CLINICAL TRIAL UPDATE

DRY AMD

Study: Study to Assess the Safety and Effects of Cells Injected Intravitreal in Dry Macular Degeneration

Sponsor: Bioheart, Inc.

Purpose: To evaluate the treatment of dry AMD with adipose stem cell implantation

Design: Interventional, Single Group, Open Label

Number of Patients: 100

Inclusion Criteria: Dry AMD; VA in the study <20/200

Exclusion Criteria: Females who are pregnant or nursing or females of childbearing potential who are unwilling to maintain contraceptive therapy for the duration of the study; inability to undergo syringe liposuction procedure

Information: kcomella@bioheartinc.com

Study: NEAMD: Non-exudative Age-related Macular Degeneration

Sponsor: Oregon Health and Science University

Purpose: To use OCT technology to compare how the retinal anatomy and blood flow differ within three severity groupings of non-exudative AMD

Design: Observational, Case Control, Prospective

Number of Patients: 20

Inclusion Criteria: Presence of mild, moderate or severe NEAMD; media clarity, pupillary dilation, and subject cooperation sufficient for adequate fundus photographs; vision better than 20/200

Exclusion Criteria: Inability to maintain stable fixation for OCT imaging. A condition that, in the opinion of the investigator, would preclude participation in the study; a concurrent ocular pathology that may contribute to vision loss

Information: (503) 494-3000

Study: I-TEAM: Intervention Trial in Early Age-related Macular Degeneration

Sponsor: Newtricious R&D BV

Purpose: To assess whether there is a change in visual function and status of the retina after a year of intervention in subjects with early signs of AMD

Design: Randomized, Efficacy, Parallel Assignment, Double-blind

Number of Patients: 120

Inclusion Criteria: Many small drusen, or a few intermediate-sized (63-124 µm) drusen, or macular pigmentary changes

Exclusion Criteria: Ocular media opacity (severe cataract); history of active small bowel disease or resection; atrophic gastritis; hyperlipidemia (LDL >120 mg/dL or triglycerides >400 mg/dL)

Information: ian.j.murray@manchester.ac.uk

Study: Study on Visual Function Impairments in Dry Age-related Macular Degeneration

Sponsor: Duke University

Purpose: To submit enrollees to the visual function testing

Design: Observational, Prospective

Number of Patients: 190

Inclusion Criteria: Has been diagnosed with dry AMD stages 1-3

Exclusion Criteria: Presence of retinal pathology such as central geographic atrophy, hemorrhage or retinal fluid, and other macular pathology other than AMD

Information: (919) 684-9010

Study: Pharmacokinetic and Pharmacodynamic Study of Emixustat in Subjects With Geographic Atrophy Associated With Dry AMD

Sponsor: Acucela, Inc.

Purpose: To characterize emixustat hydrochloride pharmacokinetic and pharmacodynamic parameters in subjects with GA associated with dry AMD

Design: Randomized, Pharmacokinetics/Dynamics, Crossover, Double-blind

Number of Patients: 26

Inclusion Criteria: Clinical diagnosis of GA associated with AMD

Exclusion Criteria: GA associated with a condition other than AMD; history of active or high risk of developing CNV in either eye; known serious allergy to the fluorescein sodium for injection in angiography

Information: clinicaltrials@acucela.com

Study: Phase II/III Study of the Efficacy and Safety of MacuCLEAR MC-1101 in Treating Dry Age-Related Macular Degeneration

Sponsor: MacuCLEAR, Inc.

Purpose: To assess the efficacy, safety, and tolerability of MC-1101 for these patients

Design: Randomized, Safety/Efficacy, Parallel Assignment, Double-blind

Number of Patients: 60

Inclusion Criteria: 20/80 or better ETDRS best-corrected visual acuity; early to intermediate nonexudative AMD (AMD category 3 through 3b on Age-Related Eye Disease Study [AREDS] Report No. 8 AMD Categories

Exclusion Criteria: Past or current exudative AMD or central geographic atrophy in study eye; (AMD Category 4 on Age-Related Eye Disease Study (AREDS) Report No. 8 AMD Categories); past or current retinal or choroidal vasculopathy in study eye (eg, serous or hemorrhagic pigment epithelial detachment, polypoidal choroidal vasculopathy, central serous chorioretinopathy, retinal vein occlusion, sickle cell retinopathy)

Information: pralston@macuclear.com

Study: SPECTRI: A Study Investigating the Safety and Efficacy of Lampalizumab Intravitreal Injections in Patients With Geographic Atrophy Secondary to Age-Related Macular Degeneration

Sponsor: Hoffmann-La Roche

Purpose: To conduct a study evaluating the efficacy and safety of lampalizumab administered by intravitreal injections in patients with geographic atrophy (GA) secondary to age-related macular degeneration

Design: Randomized, Safety/Efficacy, Parallel Assignment, Double-blind

Number of Patients: 936

Inclusion Criteria: Well demarcated area(s) of GA secondary to AMD with no evidence of prior or active choroidal neovascularization (CNV) in both eyes

Exclusion Criteria: History of vitrectomy surgery, submacular surgery, or other surgical intervention for AMD; previous laser photocoagulation for CNV, diabetic macular edema, retinal vein occlusion, and proliferative diabetic retinopathy; previous intravitreal drug delivery (eg, intravitreal corticosteroid injection, anti-angiogenic drugs, anti-complement agents, or device implantation)

Information: global.rochegenentechtrials@roche.com

DRY AMD

Study: BEACON: A Safety and Efficacy Study of Brimonidine Intravitreal Implant in Geographic Atrophy Secondary to Age-related Macular Degeneration

Sponsor: Allergan

Purpose: To assess the safety and efficacy of the brimonidine intravitreal implant in patients with geographic atrophy due to age-related macular degeneration

Design: Randomized, Safety/Efficacy, Parallel Assignment, Double-blind

Number of Patients: 300

Inclusion Criteria: Geographic atrophy due to age-related macular degeneration in the study eye; visual acuity better than or equal to 20/62 in the study eye and 20/200 in the fellow eye

Exclusion Criteria: Cataract surgery or laser-assisted in situ keratomileusis (LASIK) in the study eye in the last 3 months; infections in either eye in the last 3 months

Information: clinicaltrials@allergan.com

Study: CHROMA: A Study Investigating the Efficacy and Safety of Lampalizumab Intravitreal Injections in Patients With Geographic Atrophy Secondary to Age-Related Macular Degeneration

Sponsor: Hoffmann-La Roche

Purpose: To evaluate the efficacy and safety of lampalizumab administered by intravitreal injections in patients with geographic atrophy (GA) secondary to age-related macular degeneration

