the worst involved eye of 20/400 or better (ETDRS logMAR < 1.34) • Subjects do not plan to undergo elective ocular surgery (e.g., cataract extraction) during the course of the study • At least 13 years of age • Subjects, whether male or female, with reproductive potential and who are sexually active agree to use double-barrier contraception methods throughout the course of the study (minimum of 26 weeks) • Women of childbearing potential must have a negative urine pregnancy test (UPT) within 48 hours prior to starting study drug and must not be lactating Female subjects of non-childbearing potential must meet at least one of the following criteria: 1. Postmenopausal females, defined as: a. Females over the age of 60 years. b. Females who are 45 to 60 years of age must be amenorrheic for at least 2 years. 2. Females who had a hysterectomy and/or bilateral oophorectomy. All other female subjects (including females with tubal ligations) will be considered to be of childbearing potential. • Subjects weigh at least 38 kg (84 lbs) and no more than 110 kg (242 lbs). (Note: this restriction is imposed to allow for the masking of treatment assignments.) • Subjects or their guardians must be capable of understanding the purpose and risks of the study; able to give informed consent (and assent by pediatric subjects, if required) and to comply with the study requirements |
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E.4 | Principal exclusion criteria |
• Uveitis of infectious etiology • Clinically suspected or confirmed central nervous system or ocular lymphoma • A primary diagnosis of anterior uveitis • Evidence of active, uncontrolled non-infectious uveitis • Uncontrolled glaucoma • A history or diagnosis of Behçet’s disease (since tapering or withdrawal of concomitant immunosuppressive medications is not a usual standard-of-care for Behçet’s subjects) • Local (periocular/intravitreal) administration of corticosteroids within the previous 6 weeks • Any implantable corticosteroid-eluting device (eg, Retisert™, Posurdex®, Medidur™, I-vation™ TA intravitreal implant) • An immune suppression regimen that includes an alkylating agent within the previous 90 days • Subjects who have received treatment with a monoclonal antibody or any other biologic therapy within the previous 90 days or with alemtuzumab within the previous 12 months • Subjects who have used any drugs or substances known to be strong inhibitors of CYP 3A4/5 enzymes within 7 days of the first dose, or grapefruit juice and star fruit within 24 hours of the first dose (listed in table of CYP 3A4/5, Section 9.7) • Subjects who have taken any other medications listed in Section 9.7, within the timeframe specified, prior to the first dose • Recipients of a solid organ transplant • Subjects with chronic hypotony (less than 6 mmHg) • Subjects with lens opacities or obscured ocular media upon enrollment such that reliable evaluation and grading of the posterior segment cannot be performed • Presence of an ocular toxoplasmosis scar • A known history or clinical diagnosis of herpes zoster or varicella infection within 6 weeks prior to enrollment, or chicken pox exposure within 21 days before enrollment • Subjects with diabetes mellitus that is inadequately controlled • Active, extraocular infection requiring the prolonged or chronic use of antimicrobial agents or the presence of active hepatitis A, B or C virus (HAV, HBV, HCB) • Subjects who have a history of or exposure to syphilis, Lyme , or toxoplasmosis • Modification of Diet in Renal Disease Study (MDRD) glomerular filtration rate (GFR) < 60 mL/min • Alanine transaminase (ALT), aspartate transaminase (AST), or gammaglutamyl transferase (GGT) ≥ 3x upper limit of normal (ULN) • Severe anemia (hemoglobin < 6 g/dL), leukopenia (white blood cell count[WBC] < 2500 mm3), thrombocytopenia (platelet count < 80,000 mm3), polycythemia (hematocrit [Hct] > 54% [male] or Hct > 49% [female]) or clinically significant coagulopathy • Seropositivity for human immunodeficiency virus (HIV) • Current malignancy or a history of malignancy (within the previous 5 years) except non-metastatic basal or squamous cell carcinoma of the skin or carcinoma-in-situ of the cervix that has been treated