Design: Randomized, Safety/Efficacy, Parallel Assignment, Double-blind

Number of Patients: 936

Inclusion Criteria: Participants aged >/= 50 years; well demarcated area(s) of GA secondary to AMD with no evidence of prior or active choroidal neovascularization (CNV) in both eyes

Exclusion Criteria: History of vitrectomy surgery, submacular surgery, or other surgical intervention for AMD; previous laser photocoagulation for CNV, diabetic macular edema, retinal vein occlusion, and proliferative diabetic retinopathy; previous intravitreal drug delivery (eg, intravitreal corticosteroid injection, anti-angiogenic drugs, anti-complement agents, or device implantation); Ocular Exclusion Criteria: Both Eyes: GA in either eye due to causes other than AMD; previous treatment with eculizumab, lampalizumab and/or fenretinide

Information: global.rochegenentechtrials@roche.com

Study: TOGA: Clinical Study to Evaluate Treatment With ORACEA for Geographic Atrophy

Sponsor: Paul Yates, MD, PhD/MEDARVA

Purpose: To evaluate the efficacy and safety of ORACEA in the treatment of geographic atrophy due to dry age-related macular degeneration

Design: Randomized, Parallel Assignment, Double-blind

Number of Patients: 286

Inclusion Criteria: Best-corrected visual acuity of 20/20 - 20/400 in the study eye; best-corrected visual acuity of hand motion or better in the non-study eye; clinical diagnosis of geographic atrophy secondary to non-exudative age-related macular degeneration in at least one eye (study eye); geographic atrophy lesions of ≥ 0.5 and ≤ 7.0 MPS disc areas

Exclusion Criteria: History of or active presence of choroidal neovascularization secondary to exudative age-related macular degeneration in the study eye; history of or active presence of choroidal neovascularization secondary to exudative age-related macular degeneration in the non-study eye requiring any treatment within 12 months prior to Day 0 or expected to require treatment for the duration of the study; prior treatment for non-exudative age-related macular degeneration

Information: klh7v@virginia.edu

Study: A Study of Lampalizumab Intravitreal Injections Administered Every Two Weeks or Every Four Weeks to Patients With Geographic Atrophy

Sponsor: Genentech

Purpose: To investigate the exposure-response and safety of lampalizumab administered intravitreally every 2 weeks (Q2W) or every 4 weeks (Q4W) for 24 weeks in patients with geographic atrophy (GA) secondary to age-related macular degeneration

Design: Randomized, Safety/Efficacy, Parallel Assignment, Single-blind

Number of Patients: 100

Inclusion Criteria: Patients aged 60-89 years with well-demarcated area of GA secondary to AMD in the absence of choroidal neovascularization

Exclusion Criteria: History of vitrectomy surgery, submacular surgery, or other surgical intervention for AMD; previous subfoveal focal laser photocoagulation; laser photocoagulation in the study eye; previous intravitreal drug administration; GA in either eye due to causes other than AMD

Information: global.rochegenentechtrials@roche.com

Study: Study of Dark Adaptation in Age-related Macular Degeneration

Sponsor: National Eye Institute

Purpose: To evaluate the effectiveness of using a dark adaptation protocol to identify and monitor early to middle dry AMD

Design: Observational, Prospective

Number of Patients: 200

Inclusion Criteria: Group 0: No large drusen or advanced AMD; Group 1: At least one large drusen in the study eye and no large drusen or advanced AMD in the fellow eye; Group 2: Bilateral large drusen with or without RPE hypo/hyperpigmentary changes; Group 3: At least one large drusen in the study eye and advanced AMD in the fellow eye

Exclusion Criteria: Advanced AMD

Information: prpl@mail.cc.nih.gov

Study: RADIANT: Study of HUCNS-SC Subretinal Transplantation in Subjects With GA of AMD

Sponsor: StemCells, Inc.

Purpose: To evaluate the safety and efficacy of sub-retinal transplantation of stem cells in subjects with bilateral GA AMD

Design: Safety/Efficacy, Single Group, Single-blind

Number of Patients: 63

Inclusion Criteria: GA associated with AMD in both eyes. Total area of GA determined by fundus autofluorescence; BCVA of 20/320 or better in each eye at screening assessment

Exclusion Criteria: Prior or concurrent choroidal neovascularization in either eye by clinical exam and/or fluorescein angiography as determined by the investigator or the reading center; retinal or macular disease of any other cause in either eye; diagnosis of glaucoma in either eye; uncontrolled intraocular pressure in either eye

Information: kglocke@retinafoundation.org

WET AMD

Study: CFH&AMD: Complement Factor H Haplotypes and Smoking in Age-related Macular Degeneration

Sponsor: Department of Veterans Affairs

Purpose: To test the hypothesis that smoking increases AMD by increasing complement activation and that this is positively correlated with known disease variations in the CFH gene

Design: Observational, Cohort, Prospective

Number of Patients: 300

Exclusion Criteria: Ocular diseases that might simulate AMD or preclude its diagnosis

Information: rohrer@musc.edu

Study: Liberty: Impact of Home Monitoring to Decrease the Treatment Burden for Neovascular Age-related Macular Degeneration

Sponsor: Retinal Consultants of Arizona/Genentech

Purpose: To reduce the burden of in-office visits and injections

Design: Interventional, Randomized, Safety/Efficacy, Parallel Assignment, Open Label

Number of Patients: 60

Inclusion Criteria: Choroidal neovascular membrane (CNV) secondary to AMD, as confirmed by the patient’s medical history and a documented diagnosis of CNV; the study eye must have received at least 3 anti-Vascular endothelial growth factor (VEGF) treatments prior to the screening visit, with at least 2 anti-VEGF treatments over the preceding 3 months; best-corrected VA (BCVA) of 20/32 to 20/200 Snellen equivalent in the study eye

Exclusion Criteria: Choroidal neovascularization in the study eye due to any reason other than AMD; active uncontrolled glaucoma; had any intraocular surgeries in the study eye within 3 months of enrollment or are known or likely candidates for intraocular surgery (including cataract surgery) in the study eye within 1 year of enrollment

Information: RMcKusick@retinalconsultantsaz.com

Study: Phase 1 Study of Topical Ocular PAN-90806 for Neovascular Age-related Macular Degeneration

Sponsor: PanOptica, Inc.

Purpose: To assess the safety and tolerability of topical ocular PAN-90806 in patients with active, subfoveal choroidal neovascularization associated with neovascular AMD

Design: Interventional, Randomized, Safety, Parallel Assignment, Open Label

Number of Patients: 30

Inclusion Criteria: Diagnosis in the study eye of active, pathologic, newly diagnosed and previously untreated, subfoveal choroidal neovascular (CNV) lesions secondary to neovascular AMD

Exclusion Criteria: History of or current clinical evidence in the study eye of: aphakia, DME, any ocular inflammation or infections, pathological myopia, retinal detachment, advanced glaucoma, and significant media opacity, including cataract

Information: kcurtiss@panopticapharma.com

Study: RESCUE: Ranibizumab for Recalcitrant Wet Age-related Macular Degeneration in Eyes Previously Switched From Bevacizumab and/or Ranibizumab to Aflibercept

Sponsor: Northern California Retina Vitreous Associates/Genentech

Purpose: To determine the effectiveness of ranibizumab 0.5 mg or 1.0 mg in subjects who were previously treated with bevacizumab and subsequently switched to aflibercept

Design: Interventional, Nonrandomized, Efficacy, Parallel Assignment, Open Label

Number of Patients: 8

Inclusion Criteria: Best-corrected ETDRS VA between 20/25 to 20/320; total area of subretinal hemorrhage and/or fibrosis comprising less than 50% of lesion

Exclusion Criteria: History of prior vitrectomy surgery; previous treatment with photodynamic therapy, radiation, or any other intravitreal drug delivery

Information: alcon.medinfo@alcon.com

Study: Prospective Randomized Trial of Proton Beam Combined With Anti-VEGF Therapy for Exudative AMD

Sponsor: University of California, Davis

Purpose: To test the hypothesis that proton beam irradiation combined with intravitreal anti-VEGF therapy is safe and potentially more effective than intravitreal anti-VEGF therapy alone in eyes with exudative AMD

Design: Randomized, Placebo Control, Safety/Efficacy, Parallel Assignment, Double-blind

Number of Patients: 45

Inclusion Criteria: VA 20/40 to 20/400; lesion size <12 DA; submacular hemorrhage <75% of total lesion and not involving foveal center; submacular fibrosis <25% of total lesion

Exclusion Criteria: Previous treatment with photodynamic therapy or thermal laser; anti-VEGF therapy within 6 weeks; intravitreal or sub-Tenon’s Kenalog within 6 months

Information: (916) 734-6074

Study: Addition of 20 mg/Day Zeaxanthin to Triple Therapy Treatment Options for AMD

Sponsor: The Retina Center of St. Louis County, P.C./ZeaVision, Inc.

Purpose: To evaluate whether 20 mg per day of oral zeaxanthin as a supplement to patients with CNV and exudative AMD undergoing combination therapy with bevacizumab, dexamethasone and PDT laser photocoagulation improves outcomes

Design: Observational, Case Control, Retrospective

Number of Patients: 200

Inclusion Criteria: Subjects must have AMD with a CNV membrane either classic or occult in at least one eye; preoperative BCVA equal to or greater than 19 letters on the ETDRS diabetic retinopathy study chart (20/400 Snellen); media clarity, pupillary dilation and subject cooperation sufficient for accurate OCT and angiographic assessment

Exclusion Criteria: Retinal disease not AMD; any presumed ocular infections, ie, bacterial, viral, parasitic, or fungal in either eye at the baseline visit; contraindication to pupillary dilation in either eye

Information: rjolk@retina-stl.com

WET AMD

Study: Proton Radiation Therapy for Macular Degeneration

Sponsor: University of Florida

Purpose: To determine if proton radiation therapy can provide effective and safe treatment for subfoveal neovascularization membrane

Design: Interventional, Safety, Single Group, Open Label

Number of Patients: 10

Inclusion Criteria: Patients with subfoveal neovascular membranes identified on fluorescein angiography; VA (best-corrected vision) 20/200 or worse in affected eye; patients must have had prior treatment for macular degeneration with Avastin (bevacizumab) or Lucentis (ranibizumab)

Exclusion Criteria: History of diabetes

Information: (877) 686-6009

Study: A Phase 3 Safety and Efficacy Study of Fovista (E10030) Intravitreous Administration in Combination With Lucentis Compared to Lucentis Monotherapy

Sponsor: Ophthotech Corp.

Purpose: To evaluate the safety and efficacy of intravitreal administration of Fovista administered in combination with Lucentis compared to Lucentis monotherapy in subjects with subfoveal choroidal neovascularization secondary to AMD

Design: Interventional, Randomized, Safety/Efficacy, Parallel Assignment, Double-blind

Number of Patients: 622

Inclusion Criteria: Subfoveal choroidal neovascularization (CNV) due to AMD with some classic component

Exclusion Criteria: Any prior treatment for AMD in the study eye prior to the Day 1 visit, except oral supplements of vitamins and minerals; any prior intravitreal treatment in the study eye prior to the Day 1 visit, regardless of indication (including intravitreal corticosteroids)

Information: Karen.Lewis@ophthotech.com

Study: PREVENT: Prophylactic Ranibizumab for Exudative Age-related Macular Degeneration

Sponsor: Southern California Desert Retinal Consultants

Purpose: To determine whether quarterly injections of ranibizumab may prevent eyes with dry age-related macular degeneration from progressing to wet age-related macular degeneration

Design: Randomized, Efficacy, Parallel Assignment, Single-blind, Prevention

Number of Patients: 100

Inclusion Criteria: Nonexudative age-related macular degeneration (AMD) in one eye (study eye); history of exudative AMD in one eye only (fellow eye) diagnosed within 5 years of study enrollment

Exclusion Criteria: Presence of ocular conditions with increased risk of choroidal neovascularization (CNVM) or pigment epithelial detachment (PED), including presumed ocular histoplasmosis syndrome (POHS), traumatic choroidal rupture, angioid streaks, pathologic myopia (spherical equivalent of ≥ -8 diopters or axial length of ≥ 25 mm), multifocal choroiditis, macular choroidal nevus, polypoidal choroidal vasculopathy (PCV), idiopathic central serous chorioretinopathy (ICSC), etc.

Information: mlalezary@desertretina.com

Study: EMERGE: Study Evaluating Intravitreal hI-con1™ in Patients With Choroidal Neovascularization Secondary to Age-related Macular Degeneration

Sponsor: Iconic Therapeutics

Purpose: To evaluate the safety, biological activity and pharmacodynamic effect of repeated intravitreal doses of hI-con1 0.3 mg administered as monotherapy and in combination with ranibizumab 0.5 mg compared to ranibizumab 0.5 mg monotherapy in treating patients with choroidal neovascularization (CNV) secondary to age-related macular degeneration

Design: Randomized, Safety/Efficacy, Parallel Assignment, Double-blind

Number of Patients: 90

Inclusion Criteria: Active primary CNV secondary to AMD in the study eye; BCVA of 70 to 24 letters in the study eye

Exclusion Criteria: Monocular patient or patient with a BCVA of 35 or fewer letters (20/200 or worse) in the better seeing eye; any prior treatment of CNV or advanced AMD in the study eye, except for dietary supplements or vitamins; planned or ongoing anti-VEGF treatment in the non-study eye