successfully • Previous exposure or known contraindication to administration of LX211 (ISA247) or any of its components • History of clinically defined allergy to any of the constituents of the LX211 formulation (vitamin E, medium chain triglyceride [MCT] oil, Tween 40, ethanol) • Using a therapy for a condition other than uveitis that would likely affect immune responses or interfere with trial logistics • Currently enrolled in another clinical therapeutic trial or who have received any investigational therapy within the 30 days prior to enrollment and/or has not recovered from any reversible effects or side effects of prior investigational agent • Subject with any non-ocular, medically significant co-morbid conditions that impair normal activities, require immunosuppression, or that would likely have an impact on the subject’s ability to comply with the study visit schedule • Any current or history of substance abuse, psychiatric disorder or a condition that, in the opinion of the investigator, may invalidate communication • A significant local or systemic infection requiring medical treatment at the time of enrollment |
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E.5 End points |
E.5.1 | Primary end point(s) |
The primary endpoint is the proportion of subjects who experience inflammatory exacerbation during the 26 weeks of treatment as defined by a clinically significant deterioration in either eye in one or more of the following:
• vitreous haze: an increase of ≥2 grades from baseline. • anterior chamber cells: an increase of ≥2 grades from baseline. • visual acuity: a change of ≥+0.3 logMAR from baseline in BCVA. |
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E.6 and E.7 Scope of the trial |
E.6 | Scope of the trial |
E.6.1 | Diagnosis | No |
E.6.2 | Prophylaxis | No |
E.6.3 | Therapy | Yes |
E.6.4 | Safety | Yes |
E.6.5 | Efficacy | Yes |
E.6.6 | Pharmacokinetic | No |
E.6.7 | Pharmacodynamic | No |
E.6.8 | Bioequivalence | No |
E.6.9 | Dose response | No |
E.6.10 | Pharmacogenetic | No |
E.6.11 | Pharmacogenomic | No |
E.6.12 | Pharmacoeconomic | No |
E.6.13 | Others | No |
E.7 | Trial type and phase |
E.7.1 | Human pharmacology (Phase I) | No |
E.7.1.1 | First administration to humans | No |
E.7.1.2 | Bioequivalence study | No |
E.7.1.3 | Other | Yes |
E.7.1.3.1 | Other trial type description | |
E.7.2 | Therapeutic exploratory (Phase II) | Yes |
E.7.3 | Therapeutic confirmatory (Phase III) | Yes |
E.7.4 | Therapeutic use (Phase IV) | No |
E.8 Design of the trial |
E.8.1 | Controlled | Yes |
E.8.1.1 | Randomised | Yes |
E.8.1.2 | Open | No |
E.8.1.3 | Single blind | No |
E.8.1.4 | Double blind | Yes |
E.8.1.5 | Parallel group | Yes |
E.8.1.6 | Cross over | No |
E.8.1.7 | Other | No |
E.8.2 | Comparator of controlled trial |
E.8.2.1 | Other medicinal product(s) | No |
E.8.2.2 | Placebo | Yes |
E.8.2.3 | Other | No |
E.8.3 |
The trial involves single site in the Member State concerned
| No |
E.8.4 | The trial involves multiple sites in the Member State concerned | Yes |
E.8.4.1 | Number of sites anticipated in Member State concerned | 5 |
E.8.5 | The trial involves multiple Member States | Yes |
E.8.5.1 | Number of sites anticipated in the EEA | 18 |
E.8.6 Trial involving sites outside the EEA |
E.8.6.1 | Trial being conducted both within and outside the EEA | Yes |
E.8.6.2 | Trial being conducted completely outside of the EEA | Information not present in EudraCT |
E.8.6.3 | If E.8.6.1 or E.8.6.2 are Yes, specify the regions in which trial sites are planned |
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E.8.7 | Trial has a data monitoring committee | Yes |
E.8.8 |
Definition of the end of the trial and justification where it is not the last
visit of the last subject undergoing the trial
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Last visit of last subject. |
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E.8.9 Initial estimate of the duration of the trial |
E.8.9.1 | In the Member State concerned years | 1 |
E.8.9.1 | In the Member State concerned months | 6 |
E.8.9.1 | In the Member State concerned days | |
E.8.9.2 | In all countries concerned by the trial years | 1 |
E.8.9.2 | In all countries concerned by the trial months | 6 |