Information: clinicaltrials@iconictherapeutics.com

Study: DREAM: Regorafenib Eye Drops: Investigation of Efficacy and Safety in Neovascular Age Related Macular Degeneration

Sponsor: Bayer

Purpose: To investigate whether the use of regorafenib eye drops can help patients with neovascular (wet) age-related macular degeneration (wAMD) to see better after 4 weeks and 12 weeks after inclusion into this study

Design: Randomized, Efficacy, Parallel Assignment, Double-blind

Number of Patients: 350

Inclusion Criteria: Active primary subfoveal CNV (choroidal neovascularization) lesions secondary to AMD age-related macular degeneration), including juxtafoveal lesions that affect the fovea as evidenced by FA (fluorescein angiography) in the study eye and reviewed by the central reading center; the area of CNV must occupy at least 50% of total lesion in the study eye, as determined by FA review at the central reading center; evidence of intraretinal and/or subretinal fluid on OCT (optical coherence tomography)

Exclusion Criteria: Concurrent disease in the study eye, other than AMD (eg, corneal diseases and dystrophies, conjunctival diseases, eyelid abnormalities, or any other diseases of the cornea and macula, or optic nerve abnormality) that could compromise visual acuity, likely require medical or surgical intervention during the study period, would limit the potential to gain or lose vision during study treatment, or could otherwise confound interpretation of the results; total lesion size (including neovascularization, scar, blood) >12 disc areas (30.5 mm²) as assessed by FA; only one functional eye, even if that eye is otherwise eligible for the study

Information: clinical-trials-contact@bayerhealthcare.com

Study: Efficacy and Safety of RTH258 Versus Aflibercept

Sponsor: Alcon

Purpose: To compare RTH258 ophthalmic solution for intravitreal (IVT) injection at two dosage levels to aflibercept solution for IVT injection (2 mg) in subjects with untreated active choroidal neovascularization (CNV) secondary to age-related macular degeneration (AMD) in the study eye

Design: Randomized, Parallel Assignment, Double-blind

Number of Patients: 1,600

Inclusion Criteria: Active CNV lesions secondary to AMD in the study eye; intra and/or subretinal fluid affecting the central subfield of the study eye; BCVA between 78 and 23 letters, inclusive, in the study eye using Early Treatment Diabetic Retinopathy Study (ETDRS) testing

Exclusion Criteria: Any active intraocular or periocular infection or active intraocular inflammation in either eye; fibrosis or geographic atrophy; any approved or investigational treatment for neovascular AMD (other than vitamin supplements) in the study eye at any time; any history or evidence of a concurrent intraocular condition in the study eye that, in the judgment of the Investigator, could require either medical or surgical intervention during the course of the study to prevent or treat visual loss

Information: alcon.medinfo@alcon.com

Study: LHA510 Proof-of-Concept Study as a Maintenance Therapy for Patients With Age-Related Macular Degeneration

Sponsor: Alcon

Purpose: To evaluate the efficacy of 12 successive weeks of topically administered LHA510 compared to vehicle in reducing the number of patients requiring intravitreal (IVT) anti-vascular endothelial growth factor (VEGF) therapy (Lucentis) for recurrence of active choroidal neovascularization (CNV)

Design: Randomized, Efficacy, Parallel Assignment, Double-blind

Number of Patients: 60

Inclusion Criteria: Wet AMD; active CNV lesion due to AMD in the study eye; BCVA between 75-35 letters, inclusive in the study eye; BCVA 20 letters in the fellow eye

Exclusion Criteria: Any active ocular or periocular infection or intraocular inflammation; history of visual impairing central keratitis or endophthalmitis in the study eye; received >25 IVT injections of anti-VEGF therapy in the study eye; initial diagnosis of wet AMD in the study eye >3 years prior to screening visit; current or history of macular or retinal disease other than wet AMD in the study eye

Information: alcon.medinfo@alcon.com

Study: Sirolimus vs AntiVEGF for Wet AMD

Sponsor: Raj K. Maturi, MD, PC

Purpose: To determine safety and efficacy of intravitreal injections of Sirolimus in subjects with wet age-related macular degeneration (wet AMD) with persistent intraretinal or subretinal edema due to neovascular AMD despite previous anti-VEGF treatment

Design: Randomized, Safety/Efficacy, Parallel Assignment, Single-blind

Number of Patients: 30

Inclusion Criteria: Best corrected visual acuity of 5-65, inclusive, in study eye; presence of choroid neovascularization secondary to AMD; persistent edema despite at least 3 previous intravitreal anti-VEGF injections in 5 months

Exclusion Criteria: Greater than 100 micron decrease in central subfield thickness on OCT since last standard of care visit; history of major ophthalmic surgery in the study eye in the past 3 months; history of significant ocular disease or condition other than exudative AMD

Information: rmaturi@gmail.com

Study: Study of Intravitreal (IVT) REGN910-3 and IVT REGN910 in Patients With Either Neovascular (“Wet”) Age Related Macular Degeneration (AMD) or Diabetic Macular Edema (DME)

Sponsor: Regeneron

Purpose: To investigatethe safety and tolerability of intravitreal (IVT) REGN910-3 and IVT REGN910 in patients with neovascular age-related macular degeneration (AMD), and separately in patients with diabetic macular edema (DME)

Design: Nonrandomized, Safety/Efficacy, Single Group, Open Label

Inclusion Criteria: Active subfoveal choroidal neovascularization (CNV) secondary to AMD, including juxtafoveal lesions that affect the fovea as evidenced by FA or OCT in the study eye, as determined by the investigator

Exclusion Criteria: Evidence of choroidal neovascularization (CNV) due to any cause other than AMD in either eye; evidence of diabetic retinopathy (DR) or DME in either eye

Information: clinicaltrials@regeneron.com

Study: VAPOR1: A Safety and Efficacy Study of DE-120 Injectable Solution for Age-related Macular Degeneration

Sponsor: Santen Inc.

Purpose: To evaluate the safety and efficacy of intravitreal (IVT) administration of DE-120 in subjects with treatment-naive active subfoveal choroidal neovascularization (CNV) secondary to age-related macular degeneration

Design: Randomized, Safety/Efficacy, Parallel Assignment, Open Label

Number of Patients: 30

Inclusion Criteria: Diagnosis of active CNV secondary to wet AMD, with some subfoveal component in the study eye; no evidence of subfoveal fibrosis or subfoveal RPE atrophy in the study eye; at least one lesion in the study eye that meets minimal pathology criteria; best corrected visual acuity of 70 to 25 ETDRS letters in the study eye

Exclusion Criteria: Aphakic or has an anterior chamber intraocular lens in the study eye; received prior treatment with anti-VEGF, intravitreal corticosteroids or photodynamic therapy in the study eye; uncontrolled glaucoma despite anti-glaucoma therapy in the study eye; evidence of any ocular disease other than AMD in the study eye that may confound the outcome of the study; history of vitrectomy in the study eye

Information: clinicaltrials@santeninc.com

WET AMD

Study: ASAP II: Assessment of Safety, Tolerability and Pharmacokinetics of Intravitreal APL-2 for Patients With Wet AMD

Sponsor: Apellis Pharmaceuticals

Purpose: To provide initial safety, tolerability and pharmacokinetics information of intravitreal administration of APL-2 in order to support further development into larger Phase II studies for treatment of patients with AMD

Design: Nonrandomized, Safety, Single Group, Open Label

Number of Patients: 9

Inclusion Criteria: The presence of an active choroidal neovascular lesion secondary to AMD; on treatment with anti-VEGF therapy (Lucentis®, Eylea® or Avastin®); must have received at least 3 anti-VEGF treatments over the 26-week period prior to screening (Screening Visit); evidence that the macular fluid has responded to anti-VEGF in the past based on OCT in the opinion of the PI

Exclusion Criteria: Choroidal neovascularization associated with other ocular diseases such as pathologic myopia, ocular histoplasmosis or posterior uveitis, etc.; decreased vision due to retinal disease not attributable to choroidal neovascularization, such as nonexudative forms of AMD, geographic atrophy, inherited retinal dystrophy, uveitis or epiretinal membrane, a vitelliform-like lesion of the outer retina (e.g., as in pattern dystrophies or basal laminar drusen), idiopathic parafoveal telangiectasis, or central serous retinopathy

Information: federico@apellis.com

Study: An 18 Month Phase 2a Open Label, Randomized Study of Avastin®, Lucentis®, or Eylea® (Anti-VEGF Therapy) Administered in Combination With Fovista® (Anti-PDGF BB Pegylated Aptamer)

Sponsor: Ophthotech Corporation

Purpose: To evaluate the safety of intravitreal (IVT) Fovista® administered in combination with anti-VEGF therapy

Design: Randomized, Safety, Parallel Assignment, Open Label

Number of Patients: 60

Inclusion Criteria: Active subfoveal choroidal neovascularization (CNV) due to AMD

Exclusion Criteria: Any intraocular surgery or thermal laser within three (3) months of trial entry. Any prior thermal laser in the macular region, regardless of indication; subjects with subfoveal scar or subfoveal atrophy; any ocular or periocular infection in the past twelve (12) weeks; history of any of the following conditions or procedures in the study eye: rhegmatogenous retinal detachment, pars plana vitrectomy, filtering surgery (e.g. trabeculectomy), glaucoma drainage device, corneal transplant.

Information: jeff.nau@ophthotech.com

Study: X-82 to Treat Age-related Macular Degeneration

Sponsor: Tyrogenex

Purpose: To evaluate the safety and efficacy of X-82 in the treatment of vision loss due to wet AMD

Design: Randomized, Safety/Efficacy, Single Group, Double-blind

Number of Patients: 132

Inclusion Criteria: Participants must have wet AMD which has been diagnosed and treated with anti-VEGF in one or both eyes for at least 1 year prior to joining the study and has required at least three prior injections of Eylea at intervals of not greater than 6 weeks for the past three injections in the eye that is selected to be the study eye; must have demonstrated the ability to achieve a dry macula in the study eye 14 days following an injection of Eylea at Screening Visit 1; Early Treatment Diabetic Retinopathy (ETDRS) Best Corrected Visual Acuity (BCVA) of 20 letters (20/400) or better in both eyes

Exclusion Criteria: Previous vitrectomy to the study eye; choroidal neovascularization (CNV) due to causes other than AMD; proliferative diabetic retinopathy in either eye

Information: denis@tyrogenex.com

DIABETIC MACULAR EDEMA

Study: Phase II Combination Steroid and Anti-VEGF for Persistent DME

Sponsor: DRCRnet

Purpose: To assess whether the addition of steroid to an anti-VEGF treatment regimen in pseudophakic eyes has beneficial effect short-term in eyes with persistent DME and vision impairment despite previous anti-VEGF therapy, compared with anti-VEGF therapy alone

Design: Interventional, Randomized, Safety/Efficacy, Parallel Assignment, Double-blind

Number of Patients: 125

Inclusion Criteria: At least 6 injections of anti-VEGF drug (ranibizumab, bevacizumab, or aflibercept) within the prior 36 weeks; VA letter score in study eye ≤ 78 and ≥24 (approximate Snellen equivalent 20/32 to 20/320); on clinical exam definite retinal thickening due to DME involving the center of the macula

Exclusion Criteria: An ocular condition is present such that, in the opinion of the investigator, VA loss would not improve from resolution of macular edema, an ocular condition is present (other than DME) that, in the opinion of the investigator, might affect macular edema or alter VA during the course of the study; substantial posterior capsule opacity that, in the opinion of the investigator, is likely to be decreasing visual acuity by 3 lines or more

Information: http://drcrnet.jaeb.org/ViewPage.aspx?PageName=Home

Study: A Phase 2, Multi-Center Study To Compare The Efficacy And Safety Of A Chemokine CCR2/5 Receptor Antagonist With Ranibizumab In Adults With Diabetic Macular Edema

Sponsor: Pfizer

Purpose: To provide an alternative mechanism to treat DME

Design: Interventional, Randomized, Safety/Efficacy, Parallel Assignment, Double-blind

Number of Patients: 200

Inclusion Criteria: Patients with diabetes mellitus (Type 1 or Type 2) showing DME; reduced VA resulting from retinal thickening

Exclusion Criteria: Severe impaired renal function; any intraocular condition or previous surgery in either eye that would likely require medical or surgical intervention during the study

Information: https://trialinfoemail.pfizer.com/pages/landing.aspx

Study: ROTATE: Ranibizumab For Persistent DME After Bevacizumab

Sponsor: Southeast Retina Center/Genentech

Purpose: To determine the safety and efficacy of intravitreally administered 0.3 mg ranibizumab in subjects with persistent DME after recent and frequent bevacizumab (at least 2 bevacizumab intravitreal injections within 2 months prior to enrollment and at least 6 bevacizumab injections within 9 months)

Design: Interventional, Randomized, Safety/Efficacy, Parallel Assignment, Open Label

Number of Patients: 30

Inclusion Criteria: Central-involved DME in study eye; definite retinal thickening due to DME involving the center of the macula

Exclusion Criteria: Known allergy to ranibizumab; acute cardiovascular event requiring hospitalization within the past 3 months; systemic anti-VEGF or pro-VEGF treatment within 3 months prior to randomization or anticipated use

Information: dmarcus@southeastretina.com

Study: OPERA: Ozurdex for Diabetic Macular Edema Treated With Pars Plana vitrEctomy and Membrane Removal

Sponsor: Cleveland Clinic/Allergan

Purpose: To examine the use of the dexamethasone implant (Ozurdex) in patients with DME associated with an epiretinal or preretinal membrane requiring surgical intervention

Design: Interventional, Single Group Assignment, Open Label

Number of Patients: 30

Inclusion Criteria: Patients who are undergoing pars plana vitrectomy for: epiretinal membrane/vitreomacular traction or DME; patients with macular edema as measured by OCT (at least 250 µm central subfoveal thickness)

Exclusion Criteria: History of active inflammatory eye disease (uveitis) (within 3 months); history of ocular malignancy and/or ocular/orbital irradiation; history of recent retinal vein occlusion (within 6 months)

Information: srivass2@ccf.org

Study: Protocol V: Treatment for CI-DME in Eyes With Very Good VA Study

Sponsor: Diabetic Retinopathy Clinical Research Network/Genentech

Purpose: To compare the percentage of eyes that have lost at least 5 letters of VA at 2 years compared with baseline mean VA in eyes with central-involved DME and good VA

Design: Randomized, Interventional, Safety/Efficacy, Parallel Assignment, Single-blind

Number of Patients: 702

Inclusion Criteria: Best corrected E-ETDRS VA letter score ≥ 79 (approximate Snellen equivalent 20/25 or better) at two consecutive visits within 1 to 28 days; on clinical exam, definite retinal thickening

Exclusion Criteria: Macular edema is due to a cause other than DME

Information: drcrnet@jaeb.org

Study: REACT: Safety and Efficacy of Ranibizumab for DME

Sponsor: Cleveland Clinic/Genentech

Purpose: To assess the ocular and systemic adverse events of ranibizumab (Lucentis) for DME following previous treatment with intravitreal bevacizumab (Avastin)

Design: Safety/Efficacy, Single Group, Single-blind, Treatment

Number of Patients: 30

Inclusion Criteria: ETDRS best-corrected visual acuity of 20/25 to 20/320 in the study eye; willing, committed, and able to return for all clinic visits and complete all study related procedures; at least 6 previous bevacizumab injections for DME in the last 12 months

Exclusion Criteria: Intravitreal steroid or periocular steroid treatment within 3 months of study entry; focal/grid laser photocoagulation treatment within 3 months

Information: DASTOLK@ccf.org

Study: PROMISE: Prevention of Macular Edema In Patients With Diabetic Retinopathy Undergoing Cataract Surgery

Sponsor: Cleveland Clinic/Regeneron

Purpose: To determine the safety and efficacy of intravitreal Aflibercept (Eylea) injection in patients with diabetic retinopathy in the prevention of macular edema following cataract surgery

Design: Randomized, Safety/Efficacy, Single Group, Single-blind, Prevention

Number of Patients: 30

Inclusion Criteria: Non-proliferative diabetic retinopathy (mild, moderate, or severe) or inactive proliferative disease

Exclusion Criteria: Signs of vitreomacular traction or epiretinal membrane in the study eye as detected by reading center or investigator

Information: DASTOLK@ccf.org

Study: A Study of MTP-131 Topical Ophthalmic Solution in Subjects With DME

Sponsor: Stealth Peptides, Inc.

Purpose: To determine the effects of topical ocular administration of low dose or high dose MTP-131 given twice a day in subjects with DME

Design: Nonrandomized, Safety/Efficacy, Open Label

Number of Patients: 21

Inclusion Criteria: Central subfield thickness (CST) ≥325 microns as measured by SD-OCT at Screening and Baseline Visits; BCVA (ETDRS) no better than 20/25

Exclusion Criteria: Any ocular condition in the study eye that would prevent improvement in VA

Information: (617) 600-6888

Study: A Phase 1, Open-Label Study of Teprotumumab in Patients With Diabetic Macular Edema

Sponsor: River vision Development Corp.

Purpose: To evaluate the safety of teprotumumab in patients with diabetic macular edema

Design: Safety, Single Group, Open Label, Treatment

Number of Patients: 10

Inclusion Criteria: Clinically significant DME of less than 12 months duration; non-proliferative diabetic retinopathy of moderate severity

Exclusion Criteria: Systemic anti-VEGF treatment within four months prior to enrollment; history of pan retinal photocoagulation within four months prior to enrollment

Information: kcgabriel2@verizon.net

DIABETIC MACULAR EDEMA

Study: A Phase 2 Randomized, Controlled, Double-Masked, Multicenter Clinical Trial Designed to Evaluate the Safety and Exploratory Efficacy of Luminate (ALG-1001) as Compared to Avastin and Focal Laser Photocoagulation in the Treatment of DME

Sponsor: Allegro Ophthalmics

Purpose: To evaluate the safety and efficacy of Luminate compared to Avastin and focal laser in the treatment of DME

Design: Randomized, Safety/Efficacy, Parallel Assignment, Double-blind

Number of Patients: 150

Inclusion Criteria: BCVA of 20/50 to 20/320 ETDRS equivalent (65 letters to 23 letters) in the study eye, with BCVA decrement primarily attributable to DME; treatment naïve

Exclusion Criteria: Active proliferative diabetic retinopathy (PDR) in the study eye such as NVE, NVD, vitreous hemorrhage, or neovascular glaucoma; uncontrolled hypertension defined as systolic >180 mmHg or > 160 mmHg on 2 consecutive measurements or diastolic > 100 mmHg on optimal medical regimen

Information: (949) 940-8130

Study: VIDI: A Study to Evaluate ASP8232 in Reducing Central Retinal Thickness in Subjects With DME

Sponsor: Astellas Pharma Europe BV

Purpose: To evaluate efficacy and safety of ASP8232 in subjects with DME

Design: Randomized, Safety/Efficacy, Parallel Assignment, Double-blind

Number of Patients: 84

Inclusion Criteria: Subject has definite retinal thickening due to diffuse DME involving the central macula based on evaluating investigator’s clinical evaluation and demonstrated by SD-OCT

Exclusion Criteria: Subject’s study eye has macular edema considered to be due to a cause other than DME; subject’s study eye has a decrease in BCVA

Information: Astellas.registration@astellas.com

Study: DIME: Dexamethasone Intravitreal Implant for the Treatment of Persistent Diabetic Macular Edema

Sponsor: California Retina Consultants

Purpose: To compare the effectiveness of using a dexamethasone steroid implant versus monthly intravitreal anti-VEGF injections for research participants with persistent diabetic macular edema

Design: Randomized, Efficacy, Parallel Assignment, Open Label

Number of Patients: 40

Inclusion Criteria: Clinical evidence of retinal thickening due to macular edema involving the center of the macula associated with diabetic retinopathy; previous history of anti-vegf treatment for diabetic macular edema (DME) with documented incomplete resolution of central subfield thickening by spectral-domain optical coherence tomography (SDOCT). At least 4 intravitreal anti-vegf injections within the past six months prior to the baseline study visit are required for eligibility; central diabetic macular edema present on clinical examination and SDOCT testing with central 1 mm subfield thickness greater than 300 microns as measured on SDOCT at the baseline visit.

Exclusion Criteria: Evidence of vitreoretinal interface abnormality after ocular exam or OCT that may be contributing to the macular edema; an eye that, in the investigator’s opinion, has no chance of improving in visual acuity following resolution of macular edema (e.g. presence of subretinal fibrosis or geographic atrophy); presence of another ocular condition that may affect the visual acuity or macular edema during the course of the study (e.g. AMD, uveitis, Irvine-Gass); evidence of active neovascularization of the iris or retina

Information: sarahf@californiaretina.com

Study: PALADIN: Phase 4 IOP Signals Associated With ILUVIEN

Sponsor: Alimera Sciences

Purpose: To assess the safety in patients treated with ILUVIEN, with primary focus on IOP

Design: Nonrandomized, Safety, Single Group, Open Label

Number of Patients: 300

Inclusion Criteria: Patients who are eligible for treatment with ILUVIEN based on the Prescribing Information

Information: kathleen.billman@alimerasciences.com

RETINAL VEIN OCCLUSION

Study: Intra-arterial Thrombolysis for Severe Recent CRVO

Sponsor: Weill Medical College of Cornell University

Purpose: To determine whether thrombolysis can improve visual acuity and prevent the long-term complications of CRVO

Design: Interventional, Safety/Efficacy, Single Group Assignment, Open Label, Treatment

Number of Patients: 5

Inclusion Criteria: Severe CRVO diagnosed on presence of relative afferent papillary defect (RAPD) or visual acuity of 20/200 or worse; symptom onset within 2 weeks

Exclusion Criteria: Contraindication to thrombolysis: active or recent (1 month) internal bleeding, cerebrovascular accident, major organ surgery, major trauma; intracranial neoplasm or vascular malformation, known bleeding diathesis, severe uncontrolled arterial hypertension

Information: kas2004@med.cornell.edu

Study: Open Label Study to Assess the Efficacy and Safety of AKB-9778 in Subjects With Macular Edema Due to RVO

Sponsor: Aerpio Therapeutics

Purpose: To assess the efficacy and safety of subcutaneous 15mg AKB-9778 administered twice daily for 84 days in subjects with macular edema due to RVO

Design: Safety/Efficacy, Single Group, Open Label

Number of Patients: 20

Inclusion Criteria: Definite retinal thickening due to RVO involving the central macula based on Investigator’s clinical evaluation and demonstrated by SD-OCT; mean central subfield thickness of at least 325 µm by SD-OCT with presence of intraretinal fluid; ETDRS BCVA letter score ≤ 76 and ≥ 24; decrease in vision determined to be primarily the result of macular edema due to RVO and not due to other causes

Exclusion Criteria: Macular edema is considered to be due to a cause other than RVO; any other ocular disease that may cause substantial reduction in visual acuity, including iris neovascularization, retinal detachment, epiretinal membrane, vitreous hemorrhage or fibrosis, ocular inflammation (uveitis), retinal inflammatory, infectious disease

Information: jbonfrisco@aerpio.com

Study: Minocycline to Treat Retinal Vein Occlusion

Sponsor: National Eye Institute

Purpose: To test the safety and effectiveness of minocycline as a treatment for RVO

Design: Randomized, Safety/Efficacy, Parallel Assignment, Double-blind

Number of Patients: 40

Inclusion Criteria: Evidence of definite retinal thickening due to RVO involving the center of the macula

Exclusion Criteria: Macular edema related to cataract extraction, or clinical examination and/or OCT suggest that vitreoretinal interface disease is the primary cause of the macular edema, or clinical examination

Information: meg.gordon@nih.gov

Study: ORION: Ozurdex vs Ranibizumab vs Combination for Central Retinal Vein Occlusion

Sponsor: Valley Retina Institute

Purpose: To determine the safety and effectiveness of treating CRVO-associated macular edema with a combination of 0.7 mg of Ozurdex and 0.5 mg Lucentis

Design: Randomized, Safety/Efficacy, Parallel Assignment, Single-blind

Number of Patients: 45

Inclusion Criteria: Foveal center involved macular edema secondary to central retinal vein occlusion diagnosed within 12 months

Exclusion Criteria: History of vitreoretinal surgery in the study eye or anticipated within 12 months of Day 1; bilateral Central retinal vein occlusion

Information: dgarcia@vritx.com

Study: Effect of Ozurdex 0.7 mg on Improvement of Efficacy of Bevacizumab for Central Retinal Vein Occlusion

Sponsor: Texas Retina

Purpose: To determine if the addition of Ozurdex to Avastin eye injections reduces the need for repeat bevacizumab eye injections in patients with nonischemic CRVO

Design: Safety/Efficacy, Parallel Assignment, Single-blind

Number of Patients: 68

Exclusion Criteria: Any systemic disease or clinical evidence of any condition which would make the subject unsuitable for the study or confound the study results

Information: (732) 797-3984

Study: Clinical Trial of Autologous Intravitreal Bone-marrow CD34+ Stem Cells for Retinopathy

Sponsor: University of California, Davis

Purpose: To determine whether it would be safe and feasible to inject CD34+ stem cells from bone marrow into the eye as treatment for patients who are irreversibly blind from various retinal conditions

Design: Safety/Efficacy, Single Group, Open Label

Number of Patients: 15

Inclusion Criteria: VA 20/200 to CF; duration of vision loss > 3 months; vision loss from AMD, retinitis pigmentosa, RVO, or DR

Exclusion Criteria: Allergy to fluorescein dye; other retinal or optic nerve disease

Information: marisa.salvador@ucdmc.ucdavis.edu

Study: SCORE2: Study of Comparative Treatments for RVO 2

Sponsor: The EMMES Corp./NEI/Hershey Medical Center/Univ. Wisconsin

Purpose: To determine if bevacizumab is noninferior to aflibercept for the treatment of macular edema associated with central retinal vein occlusion, with the primary outcome of VA measured at Month 6

Design: Randomized, Efficacy, Parallel Assignment, Single-blind

Number of Patients: 360

Inclusion Criteria: Must have center-involved macular edema secondary to central retinal vein occlusion

Exclusion Criteria: Examination evidence of vitreoretinal interface disease

Information: pvanveldhuisen@emmes.com

Study: Ozurdex With Rescue Lucentis for Treating Macular Edema Secondary to Retinal Vein Occlusion

Sponsor: Brian Burke, MPH

Purpose: To compare dexamethasone implant with rescue intravitreal ranibizumab to monthly intravitreal ranibizumab for the treatment of macular edema secondary to BRVO or CRVO

Design: Randomized, Efficacy, Parallel Assignment, Open Label

Number of Patients: 30

Inclusion Criteria: RVO diagnosed within two weeks of symptom onset; BCVA on initial presentation between 20/40 and 20/320

Exclusion Criteria: Patients with any history of prior intravitreal dexamethasone or anti-VEGF or grid laser; patients with DR or AMD

Information: research@midatlanticretina.com

Study: TANZANITE: Suprachoroidal Injection of Triamcinolone Acetonide With IVT Aflibercept in Subjects With Macular Edema Following RVO

Sponsor: Clearside Biomedical, Inc.

Purpose: To evaluate the safety and efficacy of a single suprachoroidal injection of CLS-TA, triamcinolone acetonide injectable suspension, given along with an intravitreal (IVT) injection of aflibercept compared to IVT aflibercept alone in subjects with RVO

Design: Randomized, Safety/Efficacy, Parallel Assignment, Double-blind

Number of Patients: 40

Inclusion Criteria: Diagnosis of macular edema following RVO; history of ME ≤ 12 months; 20-70 letters inclusive BCVA

Exclusion Criteria: IVT injection of anti-VEGF for RVO in the study eye

Information: michelle.widmann@clearsidebio.com

UVEITIS

Study: Safety and Efficacy Study of Gevokizumab to Treat Active Non-infectious Uveitis

Sponsor: Xoma, LLC

Purpose: To evaluate the efficacy of gevokizumab in the treatment of active non-infectious intermediate, posterior, or panuveitis

Design: Randomized, Safety/Efficacy, Parallel Assignment, Double-blind

Number of Patients: 300

Inclusion Criteria: Diagnosis of non-infectious intermediate, posterior, or panuveitis in at least one eye; active uveitic disease in at least one eye

Exclusion Criteria: Infectious uveitis and masquerade syndromes; isolated anterior uveitis; contraindication to mydriatics; history of allergic or anaphylactic reactions to monoclonal antibodies

Information: (510) 204-7515

Study: SAKURA: Study Assessing Double-masked Uveitis Treatment

Sponsor: Santen Inc.

Purpose: To evaluate the safety and efficacy of intravitreal injections of DE-109 ophthalmic solution

Design: Randomized, Safety/Efficacy, Parallel Assignment, Double-blind

Number of Patients: 600

Inclusion Criteria: Meet ETDRS BCVA; confirmed diagnosis of active uveitis

Exclusion Criteria: Uveitis of infectious etiology; suspected/confirmed central nervous system or ocular lymphoma; primary diagnosis of anterior uveitis

Information: clinicaltrials@santeninc.com

Study: FAST: Methotrexate and Mycophenolate Mofetil

Sponsor: University of California, San Francisco

Purpose: To establish which immunosuppressive therapy, methotrexate or mycophenolate mofetil, is more effective as a first-line, corticosteroid-sparing agent for the treatment of non-infectious uveitis in a block-randomized, observer-masked, comparative effectiveness trial

Design: Randomized, Efficacy, Crossover Assignment, Double-blind

Number of Patients: 216

Inclusion Criteria: Historical non-infectious intermediate, anterior and intermediate, posterior or panuveitis in at least one eye; active inflammation within the last 180 days

Exclusion Criteria: Any infectious cause of uveitis; prior use of any immunosuppressive drug other than prednisone; media opacity (such as cataract and/or corneal scar) and/or extensive posterior synechiae

Information: erica.browne@ucsf.edu

Study: Safety,Tolerability and Efficacy of Intravitreal LFG316 in Patients With Active Non-infectious Intermediate-, posterior- or Panuveitis

Sponsor: Novartis

Purpose: To assess the safety and efficacy of LFG316 in active, non-infectious intermediate-, posterior-, or panuveitis

Design: Randomized, Safety/Efficacy, Parallel Assignment, Open Label

Number of Patients: 24

Inclusion Criteria: Male or female patients 18 years or older with active uveitic disease (flare) in study eye; visual acuity (ETDRS method) of 20 letters (20/400 Snellen equivalent) or better in the study eye

Exclusion Criteria: Any biologic immunosuppressive agent given via intravitreal, intravenous or subcutaneous route within 4-12 months depending on the agent; any intraocular surgery, intravitreal injection, periocular injection, or laser photocoagulation to the study eye within 90 days prior to dosing

Information: (888) 669-6682

Study: POINT: PeriOcular and INTravitreal Corticosteroids for Uveitic Macular Edema Trial

Sponsor: JHSPH Center for Clinical Trials/NEI

Purpose: To evaluate the relative efficacy of three commonly utilized regional corticosteroids for the regional treatment of uveitic macular edema: periocular triamcinolone acetonide; intravitreal triamcinolone acetonide; intravitreal dexamethasone implant

Design: Randomized, Safety/Efficacy, Parallel Assignment, Open Label

Number of Patients: 267

Inclusion Criteria: Non-infectious anterior, intermediate, posterior or panuveitis; either active or inactive uveitis is acceptable; macular edema (ME) defined as the presence of central subfield macular thickness greater than the normal range for the OCT machine being used, regardless of the presence of cysts, as assessed by study ophthalmologist; best corrected visual acuity (BCVA) of 20/40 to 5/200; baseline intraocular pressure > 5 mm Hg and ≤ 21 mm Hg (current use of 2 or fewer intraocular pressure-lowering medications and/or prior glaucoma surgery are acceptable)

Exclusion Criteria: History of severe glaucoma as defined by optic nerve damage (cup/disc ratio of ≥ 0.9 or any notching of optic nerve to the rim); media opacity causing inability to assess fundus or perform OCT; presence of an epiretinal membrane noted clinically or by OCT that per the judgment of study ophthalmologist may be significant enough to limit improvement of ME (i.e., causing substantial wrinkling of the retinal surface); presence of silicone oil

Information: jholbro1@jhu.edu

NO LONGER RECRUITING

Study: Treatment-Resistant Neovascular Age-Related Macular Degeneration

Sponsor: Washington U. School of Medicine

Information: pistoriuss@vision.wustl.edu

Study: A Phase I Single Ascending Dose Study of the Intravitreal Plasma Kallikrein Inhibitor KVD001 in Subjects With DME

Sponsor: KalVista Pharmaceuticals/JDRF

Information: www.kalvista.com

Study: SATURN: Phase II Study to Analyze Sarilumab in Non-Infectious Uveitis

Sponsor: Sanofi

Information: Contact-Us@sanofi.com